All Stories

  1. AlphaFold2-based prediction of the co-condensation propensity of proteins
  2. Modulation of α-synuclein in vitro aggregation kinetics by its alternative splice isoforms
  3. Multiomic prediction of therapeutic targets for human diseases associated with protein phase separation
  4. Formation of amyloid loops in brain tissues is controlled by the flexibility of protofibril chains
  5. Spontaneous nucleation and fast aggregate-dependent proliferation of α-synuclein aggregates within liquid condensates at neutral pH
  6. Widespread occurrence of the droplet state of proteins in the human proteome
  7. Rational design of a conformation-specific antibody for the quantification of Aβ oligomers
  8. Sequence-based prediction of protein binding mode landscapes
  9. Chris Dobson (1949–2019)
  10. Widespread remodeling of proteome solubility in response to different protein homeostasis stresses
  11. The N-terminal Acetylation of α-Synuclein Changes the Affinity for Lipid Membranes but not the Structural Properties of the Bound State
  12. Dynamics of oligomer populations formed during the aggregation of Alzheimer’s Aβ42 peptide
  13. Proteome-wide observation of the phenomenon of life on the edge of solubility
  14. Determination of a Structural Ensemble Representing the Dynamics of a G-Quadruplex DNA
  15. Million-fold sensitivity enhancement in proteopathic seed amplification assays for biospecimens by Hofmeister ion comparisons
  16. Bacterial production and direct functional screening of expanded molecular libraries for discovering inhibitors of protein aggregation
  17. Probing the dynamic stalk region of the ribosome using solution NMR
  18. Differential Interactome and Innate Immune Response Activation of Two Structurally Distinct Misfolded Protein Oligomers
  19. Determination of protein structural ensembles using cryo-electron microscopy
  20. Expression of the amyloid-β peptide in a single pair of C. elegans sensory neurons modulates the associated behavioural response
  21. Probing the Origin of the Toxicity of Oligomeric Aggregates of α-Synuclein with Antibodies
  22. Identifying A- and P-site locations on ribosome-protected mRNA fragments using Integer Programming
  23. The free energy landscape of the oncogene protein E7 of human papillomavirus type 16 reveals a complex interplay between ordered and disordered regions
  24. Secondary nucleation and elongation occur at different sites on Alzheimer’s amyloid-β aggregates
  25. A method of predicting the in vitro fibril formation propensity of Aβ40 mutants based on their inclusion body levels in E. coli
  26. Atomic force microscopy for single molecule characterisation of protein aggregation
  27. A superposition free method for protein conformational ensemble analyses and local clustering based on a differential geometry representation of backbone
  28. Trodusquemine enhances Aβ42 aggregation but suppresses its toxicity by displacing oligomers from cell membranes
  29. Effects of α-tubulin acetylation on microtubule structure and stability
  30. Chemical and mechanistic analysis of photodynamic inhibition of Alzheimer's β-amyloid aggregation
  31. Bayesian Weighing of Electron Cryo-Microscopy Data for Integrative Structural Modeling
  32. A tau homeostasis signature is linked with the cellular and regional vulnerability of excitatory neurons to tau pathology
  33. Identifying A- and P-site locations on ribosome-protected mRNA fragments using Integer Programming
  34. In vitro and in silico assessment of the developability of a designed monoclonal antibody library
  35. Determination of Structural Ensembles of Proteins: Restraining vs Reweighting
  36. Automated Behavioral Analysis of Large C. elegans Populations Using a Wide Field-of-view Tracking Platform
  37. SAR by kinetics for drug discovery in protein misfolding diseases
  38. Microfluidic deposition for resolving single-molecule protein architecture and heterogeneity
  39. Intrinsically aggregation-prone proteins form amyloid-like aggregates and contribute to tissue aging in C. elegans
  40. Fast fluorescence lifetime imaging reveals the aggregation processes of α-synuclein and polyglutamine in aging Caenorhabditis elegans
  41. Systematic mapping of free energy landscapes of a growing filamin domain during biosynthesis
  42. Stabilization and Characterization of Cytotoxic Aβ40 Oligomers Isolated from an Aggregation Reaction in the Presence of Zinc Ions
  43. Author Correction: The molecular chaperones DNAJB6 and Hsp70 cooperate to suppress α-synuclein aggregation
  44. Structural Ensemble Modulation upon Small-Molecule Binding to Disordered Proteins
  45. Massively parallel C. elegans tracking provides multi-dimensional fingerprints for phenotypic discovery
  46. Molecular dynamics ensemble refinement of the heterogeneous native state of NCBD using chemical shifts and NOEs
  47. Determination of the conformational states of strychnine using NMR residual dipolar couplings in a tensor-free approach
  48. Exploring the role of post-translational modifications in regulating α-synuclein interactions by studying the effects of phosphorylation on nanobody binding
  49. Multistep Inhibition of α-Synuclein Aggregation and Toxicity in Vitro and in Vivo by Trodusquemine
  50. Reversible inhibition of the ClpP protease via an N-terminal conformational switch
  51. Cooperative Assembly of Hsp70 Subdomain Clusters
  52. A method for partitioning the information contained in a protein sequence between its structure and function
  53. A Rationally Designed Hsp70 Variant Rescues the Aggregation-Associated Toxicity of Human IAPP in Cultured Pancreatic Islet β-Cells
  54. Developing NMR methods for macromolecular machines: Measurement of residual dipolar couplings to probe dynamical regions of the ribosome
  55. Cholesterol catalyses Aβ42 aggregation through a heterogeneous nucleation pathway in the presence of lipid membranes
  56. Chemical Kinetics for Bridging Molecular Mechanisms and Macroscopic Measurements of Amyloid Fibril Formation
  57. Parapred: antibody paratope prediction using convolutional and recurrent neural networks
  58. FUS Phase Separation Is Modulated by a Molecular Chaperone and Methylation of Arginine Cation-π Interactions
  59. Simultaneous Determination of Protein Structure and Dynamics Using Cryo-Electron Microscopy
  60. Molecular determinants of the interaction of EGCG with ordered and disordered proteins
  61. Distinct thermodynamic signatures of oligomer generation in the aggregation of the amyloid-β peptide
  62. Molecular dynamics ensemble refinement of the heterogeneous native state of NCBD using chemical shifts and NOEs
  63. Third generation antibody discovery methods:in silicorational design
  64. Structural differences between toxic and nontoxic HypF-N oligomers
  65. Structural basis of membrane disruption and cellular toxicity by α-synuclein oligomers
  66. Simultaneous Determination of Protein Structure and Dynamics Using Cryo-Electron Microscopy
  67. MobiDB 3.0: more annotations for intrinsic disorder, conformational diversity and interactions in proteins
  68. Delivery of Native Proteins into C. elegans Using a Transduction Protocol Based on Lipid Vesicles
  69. Oxetane Grafts Installed Site-Selectively on Native Disulfides to Enhance Protein Stability and Activity In Vivo
  70. In Vitro and In Silico Activity of Iridoids Against Leishmania ama-zonensis
  71. Influence of Harvest Season and Cultivar on the Variation of Phenolic Compounds Composition and Antioxidant Properties in Vaccinium ashei Leaves
  72. Systematic mapping of the free energy landscapes of a growing immunoglobulin domain identifies a kinetic intermediate associated with co-translational proline isomerization
  73. Paratope Prediction using Convolutional and Recurrent Neural Networks
  74. Sequence Specificity in the Entropy-Driven Binding of a Small Molecule and a Disordered Peptide
  75. The molecular chaperones DNAJB6 and Hsp70 cooperate to suppress α-synuclein aggregation
  76. Rapid and accurate in silico solubility screening of a monoclonal antibody library
  77. Monomeric and fibrillar α-synuclein exert opposite effects on the catalytic cycle that promotes the proliferation of Aβ42 aggregates
  78. Nanobodies raised against monomeric ɑ-synuclein inhibit fibril formation and destabilize toxic oligomeric species
  79. Protein homeostasis of a metastable subproteome associated with Alzheimer’s disease
  80. Methods of probing the interactions between small molecules and disordered proteins
  81. Amyloid-like Fibrils from an α-Helical Transmembrane Protein
  82. Phage display and kinetic selection of antibodies that specifically inhibit amyloid self-replication
  83. Selective targeting of primary and secondary nucleation pathways in Aβ42 aggregation using a rational antibody scanning method
  84. Corrigendum: Structural basis of synaptic vesicle assembly promoted by α-synuclein
  85. Structural Characterization of the Early Events in the Nucleation–Condensation Mechanism in a Protein Folding Process
  86. The RNF168 paralog RNF169 defines a new class of ubiquitylated histone reader involved in the response to DNA damage
  87. Emergence and evolution of an interaction between intrinsically disordered proteins
  88. Spinal motor neuron protein supersaturation patterns are associated with inclusion body formation in ALS
  89. MOAG-4 promotes the aggregation of α-synuclein by competing with self-protective electrostatic interactions
  90. Simultaneous quantification of protein order and disorder
  91. Bayesian weighing of electron cryo-microscopy data for integrative structural modeling
  92. Identification of an RNA Polymerase III Regulator Linked to Disease-Associated Protein Aggregation
  93. Inhibition of α-Synuclein Fibril Elongation by Hsp70 Is Governed by a Kinetic Binding Competition between α-Synuclein Species
  94. Widespread Proteome Remodeling and Aggregation in Aging C. elegans
  95. Networks of Dynamic Allostery Regulate Enzyme Function
  96. Principles of protein structural ensemble determination
  97. A natural product inhibits the initiation of α-synuclein aggregation and suppresses its toxicity
  98. Scaling behaviour and rate-determining steps in filamentous self-assembly
  99. Simultaneous NMR characterisation of multiple minima in the free energy landscape of an RNA UUCG tetraloop
  100. Systematic development of small molecules to inhibit specific microscopic steps of Aβ42 aggregation in Alzheimer’s disease
  101. β-Synuclein suppresses both the initiation and amplification steps of α-synuclein aggregation via competitive binding to surfaces
  102. Simultaneous Production of Amyloglucosidase and Exo-Polygalacturonase by Aspergillus niger in a Rotating Drum Reactor
  103. Structural basis of synaptic vesicle assembly promoted by α-synuclein
  104. Mutations associated with familial Parkinson’s disease alter the initiation and amplification steps of α-synuclein aggregation
  105. Metadynamic metainference: Enhanced sampling of the metainference ensemble using metadynamics
  106. A protein homeostasis signature in healthy brains recapitulates tissue vulnerability to Alzheimers disease
  107. Towards a structural biology of the hydrophobic effect in protein folding
  108. Chemical properties of lipids strongly affect the kinetics of the membrane-induced aggregation of α-synuclein
  109. Structure of a low-population binding intermediate in protein-RNA recognition
  110. Structural Ensembles of Membrane-bound α-Synuclein Reveal the Molecular Determinants of Synaptic Vesicle Affinity
  111. Structural Effects of Two Camelid Nanobodies Directed to Distinct C-Terminal Epitopes on α-Synuclein
  112. Rational design of mutations that change the aggregation rate of a protein while maintaining its native structure and stability
  113. Structural characterization of the interaction of α-synuclein nascent chains with the ribosomal surface and trigger factor
  114. A transcriptional signature of Alzheimer’s disease is associated with a metastable subproteome at risk for aggregation
  115. Kinetic analysis reveals the diversity of microscopic mechanisms through which molecular chaperones suppress amyloid formation
  116. Identification and Structural Characterization of an Intermediate in the Folding of the Measles Virus X Domain
  117. A structural ensemble of a ribosome–nascent chain complex during cotranslational protein folding
  118. A Fragment-Based Method of Creating Small-Molecule Libraries to Target the Aggregation of Intrinsically Disordered Proteins
  119. Molecular Recognition by Templated Folding of an Intrinsically Disordered Protein
  120. An anticancer drug suppresses the primary nucleation reaction that initiates the production of the toxic A 42 aggregates linked with Alzheimers disease
  121. Microfluidic Diffusion Analysis of the Sizes and Interactions of Proteins under Native Solution Conditions
  122. Metainference: A Bayesian inference method for heterogeneous systems
  123. Hamiltonian Dynamics of Protein Filament Formation
  124. Molecular mechanisms of protein aggregation from global fitting of kinetic models
  125. Particle-Based Monte-Carlo Simulations of Steady-State Mass Transport at Intermediate Péclet Numbers
  126. Structural Insights into the Calcium-Mediated Allosteric Transition in the C-Terminal Domain of Calmodulin from Nuclear Magnetic Resonance Measurements
  127. Using Pseudocontact Shifts and Residual Dipolar Couplings as Exact NMR Restraints for the Determination of Protein Structural Ensembles
  128. Parmbsc1: a refined force field for DNA simulations
  129. Structure-Free Validation of Residual Dipolar Coupling and Paramagnetic Relaxation Enhancement Measurements of Disordered Proteins
  130. ALS/FTD Mutation-Induced Phase Transition of FUS Liquid Droplets and Reversible Hydrogels into Irreversible Hydrogels Impairs RNP Granule Function
  131. Mapping the Protein Fold Universe Using the CamTube Force Field in Molecular Dynamics Simulations
  132. The inverted free energy landscape of an intrinsically disordered peptide by simulations and experiments
  133. Identification of Small Molecule Inhibitors of Tau Aggregation by Targeting Monomeric Tau As a Potential Therapeutic Approach for Tauopathies
  134. Latent analysis of unmodified biomolecules and their complexes in solution with attomole detection sensitivity
  135. Targeting disordered proteins with small molecules using entropy
  136. Chromatin Unfolding by Epigenetic Modifications Explained by Dramatic Impairment of Internucleosome Interactions: A Multiscale Computational Study
  137. A Rational Design Strategy for the Selective Activity Enhancement of a Molecular Chaperone toward a Target Substrate
  138. Rational design of antibodies targeting specific epitopes within intrinsically disordered proteins
  139. Probing the Residual Structure of the Low Populated Denatured State of ADA2h under Folding Conditions by Relaxation Dispersion Nuclear Magnetic Resonance Spectroscopy
  140. Reply to “Comment on ‘A Tensor-Free Method for the Structural and Dynamic Refinement of Proteins using Residual Dipolar Couplings’”
  141. Dynamic binding mode of a Synaptotagmin-1–SNARE complex in solution
  142. Analysis of the performance of the CHESHIRE and YAPP methods at CASD-NMR round 3
  143. Structure and Dynamics of GeoCyp: A Thermophilic Cyclophilin with a Novel Substrate Binding Mechanism That Functions Efficiently at Low Temperatures
  144. Widespread Proteome Remodeling and Aggregation in Aging C. elegans
  145. Structure and Dynamics of the Integrin LFA-1 I-Domain in the Inactive State Underlie its Inside-Out/Outside-In Signaling and Allosteric Mechanisms
  146. The physical basis of protein misfolding disorders
  147. A molecular chaperone breaks the catalytic cycle that generates toxic Aβ oligomers
  148. Lipid vesicles trigger α-synuclein aggregation by stimulating primary nucleation
  149. The s2D Method: Simultaneous Sequence-Based Prediction of the Statistical Populations of Ordered and Disordered Regions in Proteins
  150. Supersaturation is a major driving force for protein aggregation in neurodegenerative diseases
  151. A Tensor-Free Method for the Structural and Dynamical Refinement of Proteins using Residual Dipolar Couplings
  152. Structure of a low-population intermediate state in the release of an enzyme product
  153. The CamSol Method of Rational Design of Protein Mutants with Enhanced Solubility
  154. Analysis of the hierarchical structure of the B. subtilis transcriptional regulatory network
  155. The Computational Studies of Co-Translational Protein Folding
  156. Biophysical approaches for the study of interactions between molecular chaperones and protein aggregates
  157. Druggability of Intrinsically Disordered Proteins
  158. Structure and Dynamics of Intrinsically Disordered Proteins
  159. The H50Q Mutation Induces a 10-fold Decrease in the Solubility of α-Synuclein
  160. Characterization of the Conformational Fluctuations in the Josephin Domain of Ataxin-3
  161. A Relationship between the Transient Structure in the Monomeric State and the Aggregation Propensities of α-Synuclein and β-Synuclein
  162. ADP ribosylation adapts an ER chaperone response to short-term fluctuations in unfolded protein load
  163. Understanding the frustration arising from the competition between function, misfolding, and aggregation in a globular protein
  164. Identification and characterization of PKCγ, a kinase associated with SCA14, as an amyloidogenic protein
  165. NMR characterization of the conformational fluctuations of the human lymphocyte function‐associated antigen‐1 I‐domain
  166. Equilibrium simulations of proteins using molecular fragment replacement and NMR chemical shifts
  167. Archaeal MBF1 binds to 30S and 70S ribosomes via its helix–turn–helix domain
  168. Cyclophilin A catalyzes proline isomerization by an electrostatic handle mechanism
  169. Statistical Mechanics of the Denatured State of a Protein Using Replica-Averaged Metadynamics
  170. A tensor-free method for the structural and dynamical refinement of proteins using residual dipolar couplings
  171. Flexible anchoring of archaeal MBF1 on ribosomes suggests role as recruitment factor
  172. Erratum: The amyloid state and its association with protein misfolding diseases
  173. Direct observation of the three regions in α-synuclein that determine its membrane-bound behaviour
  174. The amyloid state and its association with protein misfolding diseases
  175. Understanding the Influence of Codon Translation Rates on Cotranslational Protein Folding
  176. Solution conditions determine the relative importance of nucleation and growth processes in α-synuclein aggregation
  177. Determination of the Individual Roles of the Linker Residues in the Interdomain Motions of Calmodulin Using NMR Chemical Shifts
  178. ALMOST: An all atom molecular simulation toolkit for protein structure determination
  179. Spatial Propagation of Protein Polymerization
  180. Chemical kinetics for drug discovery to combat protein aggregation diseases
  181. Targeting the Intrinsically Disordered Structural Ensemble of α-Synuclein by Small Molecules as a Potential Therapeutic Strategy for Parkinson’s Disease
  182. The dynamics of interleukin‐8 and its interaction with human CXC receptor I peptide
  183. A Conformational Ensemble Derived Using NMR Methyl Chemical Shifts Reveals a Mechanical Clamping Transition That Gates the Binding of the HU Protein to DNA
  184. New opportunities for tensor-free calculations of residual dipolar couplings for the study of protein dynamics
  185. A Simple Lattice Model That Captures Protein Folding, Aggregation and Amyloid Formation
  186. Kinetic modelling indicates that fast-translating codons can coordinate cotranslational protein folding by avoiding misfolded intermediates
  187. Structure of a Misfolded Intermediate of a PDZ Domain
  188. Higher Order Amyloid Fibril Structure by MAS NMR and DNP Spectroscopy
  189. A Clear View of Polymorphism, Twist, and Chirality in Amyloid Fibril Formation
  190. Replica-Averaged Metadynamics
  191. Widespread Aggregation and Neurodegenerative Diseases Are Associated with Supersaturated Proteins
  192. pE-DB: a database of structural ensembles of intrinsically disordered and of unfolded proteins
  193. Erratum: “Molecular dynamics simulations with replica-averaged structural restraints generate structural ensembles according to the maximum entropy principle” [J. Chem. Phys. 138, 094112 (2013)]
  194. Subdomain Architecture and Stability of a Giant Repeat Protein
  195. Cucurbit[8]uril and Blue-Box: High-Energy Water Release Overwhelms Electrostatic Interactions
  196. A Relationship between the Aggregation Rates of α-Synuclein Variants and the β-Sheet Populations in Their Monomeric Forms
  197. Characterization of the Interdomain Motions in Hen Lysozyme Using Residual Dipolar Couplings as Replica-Averaged Structural Restraints in Molecular Dynamics Simulations
  198. Structures of the Excited States of Phospholamban and Shifts in Their Populations upon Phosphorylation
  199. In-Cell NMR Characterization of the Secondary Structure Populations of a Disordered Conformation of α-Synuclein within E. coli Cells
  200. A geometrical parametrization of C1′-C5′ RNA ribose chemical shifts calculated by density functional theory
  201. Identification of small-molecule binding pockets in the soluble monomeric form of the Aβ42 peptide
  202. Nanobodies Raised against Monomeric α-Synuclein Distinguish between Fibrils at Different Maturation Stages
  203. Single-Molecule Measurements of Transient Biomolecular Complexes through Microfluidic Dilution
  204. A method of determining RNA conformational ensembles using structure-based calculations of residual dipolar couplings
  205. Proliferation of amyloid-β42 aggregates occurs through a secondary nucleation mechanism
  206. Integration and characterization of solid wall electrodes in microfluidic devices fabricated in a single photolithography step
  207. The codon information index: a quantitative measure of the information provided by the codon bias
  208. Characterization of the free-energy landscapes of proteins by NMR-guided metadynamics
  209. Atomic structure and hierarchical assembly of a cross-β amyloid fibril
  210. Protein self-assembly intermediates
  211. Molecular dynamics simulations with replica-averaged structural restraints generate structural ensembles according to the maximum entropy principle
  212. Erratum: Prediction of variable translation rate effects on cotranslational protein folding
  213. Analysis of the Contributions of Ring Current and Electric Field Effects to the Chemical Shifts of RNA Bases
  214. Assessment of the Use of NMR Chemical Shifts as Replica-Averaged Structural Restraints in Molecular Dynamics Simulations to Characterize the Dynamics of Proteins
  215. R state structure of monomeric phospholamban (C36A, C41F, C46A)
  216. Sequence-Based Prediction of Protein Behavior
  217. The Kinetics and Mechanisms of Amyloid Formation
  218. Characterization of Free Energy Landscapes of Proteins using NMR Spectroscopy
  219. In Vivo Translation Rates Can Substantially Delay the Co-Translational Folding of the E. Coli Cytosolic Proteome
  220. Thermodynamics of an Intrinsically Disordered Protein by Atomistic Simulations
  221. In vivo translation rates can substantially delay the cotranslational folding of the Escherichia coli cytosolic proteome
  222. A Rationally Designed Six-Residue Swap Generates Comparability in the Aggregation Behavior of α-Synuclein and β-Synuclein
  223. Twisting Transition between Crystalline and Fibrillar Phases of Aggregated Peptides
  224. In support of the BMRB
  225. ADP ribosylation adapts an ER chaperone response to short-term fluctuations in unfolded protein load
  226. From Macroscopic Measurements to Microscopic Mechanisms of Protein Aggregation
  227. Sequence-Based Prediction of Protein Solubility
  228. Trigger Factor Slows Co-translational Folding through Kinetic Trapping while Sterically Protecting the Nascent Chain from Aberrant Cytosolic Interactions
  229. Determination of structural fluctuations of proteins from structure-based calculations of residual dipolar couplings
  230. Protein Structure Validation Using Side-Chain Chemical Shifts
  231. Structure of an Intermediate State in Protein Folding and Aggregation
  232. Proteome folding and aggregation
  233. Fibrillogenic propensity of the GroEL apical domain: A Janus-faced minichaperone
  234. Determination of Secondary Structure Populations in Disordered States of Proteins Using Nuclear Magnetic Resonance Chemical Shifts
  235. Characterization of the Conformational Equilibrium between the Two Major Substates of RNase A Using NMR Chemical Shifts
  236. Blind Testing of Routine, Fully Automated Determination of Protein Structures from NMR Data
  237. Prediction of variable translation rate effects on cotranslational protein folding
  238. Determination of Conformational Equilibria in Proteins Using Residual Dipolar Couplings
  239. Experimental free energy surfaces reveal the mechanisms of maintenance of protein solubility
  240. Coarse-grained model for protein folding based on structural profiles
  241. Inversion of the Balance between Hydrophobic and Hydrogen Bonding Interactions in Protein Folding and Aggregation
  242. ALS mutations in FUS cause neuronal dysfunction and death in Caenorhabditis elegans by a dominant gain-of-function mechanism
  243. Metastability of Native Proteins and the Phenomenon of Amyloid Formation
  244. Nucleated Polymerisation in the Presence of Pre-Formed Seed Filaments
  245. Using Side-Chain Aromatic Proton Chemical Shifts for a Quantitative Analysis of Protein Structures
  246. Using Side-Chain Aromatic Proton Chemical Shifts for a Quantitative Analysis of Protein Structures
  247. Excited-State Control of Protein Activity
  248. The A53T Mutation is Key in Defining the Differences in the Aggregation Kinetics of Human and Mouse α-Synuclein
  249. Nucleated polymerization with secondary pathways. II. Determination of self-consistent solutions to growth processes described by non-linear master equations
  250. Nucleated polymerization with secondary pathways. I. Time evolution of the principal moments
  251. Nucleated polymerization with secondary pathways. III. Equilibrium behavior and oligomer populations
  252. Protein Solubility and Protein Homeostasis: A Generic View of Protein Misfolding Disorders
  253. Using Chemical Shifts to Determine Structural Changes in Proteins upon Complex Formation
  254. Structure-based prediction of methyl chemical shifts in proteins
  255. The statistical theory of allostery
  256. 1H, 13C and 15N resonance assignments of human muscle acylphosphatase
  257. Asymmetric folding pathways and transient misfolding in a coarse-grained model of proteins
  258. Effects of the Known Pathogenic Mutations on the Aggregation Pathway of the Amyloidogenic Peptide of Apolipoprotein A-I
  259. Detection of early locomotor abnormalities in a Drosophila model of Alzheimer's disease
  260. Faculty Opinions recommendation of A transient and low-populated protein-folding intermediate at atomic resolution.
  261. On the Effect of the Ribosome and Trigger Factor on Nascent Chain Protein Folding
  262. New Scenarios of Protein Folding Can Occur on the Ribosome
  263. The iFly tracking system for an automated locomotor and behavioural analysis of Drosophila melanogaster
  264. Interactions in the native state of monellin, which play a protective role against aggregation
  265. Protein Dynamics: Moore's Law in Molecular Biology
  266. Amyloid-like Aggregates Sequester Numerous Metastable Proteins with Essential Cellular Functions
  267. Transient Tertiary Structure Formation within the Ribosome Exit Port
  268. Focus on Physical Principles of Protein Behavior in the Cell
  269. Structural characterization of a misfolded intermediate populated during the folding process of a PDZ domain
  270. Translationally optimal codons associate with aggregation-prone sites in proteins
  271. Accurate Determination of Interstrand Distances and Alignment in Amyloid Fibrils by Magic Angle Spinning NMR
  272. Proteome-Level Interplay between Folding and Aggregation Propensities of Proteins
  273. Enzymatic activity in disordered states of proteins
  274. Functional interactions as a survival strategy against abnormal aggregation
  275. Faculty Opinions recommendation of Widespread protein aggregation as an inherent part of aging in C. elegans.
  276. Using NMR Chemical Shifts as Structural Restraints in Molecular Dynamics Simulations of Proteins
  277. Physicochemical Determinants of Chaperone Requirements
  278. Time Averaging of NMR Chemical Shifts in the MLF Peptide in the Solid State
  279. Intrinsic Determinants of Neurotoxic Aggregate Formation by the Amyloid β Peptide
  280. Faculty Opinions recommendation of NMR spectroscopy brings invisible protein states into focus.
  281. Efficient identification of near-native conformations in ab initio protein structure prediction using structural profiles
  282. Derivation of a solubility condition for proteins from an analysis of the competition between folding and aggregation
  283. Determination of the Free Energy Landscape of α-Synuclein Using Spin Label Nuclear Magnetic Resonance Measurements
  284. An Analytical Solution to the Kinetics of Breakable Filament Assembly
  285. Accurate Random Coil Chemical Shifts from an Analysis of Loop Regions in Native States of Proteins
  286. Analysis of Sub-τc and Supra-τc Motions in Protein Gβ1 Using Molecular Dynamics Simulations
  287. Fast and Accurate Predictions of Protein NMR Chemical Shifts from Interatomic Distances
  288. On the Mechanism of Nonspecific Inhibitors of Protein Aggregation: Dissecting the Interactions of α-Synuclein with Congo Red and Lacmoid
  289. A Condensation-Ordering Mechanism in Nanoparticle-Catalyzed Peptide Aggregation
  290. Factors That Affect the Degree of Twist in β-Sheet Structures: A Molecular Dynamics Simulation Study of a Cross-β Filament of the GNNQQNY Peptide
  291. Physicochemical principles that regulate the competition between functional and dysfunctional association of proteins
  292. Physical Principles of Protein Behavior in the Cell
  293. Folding of Small Proteins by Monte Carlo Simulations with Chemical Shift Restraints without the Use of Molecular Fragment Replacement or Structural Homology
  294. Competition between Intramolecular and Intermolecular Interactions in an Amyloid-Forming Protein
  295. Position-Dependent Electrostatic Protection against Protein Aggregation
  296. A Relationship between mRNA Expression Levels and Protein Solubility in E. coli
  297. Mutational Analysis of the Aggregation-Prone and Disaggregation-Prone Regions of Acylphosphatase
  298. Toward an Accurate Determination of Free Energy Landscapes in Solution States of Proteins
  299. The mechanism of folding of Im7 reveals competition between functional and kinetic evolutionary constraints
  300. Factors That Affect the Degree of Twist in β-Sheet Structures: A Molecular Dynamics Simulation Study of a Cross-β Filament of the GNNQQNY Peptide
  301. Competition between Folding, Native-State Dimerisation and Amyloid Aggregation in β-Lactoglobulin
  302. Correlation between mRNA expression levels and protein aggregation propensities in subcellular localisations
  303. Quantitative approaches to defining normal and aberrant protein homeostasis
  304. Networks in Cell Biology
  305. Self-Templated Nucleation in Peptide and Protein Aggregation
  306. Comparison of successive transition states for folding reveals alternative early folding pathways of two homologous proteins
  307. Determination of Protein Structures in the Solid State from NMR Chemical Shifts
  308. Structure Determination of Protein−Protein Complexes Using NMR Chemical Shifts: Case of an Endonuclease Colicin−Immunity Protein Complex
  309. A Generic Mechanism of Emergence of Amyloid Protofilaments from Disordered Oligomeric Aggregates
  310. Inhibition of α-Synuclein Fibrillization by Dopamine Is Mediated by Interactions with Five C-Terminal Residues and with E83 in the NAC Region
  311. Introduction to the special issue of GENE
  312. A stochastic method for the reconstruction of protein structures from one-dimensional structural profiles
  313. Competition between protein aggregation and protein complex formation
  314. Structure and Dynamics of a Partially Folded Protein Are Decoupled from Its Mechanism of Aggregation
  315. ChemInform Abstract: The Zyggregator Method for Predicting Protein Aggregation Propensities
  316. Protein dynamics under light control
  317. Characterizing the First Steps of Amyloid Formation for the ccβ Peptide
  318. Prediction by Graph Theoretic Measures of Structural Effects in Proteins Arising from Non-Synonymous Single Nucleotide Polymorphisms
  319. Prediction of Aggregation-Prone Regions in Structured Proteins
  320. Mapping of Two Networks of Residues That Exhibit Structural and Dynamical Changes upon Binding in a PDZ Domain Protein
  321. Biological function in a non-native partially folded state of a protein
  322. A Coupled Equilibrium Shift Mechanism in Calmodulin-Mediated Signal Transduction
  323. Molecular determinants of the aggregation behavior of α- and β-synuclein
  324. Determination of the Transition State Ensemble for the Folding of Ubiquitin from a Combination of Φ and Ψ Analyses
  325. Characterisation of transition state structures for protein folding using 'high', 'medium' and 'low'  -values
  326. Towards quantitative predictions in cell biology using chemical properties of proteins
  327. The Zyggregator method for predicting protein aggregation propensities
  328. Stochastic reconstruction of protein structures from effective connectivity profiles
  329. Calculation of the free energy barriers in the oligomerisation of Ab
  330. Role of Intermolecular Forces in Defining Material Properties of Protein Nanofibrils
  331. The Distribution of Residues in a Polypeptide Sequence Is a Determinant of Aggregation Optimized by Evolution
  332. Influence of the fluctuations of the alignment tensor on the analysis of the structure and dynamics of proteins using residual dipolar couplings
  333. Systematic In Vivo Analysis of the Intrinsic Determinants of Amyloid β Pathogenicity
  334. Importance of Metastable States in the Free Energy Landscapes of Polypeptide Chains
  335. More charges against aggregation
  336. Characterisation of Amyloid Fibril Formation by Small Heat-shock Chaperone Proteins Human αA-, αB- and R120G αB-Crystallins
  337. Molecular dynamics simulations from putative transition states of α-spectrin SH3 domain
  338. Characterization of the nucleation barriers for protein aggregation and amyloid formation
  339. Protein structure determination from NMR chemical shifts
  340. Similarities in the thermodynamics and kinetics of aggregation of disease-related Aβ(1-40) peptides
  341. Life on the edge: a link between gene expression levels and aggregation rates of human proteins
  342. Determination of conformationally heterogeneous states of proteins
  343. Prediction of Local Structural Stabilities of Proteins from Their Amino Acid Sequences
  344. The MUMO (minimal under-restraining minimal over-restraining) method for the determination of native state ensembles of proteins
  345. A PDZ domain recapitulates a unifying mechanism for protein folding
  346. The Structurally Constrained Neutral Model of Protein Evolution
  347. Structural Reorganisation and Potential Toxicity of Oligomeric Species Formed during the Assembly of Amyloid Fibrils
  348. BPPred: A Web-based computational tool for predicting biophysical parameters of proteins
  349. Geometry, Energetics, and Dynamics of Hydrogen Bonds in Proteins:  Structural Information Derived from NMR Scalar Couplings
  350. STRUCTURAL BIOLOGY: Dynamic Visions of Enzymatic Reactions
  351. Characterization of the residual structure in the unfolded state of the Δ131Δ fragment of staphylococcal nuclease
  352. Relation between native ensembles and experimental structures of proteins
  353. Structural Comparison of the Two Alternative Transition States for Folding of TI I27
  354. Theoretical Approaches to Protein Aggregation
  355. Structural Interpretation of Hydrogen Exchange Protection Factors in Proteins: Characterization of the Native State Fluctuations of CI2
  356. Determination of an ensemble of structures representing the intermediate state of the bacterial immunity protein Im7
  357. Effective interactions between chaotropic agents and proteins
  358. Transition State Contact Orders Correlate with Protein Folding Rates
  359. Form of Growing Strings
  360. Determination of the folding transition states of barnase by using Φ I -value-restrained simulations validated by double mutant Φ IJ -values
  361. Interpreting Dynamically-Averaged Scalar Couplings in Proteins
  362. Prediction of “Aggregation-prone” and “Aggregation-susceptible” Regions in Proteins Associated with Neurodegenerative Diseases
  363. Comparison of Sequence-Based and Structure-Based Energy Functions for the Reversible Folding of a Peptide
  364. Detection of non-native hydrophobic interactions in the denatured state of lysozyme by molecular dynamics simulations
  365. A glimpse at the organization of the protein universe
  366. Formation of Native and Non-native Interactions in Ensembles of Denatured ACBP Molecules from Paramagnetic Relaxation Enhancement Studies
  367. Looking at structure, stability, and evolution of proteins through the principal eigenvector of contact matrices and hydrophobicity profiles
  368. Towards complete descriptions of the free–energy landscapes of proteins
  369. Simultaneous determination of protein structure and dynamics
  370. Protein folding and the organization of the protein topology universe
  371. Mapping Long-Range Interactions in α-Synuclein using Spin-Label NMR and Ensemble Molecular Dynamics Simulations
  372. Prediction of Site-Specific Amino Acid Distributions and Limits of Divergent Evolutionary Changes in Protein Sequences
  373. Principal eigenvector of contact matrices and hydrophobicity profiles in proteins
  374. Comparison of the Transition States for Folding of Two Ig-like Proteins from Different Superfamilies
  375. Prediction of the Absolute Aggregation Rates of Amyloidogenic Polypeptide Chains
  376. Low-populated folding intermediates of Fyn SH3 characterized by relaxation dispersion NMR
  377. Molecular Dynamics Studies of the Process of Amyloid Aggregation of Peptide Fragments of Transthyretin
  378. Determination of Protein Structures Consistent with NMR Order Parameters
  379. Reconstruction of Protein Structures from a Vectorial Representation
  380. Transition states for protein folding have native topologies despite high structural variability
  381. Determination of an Ensemble of Structures Representing the Denatured State of the Bovine Acyl-Coenzyme A Binding Protein
  382. Inhibition of protein crystallization by evolutionary negative design
  383. Comparison of the transition state ensembles for folding of Im7 and Im9 determined using all-atom molecular dynamics simulations with ϕ value restraints
  384. Rare Fluctuations of Native Proteins Sampled by Equilibrium Hydrogen Exchange
  385. Structures and relative free energies of partially folded states of proteins
  386. Statistical Properties of Neutral Evolution
  387. Calculation of Mutational Free Energy Changes in Transition States for Protein Folding
  388. Analysis of the distributed computing approach applied to the folding of a small β peptide
  389. Protein folding and misfolding: a paradigm of self–assembly and regulation in complex biological systems
  390. Connectivity of Neutral Networks, Overdispersion, and Structural Conservation in Protein Evolution
  391. Protein folding: bringing theory and experiment closer together
  392. Self-consistent determination of the transition state for protein folding: Application to a fibronectin type III domain
  393. Validity of Gō Models: Comparison with a Solvent-Shielded Empirical Energy Decomposition
  394. Determination of the structures of distinct transition state ensembles for a β-sheet peptide with parallel folding pathways
  395. Determination of a Transition State at Atomic Resolution from Protein Engineering Data
  396. Lack of Self-Averaging in Neutral Evolution of Proteins
  397. Small-world view of the amino acids that play a key role in protein folding
  398. Native and non-native interactions along protein folding and unfolding pathways
  399. Statistical properties of contact vectors
  400. Automated assignment of SCOP and CATH protein structure classifications from FSSP scores
  401. Energetics of enzyme stability
  402. Three key residues form a critical contact network in a protein folding transition state
  403. How to guarantee optimal stability for most representative structures in the protein data bank
  404. Comparison of two optimization methods to derive energy parameters for protein folding: Perceptron and Z score
  405. Toward an energy function for the contact map representation of proteins
  406. Toward an energy function for the contact map representation of proteins
  407. Structurally constrained protein evolution: results from a lattice simulation
  408. A statistical mechanical method to optimize energy functions for protein folding
  409. Can a pairwise contact potential stabilize native protein folds against decoys obtained by threading?
  410. Protein folding using contact maps
  411. Comparison of two optimization methods to derive energy parameters for protein folding: Perceptron andZ score
  412. Folding Lennard-Jones proteins by a contact potential
  413. Neutral Evolution of Model Proteins: Diffusion in Sequence Space and Overdispersion
  414. Hydrophobicity and unique folding of selected polymers
  415. Protein Folding in Contact Map Space
  416. Statistical properties of contact maps
  417. An optimal derivation of a potential for protein folding
  418. Pairwise contact potentials are unsuitable for protein folding
  419. Efficient dynamics in the space of contact maps
  420. High-Dimensional Bak-Sneppen Model
  421. Protein stability and foldability–designability complementarity
  422. Recovery of protein structure from contact maps
  423. Stability Threshold as a Selection Principle for Protein Design
  424. Growth with memory
  425. Modified configurational bias Monte Carlo method for simulation of polymer systems
  426. Model of correlated evolution
  427. Hot sandpiles
  428. Optimal Protein Design Procedure
  429. Diffusion in disordered media as a process with memory
  430. Disordered flat phase and phase diagram for restricted solid-on-solid models of fcc (110) surfaces
  431. Quenched disorder, memory, and self-organization
  432. Evolution of the missing row deconstruction on Rh (110)
  433. A mean-field study of the temperature dependence of the layer magnetizations in a semi-infinite ising model
  434. Magnetic-Phase Transitions of Ising Surfaces with Modified Surface-Bulk Coupling: a Monte Carlo Study
  435. Network views of the cell
  436. Introduction
  437. Protein folding using inter-residue contact