All Stories

  1. Adeno-Associated virus 8 delivers an immunomodulatory peptide to mouse liver more efficiently than to rat liver
  2. A bioengineered probiotic for the oral delivery of a peptide Kv1.3 channel blocker to treat rheumatoid arthritis
  3. A Conjugate between Lqh-8/6, a Natural Peptide Analogue of Chlorotoxin, and Doxorubicin Efficiently Induces Glioma Cell Death
  4. A bioengineered probiotic for the oral delivery of a peptide Kv1.3 channel blocker to treat rheumatoid arthritis
  5. Comprehensive engineering of the tarantula venom peptide huwentoxin-IV to inhibit the human voltage-gated sodium channel hNav1.7
  6. Comprehensive engineering of the tarantula venom peptide huwentoxin-IV to inhibit the human voltage-gated sodium channel hNav17
  7. The molecular evolution of feathers with direct evidence from fossils
  8. Synthesis, folding, structure and activity of a predicted peptide from the sea anemone Oulactis sp. with an ShKT fold
  9. Peptide therapeutics from venom: Current status and potential
  10. Structure, synthesis and potassium channel blocking activity of a new sea anemone peptide
  11. Identification and therapeutic modulation of a pro-inflammatory subset of disease-associated-microglia in Alzheimer’s disease
  12. Corrigendum to “Structure, folding and stability of a minimal homologue from Anemonia sulcata of the sea anemone potassium channel blocker ShK” [Peptides 99 (2018) 169–178]
  13. Targeting KCa1.1 Channels with a Scorpion Venom Peptide for the Therapy of Rat Models of Rheumatoid Arthritis
  14. Structure, folding and stability of a minimal homologue from Anemonia sulcata of the sea anemone potassium channel blocker ShK
  15. Enantioselective synthesis of Fmoc- -3-(2-benzothienyl)alanine (2-BtAla) via diastereoselective alkylation of a glycine equivalent
  16. Prolonged immunomodulation in inflammatory arthritis using the selective Kv1.3 channel blocker HsTX1[R14A] and its PEGylated analog
  17. A systems pharmacology-based approach to identify novel Kv1.3 channel-dependent mechanisms in microglial activation
  18. Distribution and kinetics of the Kv1.3-blocking peptide HsTX1[R14A] in experimental rats
  19. Reinvestigation of the biological activity of d-allo-ShK protein
  20. The Single Disulfide-Directed β-Hairpin Fold. Dynamics, Stability, and Engineering
  21. KCa1.1 channels regulate β 1 -integrin function and cell adhesion in rheumatoid arthritis fibroblast-like synoviocytes
  22. Insensitivity to pain induced by a potent selective closed-state Nav1.7 inhibitor
  23. Enabling Noninvasive Systemic Delivery of the Kv1.3-Blocking Peptide HsTX1[R14A] via the Buccal Mucosa
  24. Pulmonary Delivery of the Kv1.3-Blocking Peptide HsTX1[R14A] for the Treatment of Autoimmune Diseases
  25. N-terminally extended analogues of the K+channel toxin fromStichodactyla helianthusas potent and selective blockers of the voltage-gated potassium channel Kv1.3
  26. Buccal mucosal delivery of a potent peptide leads to therapeutically-relevant plasma concentrations for the treatment of autoimmune diseases
  27. Development of Highly Selective Kv1.3-Blocking Peptides Based on the Sea Anemone Peptide ShK
  28. FITC-Conjugated Cyclic RGD Peptides as Fluorescent Probes for Staining Integrin αvβ3/αvβ5 in Tumor Tissues
  29. Kv1.3 channel-blocking immunomodulatory peptides from parasitic worms: implications for autoimmune diseases
  30. A potent and Kv1.3-selective analogue of the scorpion toxin HsTX1 as a potential therapeutic for autoimmune diseases
  31. Blocking KV1.3 Channels Inhibits Th2 Lymphocyte Function and Treats a Rat Model of Asthma
  32. Total Synthesis of Human Hepcidin through Regioselective Disulfide-Bond Formation by using the Safety-Catch Cysteine Protecting Group 4,4′-Dimethylsulfinylbenzhydryl
  33. Blockade of Kv1.3 channels ameliorates radiation-induced brain injury
  34. A Potent and Selective Peptide Blocker of the Kv1.3 Channel: Prediction from Free-Energy Simulations and Experimental Confirmation
  35. Blocking KCa3.1 Channels Increases Tumor Cell Killing by a Subpopulation of Human Natural Killer Lymphocytes
  36. 99mTc-Galacto-RGD2: A Novel 99mTc-Labeled Cyclic RGD Peptide Dimer Useful for Tumor Imaging
  37. A C-terminally amidated analogue of ShK is a potent and selective blocker of the voltage-gated potassium channel Kv1.3
  38. Expression and isotopic labelling of the potassium channel blocker ShK toxin as a thioredoxin fusion protein in bacteria
  39. Durable Pharmacological Responses from the Peptide ShK-186, a Specific Kv1.3 Channel Inhibitor That Suppresses T Cell Mediators of Autoimmune Disease
  40. Development of a sea anemone toxin as an immunomodulator for therapy of autoimmune diseases
  41. Analogs of the Sea Anemone Potassium Channel Blocker ShK for the Treatment of Autoimmune Diseases
  42. Potassium Channel Modulation by a Toxin Domain in Matrix Metalloprotease 23
  43. Kv1.3 potassium channels as a therapeutic target in multiple sclerosis
  44. Chemical synthesis and characterization of ShK toxin: a potent potassium channel inhibitor from a sea anemone
  45. Synthesis of the cardiac inotropic polypeptide anthopleurin-A
  46. Chemical synthesis of a neurotoxic polypeptide from the sea anemone Stichodactyla helianthus+
  47. Engineering a Stable and Selective Peptide Blocker of the Kv1.3 Channel in T Lymphocytes
  48. Efficient Synthesis of Protected L-Phosphonophenylalanine (Ppa) Derivatives Suitable for Solid Phase Synthesis
  49. Imaging of Effector Memory T Cells during a Delayed-Type Hypersensitivity Reaction and Suppression by Kv1.3 Channel Block
  50. The D-Diastereomer of ShK Toxin Selectively Blocks Voltage-gated K+Channels and Inhibits T Lymphocyte Proliferation
  51. Characterization of the Functional Properties of the Voltage-Gated Potassium Channel Kv1.3 in Human CD4+ T Lymphocytes
  52. Efficient synthesis of protected l-phosphonophenylalanine (Ppa) derivatives suitable for solid phase peptide synthesis
  53. Targeted tyrosine iodination in a multi-tyrosine vasopressin analog
  54. Kv1.3 channels are a therapeutic target for T cell-mediated autoimmune diseases
  55. Potassium channels Kv1.3 and Kv1.5 are expressed on blood-derived dendritic cells in the central nervous system
  56. A short practical synthesis of 2′-deoxymugineic acid
  57. Targeting Effector Memory T Cells with a Selective Peptide Inhibitor of Kv1.3 Channels for Therapy of Autoimmune Diseases
  58. Potassium Channel Blockade by the Sea Anemone Toxin ShK for the Treatment of Multiple Sclerosis and Other Autoimmune Diseases
  59. Bass Hepcidin Synthesis, Solution Structure, Antimicrobial Activities and Synergism, and in Vivo Hepatic Response to Bacterial Infections
  60. K+ Channel Expression during B Cell Differentiation: Implications for Immunomodulation and Autoimmunity
  61. Efficient Asymmetric Synthesis of (S)- and (R)-N-Fmoc-S-Trityl-α-methylcysteine Using Camphorsultam as a Chiral Auxiliary
  62. K+ channels as targets for specific immunomodulation
  63. Rational design and synthesis of selective BACE-1 inhibitors
  64. The voltage-gated Kv1.3 K+ channel in effector memory T cells as new target for MS
  65. The Caspase-like Sites of Proteasomes, Their Substrate Specificity, New Inhibitors and Substrates, and Allosteric Interactions with the Trypsin-like Sites
  66. The voltage-gated Kv1.3 K+ channel in effector memory T cells as new target for MS
  67. An efficient asymmetric synthesis of Fmoc-l-cyclopentylglycine via diastereoselective alkylation of glycine enolate equivalent
  68. A Novel Fluorescent Toxin to Detect and Investigate Kv1.3 Channel Up-regulation in Chronically Activated T Lymphocytes
  69. Mutating a Critical Lysine in ShK Toxin Alters Its Binding Configuration in the Pore−Vestibule Region of the Voltage-Gated Potassium Channel, Kv1.3†
  70. Addition ofo-aminobenzoic acid during Fmoc solid phase synthesis of a fluorogenic substrate containing 3-nitrotyrosine
  71. Designed Peptide Analogues of the Potassium Channel Blocker ShK Toxin †
  72. Selective blockade of T lymphocyte K+channels ameliorates experimental autoimmune encephalomyelitis, a model for multiple sclerosis
  73. Potassium channels in T lymphocytes: toxins to therapeutic immunosuppressants
  74. Structure-guided Transformation of Charybdotoxin Yields an Analog That Selectively Targets Ca2+-activated over Voltage-gated K+ Channels
  75. Role of Disulfide Bonds in the Structure and Potassium Channel Blocking Activity of ShK Toxin†
  76. Structural Conservation of the Pores of Calcium-activated and Voltage-gated Potassium Channels Determined by a Sea Anemone Toxin
  77. Auto-inactivation by cleavage within the dimer interface of kaposi’s sarcoma-associated herpesvirus protease
  78. ShK-Dap22, a Potent Kv1.3-specific Immunosuppressive Polypeptide
  79. Ionisation behaviour and solution properties of the potassium-channel blocker ShK toxin
  80. Secondary structure of ShK toxin, a potassium-channel-blocking peptide
  81. Solution structure of ShK toxin, a novel potassium channel inhibitor from a sea anemone
  82. Identification of Three Separate Binding Sites on SHK Toxin, a Potent Inhibitor of Voltage-Dependent Potassium Channels in Human T-Lymphocytes and Rat Brain
  83. An Essential Binding Surface for ShK Toxin Interaction with Rat Brain Potassium Channels†
  84. Mass spectral analysis of peptides containing nitrobenzyl moieties
  85. Synthesis and structural characterisation of analogues of the potassium channel blocker charybdotoxin
  86. A Continuous Fluorescence-Based Assay of Human Cytomegalovirus Protease Using a Peptide Substrate
  87. Assignment of the three disulfide bonds in ShK toxin: A potent potassium channel inhibitor from the sea anemone Stichodactyla helianthus
  88. A facile method to prepare C-terminal fluorescently labelled peptides by an Fmoc strategy
  89. Three-dimensional Structure in Solution of the Calcium Channel Blocker ω-Conotoxin
  90. Noncompetitive Inhibition of N-Methyl-D-Aspartate by Conantokin-G: Evidence for an Allosteric Interaction at Polyamine Sites
  91. Synthesis and characterization of a disulfide bond isomer of omega-conotoxin GVIA
  92. Isolation, characterization, and amino acid sequence of a polypeptide neurotoxin occurring in the sea anemone Stichodactyla helianthus