Interaction Between Vpx and SAMHD1, Vital for SAMHD1 Inhibition.

IF 1.5 4区 医学 Q4 IMMUNOLOGY
AIDS research and human retroviruses Pub Date : 2024-06-01 Epub Date: 2023-12-26 DOI:10.1089/AID.2023.0052
Zahra Hasanshahi, Behzad Dehghani, Ava Hashempour
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引用次数: 0

Abstract

It was confirmed that the sterile alpha motif and HD domain 1 (SAMHD1) limits human immunodeficiency virus type 1 (HIV-1) replication. In contrast, viral protein x (Vpx) in HIV-2 and some simian immunodeficiency viruses can counteract this effect. The possible interaction between SAMHD1 and Vpx was suggested by previous studies; however, there are no data to confirm this interaction. Therefore, this study aimed to study the interaction between two proteins and the properties of Vpx protein for the first time using bioinformatic tools. Vpx and SAMHD1 sequences were obtained from the National Center for Biotechnology Information GenBank. Several software were used to define Vpx properties and the interaction between Vpx and different SAMHD1 isoforms. Our findings indicated the difference in interaction sites among different Vpx. However, in all Vpx proteins, this region is from amino acids 4 to 90. In addition, two regions (26-31 and 134-139) and two amino acids 425 and 429 in SAMHD1 are vital in the possible interaction. In addition, our analysis determined the physicochemical and immunological properties of the Vpx. Considering all factors, this study could confirm that Vpx interacts with SAMHD1, which could inhibit SAMHD1. Moreover, our findings can pave the way for future studies to express and purify Vpx in the laboratory and study this protein in vitro.

Vpx 与 SAMHD1 之间的相互作用,对 SAMHD1 的抑制作用至关重要。
研究证实,SAMHD1 限制了 HIV-1 的复制。与此相反,HIV-2 和一些猿类免疫缺陷病毒(SIV)中的 Vpx 蛋白却能抵消这种作用。以前的研究表明,SAMHD1 和 Vpx 之间可能存在相互作用,但目前还没有数据证实这种相互作用。因此,本研究旨在利用生物信息学工具首次研究两种蛋白之间的相互作用以及 Vpx 蛋白的特性。Vpx 和 SAMHD1 的序列来自 NCBI GenBank。研究人员使用多种软件定义了Vpx的特性以及Vpx与不同SAMHD1异构体之间的相互作用。我们的研究结果表明,不同 Vpx 蛋白的相互作用位点存在差异。然而,在所有 Vpx 蛋白中,该区域位于第 4 至 90 个氨基酸之间。此外,SAMHD1 中的两个区域(26-31 和 134-139)和两个氨基酸 425 和 429 在可能的相互作用中也至关重要。此外,我们的分析还确定了 Vpx 蛋白的理化和免疫学特性。综合考虑各种因素,本研究可以证实 Vpx 与 SAMHD1 相互作用,从而抑制 SAMHD1。此外,我们的研究结果还为今后在实验室中表达和纯化 Vpx 蛋白并对其进行体外研究铺平了道路。
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来源期刊
CiteScore
3.10
自引率
6.70%
发文量
201
审稿时长
3-6 weeks
期刊介绍: AIDS Research and Human Retroviruses was the very first AIDS publication in the field over 30 years ago, and today it is still the critical resource advancing research in retroviruses, including AIDS. The Journal provides the broadest coverage from molecular biology to clinical studies and outcomes research, focusing on developments in prevention science, novel therapeutics, and immune-restorative approaches. Cutting-edge papers on the latest progress and research advances through clinical trials and examination of targeted antiretroviral agents lead to improvements in translational medicine for optimal treatment outcomes. AIDS Research and Human Retroviruses coverage includes: HIV cure research HIV prevention science - Vaccine research - Systemic and Topical PreP Molecular and cell biology of HIV and SIV Developments in HIV pathogenesis and comorbidities Molecular biology, immunology, and epidemiology of HTLV Pharmacology of HIV therapy Social and behavioral science Rapid publication of emerging sequence information.
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