表皮生长因子受体
表皮生长因子
对接(动物)
受体
计算生物学
药物发现
体外
生物
药理学
化学
生物化学
医学
护理部
作者
Salvador Guardiola,Mireia Díaz‐Lobo,Jesús Seco,Jesús García,Laura Nevola,Ernest Giralt
出处
期刊:ChemBioChem
[Wiley]
日期:2015-12-17
卷期号:17 (8): 702-711
被引量:24
标识
DOI:10.1002/cbic.201500525
摘要
Epidermal growth factor receptor (EGFR) is a key target in chemotherapy. Some drugs acting on the receptor are currently in use; however, drug resistance, which causes tumour relapse, calls for the discovery of alternative inhibitors. Using docking and receptor hotspot mimicry, we have designed novel peptides directed at EGF, the main growth factor ligand of EGFR. An array of biophysical techniques was used to characterise the structure and interaction of these ligands with the target protein. Both design methods identified peptides able to bind EGF, and the capacity of these peptides to inhibit the interaction between EGF and EGFR was demonstrated in two in vitro systems. Based on targeting the smaller companion of a protein-protein interaction, the new approach described herein can be envisaged as a parallel drug design strategy, and our compounds represent the first in a new class of binders that could serve as complementary compounds in potential multidrug cancer therapy.
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