Novel compstatin family peptides inhibit complement activation by drusen-like deposits in human retinal pigmented epithelial cell cultures

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• 作者：Ronald D. Gorham Jr. ; David L. Forest ; Phanourios Tamamis ; Aliana L贸pez de Victoria ; M谩rta Kraszni ; Chris A. Kieslich ; Christopher D. Banna ; Meghan L. Bellows-Peterson ; Cynthia K. Larive ; Christodoulos A. Floudas ; Georgios Archontis ; Lincoln V. Johnson ; Dimitrios Morikis
• 关键词：macular degeneration ; drusen ; retinal pigmented epithelium ; complement system ; complement inhibitors ; compstatin family peptides ; molecular dynamics
• 刊名：Experimental Eye Research
• 出版年：November, 2013
• 年：2013
• 卷：116
• 期：Complete
• 页码：96-108
• 全文大小：3056 K

文摘

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聽鈭? 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.