کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
6197196 1602606 2013 13 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Novel compstatin family peptides inhibit complement activation by drusen-like deposits in human retinal pigmented epithelial cell cultures
ترجمه فارسی عنوان
پپتید خانواده پستانداران مجله کامپاتین مهار فعال سازی کمپلمان توسط رسوبات مشابه حفره در کشت سلول های اپیتلیال رنگی شبکیه انسان
موضوعات مرتبط
علوم زیستی و بیوفناوری ایمنی شناسی و میکروب شناسی ایمونولوژی و میکروب شناسی (عمومی)
چکیده انگلیسی


- New compstatin family peptide inhibitors of the complement system are designed.
- A human retinal pigmented epithelial (RPE) cell assay is used to test peptide efficacy.
- The peptide sequences are optimized to balance binding and solubility properties.
- Molecular dynamics simulations reveal novel binding features for the new peptides.

We have used a novel human retinal pigmented epithelial (RPE) cell-based model that mimics drusen biogenesis and the pathobiology of age-related macular degeneration to evaluate the efficacy of newly designed peptide inhibitors of the complement system. The peptides belong to the compstatin family and, compared to existing compstatin analogs, have been optimized to promote binding to their target, complement protein C3, and to enhance solubility by improving their polarity/hydrophobicity ratios. Based on analysis of molecular dynamics simulation data of peptide-C3 complexes, novel binding features were designed by introducing intermolecular salt bridge-forming arginines at the N-terminus and at position −1 of N-terminal dipeptide extensions. Our study demonstrates that the RPE cell assay has discriminatory capability for measuring the efficacy and potency of inhibitory peptides in a macular disease environment.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Experimental Eye Research - Volume 116, November 2013, Pages 96-108
نویسندگان
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