Structure based sequence analysis & epitope prediction of gp41 HIV1 envelope glycoprotein isolated in Pakistan.

Syyada Samra Jafri, Saliha Kiran, Syed Babar Jamal, Masaud Shah
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引用次数: 2

Abstract

Unlabelled:

Background: Gp41 is an envelope glycoprotein of human immune deficiency virus (HIV). HIV viral glycoprotein gp41, present in complex with gp120, assists the viral entry into host cell. Over eighty thousands individuals are HIV infected in Pakistan which makes about 0.2% of 38.6 million infected patients worldwide. Hence, HIV gp41 protein sequences isolated in Pakistan were analyzed for the CD4 and CD8 T cells binding epitopes.

Results: Immunoinformatics tools were applied for the study of variant region of HIV gp41envelope protein. The protein nature was analyzed using freely accessible computational software. About 90 gp41 sequences of Pakistani origin were aligned and variable and conserved regions were found. Four segments were found to be conserved in gp41 viral protein. A method was developed, involving the secondary structure, surface accessibility, hydrophobicity, antigenicity and molecular docking for the prediction and location of epitopes in the viral glycoprotein. Some highly conserved CD4 and CD8 binding epitopes were also found using multiple parameters. The predicted continuous epitopes mostly fall in the conserved region of 1-12; 14-22 and 25-46 and can be used as effective vaccine candidates.

Conclusions: The study revealed potential HIV subtype a derived cytotoxic T cell (CTL) epitopes from viral proteome of Pakistani origin. The conserved epitopes are very useful for the diagnosis of the HIV 1 subtype a. This study will also help scientists to promote research for vaccine development against HIV 1 subtype a, isolated in Pakistan.

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巴基斯坦hiv - 1包膜糖蛋白gp41结构序列分析及表位预测。
背景:Gp41是人类免疫缺陷病毒(HIV)的包膜糖蛋白。HIV病毒糖蛋白gp41与gp120复合存在,有助于病毒进入宿主细胞。巴基斯坦有8万多人感染了艾滋病毒,占全球3860万感染者的0.2%。因此,分析在巴基斯坦分离的HIV gp41蛋白序列的CD4和CD8 T细胞结合表位。结果:应用免疫信息学工具对艾滋病病毒gp41包膜蛋白变异区进行了研究。使用可自由访问的计算软件分析蛋白质的性质。对大约90个巴基斯坦来源的gp41序列进行了比对,发现了可变和保守区。发现gp41病毒蛋白中有四个片段是保守的。开发了一种预测和定位病毒糖蛋白表位的方法,包括二级结构、表面可及性、疏水性、抗原性和分子对接。使用多种参数还发现了一些高度保守的CD4和CD8结合表位。预测的连续表位大多落在1-12的保守区;14-22和25-46,并且可以用作有效的候选疫苗。结论:该研究从巴基斯坦来源的病毒蛋白质组中揭示了潜在的HIV亚型衍生的细胞毒性T细胞(CTL)表位。保守的表位对HIV 1亚型a的诊断非常有用。这项研究还将帮助科学家促进针对在巴基斯坦分离的HIV 1亚类型a的疫苗开发研究。
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