Structure-Based Design of Peptides Targeting VEGF/VEGFRs

被引:1
|
作者
Di Stasi, Rossella [1 ]
De Rosa, Lucia [1 ]
D'Andrea, Luca Domenico [2 ]
机构
[1] CNR, Ist Biostrutture & Bioimmagini, (RDS ), I-80131 Naples, Italy
[2] CNR, Ist Sci & Tecnol Chim G Natta, I-20131 Milan, Italy
关键词
peptide; VEGF; VEGF receptor; peptide design; antiangiogenic; protein binding epitopes; receptor binder; molecular mimicry; ENDOTHELIAL GROWTH-FACTOR; BETA-HAIRPIN; RECEPTOR-BINDING; ALPHA/BETA-PEPTIDES; CRYSTAL-STRUCTURE; HIGH-AFFINITY; VEGF; ANGIOGENESIS; DOMAIN; DISCOVERY;
D O I
10.3390/ph16060851
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Vascular endothelial growth factor (VEGF) and its receptors (VEGFRs) play a main role in the regulation of angiogenesis and lymphangiogenesis. Furthermore, they are implicated in the onset of several diseases such as rheumatoid arthritis, degenerative eye conditions, tumor growth, ulcers and ischemia. Therefore, molecules able to target the VEGF and its receptors are of great pharmaceutical interest. Several types of molecules have been reported so far. In this review, we focus on the structure-based design of peptides mimicking VEGF/VEGFR binding epitopes. The binding interface of the complex has been dissected and the different regions challenged for peptide design. All these trials furnished a better understanding of the molecular recognition process and provide us with a wealth of molecules that could be optimized to be exploited for pharmaceutical applications.
引用
收藏
页数:19
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