All Stories

  1. Chaperone-mediated MHC-I peptide exchange in antigen presentation
  2. Experimental Structures of Antibody/MHC-I Complexes Reveal Details of Epitopes Overlooked by Computational Prediction
  3. Experimental structures of antibody/MHC-I complexes reveal details of epitopes overlooked by computational prediction
  4. SARS-CoV-2 antibodies recognize 23 distinct epitopic sites on the receptor binding domain
  5. Chaperone function in antigen presentation by MHC class I molecules—tapasin in the PLC and TAPBPR beyond
  6. SARS-CoV-2 antibodies recognize 23 distinct epitopic sites on the receptor binding domain
  7. Structural mechanism of tapasin-mediated MHC-I peptide loading in antigen presentation
  8. Chaperones and Catalysts: How Antigen Presentation Pathways Cope With Biological Necessity
  9. Mucus sialylation determines intestinal host-commensal homeostasis
  10. Structures of synthetic nanobody–SARS-CoV-2 receptor-binding domain complexes reveal distinct sites of interaction
  11. Structures of synthetic nanobody–SARS-CoV-2–RBD complexes reveal distinct sites of interaction and recognition of variants
  12. Structural mechanism of DNA recognition by the p204 HIN domain
  13. Synthetic nanobody–SARS-CoV-2 receptor-binding domain structures identify distinct epitopes
  14. Structural and dynamic studies of TAPBPR and Tapasin reveal the mechanism of peptide loading of MHC-I molecules
  15. Structure determination of the CAMP factor ofStreptococcus agalactiaewith the aid of an MBP tag and insights into membrane-surface attachment
  16. MHC‐restricted Ag85B‐specific CD8+ T cells are enhanced by recombinant BCG prime and DNA boost immunization in mice
  17. Structural aspects of chaperone-mediated peptide loading in the MHC-I antigen presentation pathway
  18. MHC Molecules, T cell Receptors, Natural Killer Cell Receptors, and Viral Immunoevasins—Key Elements of Adaptive and Innate Immunity
  19. Structure and Function of Molecular Chaperones that Govern Immune Peptide Loading
  20. Revisit of Reconstituted 30-nm Nucleosome Arrays Reveals an Ensemble of Dynamic Structures
  21. The Role of Molecular Flexibility in Antigen Presentation and T Cell Receptor-Mediated Signaling
  22. Peptide exchange on MHC-I by TAPBPR is driven by a negative allostery release cycle
  23. Functional and structural characterization of zebrafish ASC
  24. Effects of Cross-Presentation, Antigen Processing, and Peptide Binding in HIV Evasion of T Cell Immunity
  25. Crystal structure of human NLRP12 PYD domain and implication in homotypic interaction
  26. Crystal structure of a TAPBPR–MHC I complex reveals the mechanism of peptide editing in antigen presentation
  27. An allosteric site in the T-cell receptor Cβ domain plays a critical signalling role
  28. Design of an expression system to enhance MBP-mediated crystallization
  29. Interaction of TAPBPR, a tapasin homolog, with MHC-I molecules promotes peptide editing
  30. Structural Mechanisms of Nucleosome Recognition by Linker Histones
  31. RAGE is a nucleic acid receptor that promotes inflammatory responses to DNA
  32. The Catalytic Subunit of the SWR1 Remodeler Is a Histone Chaperone for the H2A.Z-H2B Dimer
  33. Novel complex MAD phasing and RNase H structural insights using selenium oligonucleotides
  34. Crystal Structures of the Toll/Interleukin-1 Receptor (TIR) Domains from the Brucella Protein TcpB and Host Adaptor TIRAP Reveal Mechanisms of Molecular Mimicry
  35. RAGE is a nucleic acid receptor that promotes inflammatory responses to DNA
  36. RAGE is a nucleic acid receptor that promotes inflammatory responses to DNA
  37. Structure of the caspase-recruitment domain from a zebrafish guanylate-binding protein
  38. A Conserved Mechanism for Centromeric Nucleosome Recognition by Centromere Protein CENP-C
  39. Structure of the Absent in Melanoma 2 (AIM2) Pyrin Domain Provides Insights into the Mechanisms of AIM2 Autoinhibition and Inflammasome Assembly
  40. The structure of the CARD8 caspase-recruitment domain suggests its association with the FIIND domain and procaspases through adjacent surfaces
  41. Structure of the NLRP1 caspase recruitment domain suggests potential mechanisms for its association with procaspase‐1
  42. Molecular mechanisms for the subversion of MyD88 signaling by TcpC from virulent uropathogenic Escherichia coli
  43. Two Distinct Binding Modes Define the Interaction of Brox with the C-Terminal Tails of CHMP5 and CHMP4B
  44. Structures of the HIN Domain:DNA Complexes Reveal Ligand Binding and Activation Mechanisms of the AIM2 Inflammasome and IFI16 Receptor
  45. The Phe105 Loop of Alix Bro1 Domain Plays a Key Role in HIV-1 Release
  46. Synthesis and Crystallographic Analysis of 5-Se-Thymidine DNAs
  47. Derivatization of DNAs with selenium at 6-position of guanine for function and crystal structure studies
  48. 218 Mechanism of TOLL/IL-1 receptor domain dimerization and signaling revealed by a crystal structure of the MYD88
  49. Oxygen Replacement with Selenium at the Thymidine 4-Position for the Se Base Pairing and Crystal Structure Studies
  50. Synthesis of a 2‘-Se-thymidine Phosphoramidite and Its Incorporation into Oligonucleotides for Crystal Structure Study
  51. Selenium derivatization of nucleic acids for crystallography
  52. Crystal Structure of AqpZ Tetramer Reveals Two Distinct Arg-189 Conformations Associated with Water Permeation through the Narrowest Constriction of the Water-conducting Channel
  53. Protein Data Bank depositions from synchrotron sources
  54. Crystallization and preliminary crystallographic analysis of theEscherichia coliwater channel AqpZ
  55. Structural genomics: A pipeline for providing structures for the biologist
  56. AutoDep: a web-based system for deposition and validation of macromolecular structural information
  57. Deposition of structure factors at the Protein Data Bank
  58. Protein Data Bank (PDB): Database of Three-Dimensional Structural Information of Biological Macromolecules
  59. Crystallography & NMR System: A New Software Suite for Macromolecular Structure Determination
  60. Protein Hydration Observed by X-ray Diffraction