Characterization and Structural Prediction of Proteins in SARS-CoV-2 Bangladeshi Variant Through Bioinformatics.

Microbiology insights Pub Date : 2022-08-09 eCollection Date: 2022-01-01 DOI:10.1177/11786361221115595
Pinky Debnath, Umama Khan, Md Salauddin Khan
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Abstract

The renowned respiratory disease induced by the severe acute respiratory syndrome-coronavirus-2 (SARS-CoV-2) has become a global epidemic in just less than a year by the first half of 2020. The subsequent efficient human-to-human transmission of this virus eventually affected millions of people worldwide. The most devastating thing is that the infection rate is continuously uprising and resulting in significant mortality especially among the older age population and those with health co-morbidities. This enveloped, positive-sense RNA virus is chiefly responsible for the infection of the upper respiratory system. The virulence of the SARS-CoV-2 is mostly regulated by its proteins such as entry to the host cell through fusion mechanism, fusion of infected cells with neighboring uninfected cells to spread virus, inhibition of host gene expression, cellular differentiation, apoptosis, mitochondrial biogenesis, etc. But very little is known about the protein structures and functionalities. Therefore, the main purpose of this study is to learn more about these proteins through bioinformatics approaches. In this study, ORF10, ORF7b, ORF7a, ORF6, membrane glycoprotein, and envelope protein have been selected from a Bangladeshi Corona-virus strain G039392 and a number of bioinformatics tools (MEGA-X-V10.1.7, PONDR, ProtScale, ProtParam, SCRIBER, NetSurfP v2.0, IntFOLD, UCSF Chimera, and PyMol) and strategies were implemented for multiple sequence alignment and phylogeny analysis with 9 different variants, predicting hydropathicity, amino acid compositions, protein-binding propensity, protein disorders, and 2D and 3D protein modeling. Selected proteins were characterized as highly flexible, structurally and electrostatically extremely stable, ordered, biologically active, hydrophobic, and closely related to proteins of different variants. This detailed information regarding the characterization and structure of proteins of SARS-CoV-2 Bangladeshi variant was performed for the first time ever to unveil the deep mechanism behind the virulence features. And this robust appraisal also paves the future way for molecular docking, vaccine development targeting these characterized proteins.

通过生物信息学分析 SARS-CoV-2 孟加拉变种蛋白质的特征和结构预测
到 2020 年上半年,由严重急性呼吸系统综合征--冠状病毒 2 型(SARS-CoV-2)诱发的知名呼吸道疾病在短短不到一年的时间里已成为全球性流行病。随后,这种病毒在人与人之间的高效传播最终影响到全球数百万人。最具破坏性的是,感染率持续上升,并导致大量死亡,尤其是在老年人群和患有并发症的人群中。这种有包膜的正义 RNA 病毒主要感染上呼吸道系统。SARS-CoV-2 的毒力主要受其蛋白质调控,如通过融合机制进入宿主细胞、受感染细胞与邻近未感染细胞融合以传播病毒、抑制宿主基因表达、细胞分化、细胞凋亡、线粒体生物生成等。但人们对这些蛋白质的结构和功能知之甚少。因此,本研究的主要目的是通过生物信息学方法进一步了解这些蛋白质。本研究选取孟加拉电晕病毒 G039392 株系中的 ORF10、ORF7b、ORF7a、ORF6、膜糖蛋白和包膜蛋白,并使用多种生物信息学工具(MEGA-X-V10.1.7、PONDR、ProtScale、ProtParam、SCRIBER、NetSurfP v2.0、IntFOLD、UCSF Chimera 和 PyMol),并实施了多序列比对和 9 种不同变体的系统发育分析策略,预测了水合性、氨基酸组成、蛋白质结合倾向、蛋白质紊乱以及二维和三维蛋白质建模。所选蛋白质的特点是高度灵活、结构和静电极其稳定、有序、具有生物活性、疏水性以及与不同变体的蛋白质密切相关。这些有关 SARS-CoV-2 孟加拉变体蛋白质特征和结构的详细信息是有史以来第一次进行的,从而揭示了其毒力特征背后的深层机制。这一有力的评估也为今后针对这些特征蛋白的分子对接和疫苗开发铺平了道路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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