Peptide-Based Inhibitors of Protein-Protein Interactions (PPIs): A Case Study on the Interaction Between SARS-CoV-2 Spike Protein and Human Angiotensin-Converting Enzyme 2 (hACE2).

IF 3.9 3区 工程技术 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Biomedicines Pub Date : 2024-10-16 DOI:10.3390/biomedicines12102361
Aizhan Rakhmetullina, Piotr Zielenkiewicz, Norbert Odolczyk
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Abstract

Protein-protein interactions (PPIs) are fundamental to many critical biological processes and are crucial in mediating essential cellular functions across diverse organisms, including bacteria, parasites, and viruses. A notable example is the interaction between the SARS-CoV-2 spike (S) protein and the human angiotensin-converting enzyme 2 (hACE2), which initiates a series of events leading to viral replication. Interrupting this interaction offers a promising strategy for blocking or significantly reducing infection, highlighting its potential as a target for anti-SARS-CoV-2 therapies. This review focuses on the hACE2 and SARS-CoV-2 spike protein interaction, exemplifying the latest advancements in peptide-based strategies for developing PPI inhibitors. We discuss various approaches for creating peptide-based inhibitors that target this critical interaction, aiming to provide potential treatments for COVID-19.

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基于肽的蛋白质-蛋白质相互作用(PPIs)抑制剂:SARS-CoV-2 Spike 蛋白与人血管紧张素转换酶 2 (hACE2) 相互作用的案例研究》。
蛋白质与蛋白质之间的相互作用(PPIs)是许多关键生物过程的基础,对于介导包括细菌、寄生虫和病毒在内的各种生物体的基本细胞功能至关重要。一个显著的例子是 SARS-CoV-2 棘波(S)蛋白与人类血管紧张素转换酶 2(hACE2)之间的相互作用,这种相互作用引发了一系列导致病毒复制的事件。中断这种相互作用为阻断或显著减少感染提供了一种有前景的策略,突出了其作为抗 SARS-CoV-2 疗法靶点的潜力。本综述将重点讨论 hACE2 与 SARS-CoV-2 棘蛋白的相互作用,展示基于多肽的 PPI 抑制剂开发策略的最新进展。我们讨论了针对这一关键相互作用开发肽基抑制剂的各种方法,旨在为 COVID-19 提供潜在的治疗方法。
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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来源期刊
Biomedicines
Biomedicines Biochemistry, Genetics and Molecular Biology-General Biochemistry,Genetics and Molecular Biology
CiteScore
5.20
自引率
8.50%
发文量
2823
审稿时长
8 weeks
期刊介绍: Biomedicines (ISSN 2227-9059; CODEN: BIOMID) is an international, scientific, open access journal on biomedicines published quarterly online by MDPI.
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