Development of Highly Selective Kv1.3-Blocking PeptidesBased on the Sea Anemone Peptide ShK

Marine Drugs

Redwan Huq¹  Rajeev B. Tajhya¹  Christine Beeton¹  Sandeep Chhabra²  Raymond S. Norton²  Shih Chieh Chang²  Michael W. Pennington³  Satendra Chauhan³ 

[1] Department of Molecular Physiology and Biophysics, Baylor College of Medicine,One Baylor Plaza, Houston, TX 77030, USA;Medicinal Chemistry, Monash Institute of Pharmaceutical Sciences, Monash University, Parkville, VIC 3052, Australia;Peptides International Inc., 11621 Electron Drive, Louisville, KY 40065, USA;

关键词: immunomodulator;    T lymphocyte;    potassium channel;    disulfide-rich peptide;    sea anemone toxin;    K+ channel blocker;   

DOI  :  10.3390/md13010529

来源: DOAJ

【 摘 要 】

ShK, from the sea anemone Stichodactyla helianthus, is a 35-residuedisulfide-rich peptide that blocks the voltage-gated potassium channel Kv1.3 at ca. 10 pM and the related channel Kv1.1 at ca. 16 pM. We developed an analog of this peptide,ShK-186, which is currently in Phase 1b-2a clinical trials for the treatment of autoimmune diseases such as multiple sclerosis and rheumatoid arthritis. While ShK-186 displaysa >100-fold improvement in selectivity for Kv1.3 over Kv1.1 compared with ShK, there is considerable interest in developing peptides with an even greater selectivity ratio. In this report, we describe several variants of ShK that incorporate p-phophono-phenylalanine at the N-terminus coupled with internal substitutions at Gln16 and Met21. In addition, we also explored the combinatorial effects of these internal substitutions with an alanine extension at the C-terminus. Their selectivity was determined by patch-clamp electrophysiology on Kv1.3 and Kv1.1 channels stably expressed in mouse fibroblasts. The peptides with an alanine extension blocked Kv1.3 at low pM concentrations and exhibited up to 2250-fold selectivity for Kv1.3 over Kv1.1. Analogs that incorporates p-phosphono-phenylalanine at the N-terminus blocked Kv1.3 with IC50s in the low pM range and did not affect Kv1.1 at concentrations up to 100 nM, displaying a selectivity enhancement of >10,000-fold for Kv1.3 over Kv1.1. Other potentially important Kv channels such as Kv1.4 and Kv1.6 were only partially blocked at 100 nM concentrations of each of the ShK analogs.

【 授权许可】

Unknown