Bioinformatics Prediction of Interaction Silver Nanoparticles on the Disulfide Bonds of HIV-1 Gp120 Protein

S. Gavanji, H. Mohabbatkar, H. Baghshahi, A. Zarrabi
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引用次数: 5

Abstract

Silver nanoparticles have anti-HIV features in early stages of virus amplification. The two existing disulfide bonds in carboxyl half of the HIV-1 GP120, which cooperate in conjugation of CD4 receptor, interact with silver nanoparticles. Studies on protein disulfide bonds were done using Metal Detector Predicts V2.0 software. All Cys and His residues in amino acid sequences were identified. Protein denaturation decreases disulfide bonds when silver ions couple with sulfhydryl groups. CTRPNNNTRKRIRIQRGPGRAFVTIGKIGNMRQAHC amino acid sequence in GP 120 plays a key role. Breaking this bond can alter spatial structure of the protein and prevents this part from connecting to CD4. Ultimately, nanosilver can prevent HIV from connecting to CD4.
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银纳米粒子对HIV-1 Gp120蛋白二硫键相互作用的生物信息学预测
银纳米颗粒在病毒扩增的早期阶段具有抗hiv的特征。在HIV-1 GP120的羧基一半中存在两个二硫键,它们合作结合CD4受体,与银纳米粒子相互作用。蛋白质二硫键的研究是用金属探测器预测V2.0软件完成的。鉴定了氨基酸序列中所有的Cys和His残基。当银离子与巯基偶联时,蛋白质变性会减少二硫键。ctrpnnnntrkririqrgpgrafvtigkignmrqahc氨基酸序列在GP 120中起关键作用。打破这个键可以改变蛋白质的空间结构,阻止这部分连接到CD4。最终,纳米银可以阻止HIV与CD4细胞连接。
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