人小窝蛋白-1:前列腺癌治疗的有效抑制剂:计算方法

Uzma Khanam, B. K. Malik, P. Mathur, B. Rathi
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摘要

Caveolin-1 (Cav-1)是一种22 kDa的小泡蛋白,在小泡膜内起支架作用,与g α-蛋白相互作用,从而调节其活性。早期研究报道前列腺癌患者血清中小窝蛋白-1水平升高。前列腺癌患者分泌的Cav-1促进血管生成、细胞增殖和抗凋亡活性。本研究旨在利用计算方法探索Cav-1作为前列腺癌治疗的靶点。通过分子对接、结构碱分子模拟和分子动力学模拟等方法对Cav-1抑制剂进行研究。利用预测模型对含锌生物源化合物数据库进行虚拟筛选。利用IFD和100ns长的分子动力学模拟对Cav-1活性位点残基的稳定性进行了评价。所报道的化合物显示出显著的结合,因此可以认为是Cav-1的有效治疗抑制剂。因此,对Cav-1的生化相互作用的进一步调查研究将为其可能的治疗应用提供有价值的见解。
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Human caveolin-1 a potent inhibitor for prostate cancer therapy: a computational approach
Caveolin-1 (Cav-1) is 22 kDa caveolae protein, acts as a scaffold within caveolar membranes, interacts with Gα-protein and thereby regulates their activity. Earlier studies reported elevated caveolin-1 levels in the serum of prostate cancer patients. Secreted Cav-1 promotes angiogenesis, cell proliferation and anti-apoptotic activities in prostate cancer patients. This study was designed to explore Cav-1 as a target for prostate cancer therapy using computational approach. Molecular docking, structural base molecular modelling and molecular dynamics simulations were performed to investigate Cav-1 inhibitors. A predictive model was used for virtual screening against ZINC database of biogenic compounds. Stability of the active site residues of Cav-1 was estimated by IFD and 100 ns long molecular dynamic simulations. The reported compounds showed significant binding and thus can be considered potent therapeutic inhibitors of Cav-1. Thus, further investigative studies on the biochemical interactions of Cav-1 would provide a valuable insight into its probable therapeutic applications.
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