[Development of an engineered ACE2 decoy for COVID-19 therapy.]

Uirusu Pub Date : 2023-01-01 DOI:10.2222/jsv.73.163
Toru Okamoto, Yumi Itoh, Tatsuya Suzuki
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Abstract

It has been passed four years since the pandemic caused by the severe acute respiratory syndrome-2 (SARS-CoV-2) that began in 2019. Since June 2020, we have been working on a project to develop a therapeutic drug using receptor decoys, even though we cannot predict how long the pandemic will last or how long our daily lives will be restricted. This receptor decoy utilizes Angiotensin-converting enzyme 2 (ACE2), which is the receptor for SARS-CoV-2, and involves introducing mutations that enhance its binding ability with the spike protein of SARS-CoV-2. This high-affinity ACE2, acting as a decoy protein, is a strategy to inhibit viral infection and to expect therapeutic effects by replacing the endogeneous ACE2 that SARS-CoV-2 binds to with ACE2 decoy. This paper introduces the development of ACE2 decoys that have progressed through collaborative research with many researchers outside the field of virology.

[开发用于COVID-19疗法的工程化ACE2诱饵]
由严重急性呼吸系统综合征-2(SARS-CoV-2)引起的大流行始于 2019 年,至今已过去四年。自 2020 年 6 月以来,尽管我们无法预测大流行会持续多久,也无法预测我们的日常生活会受到多长时间的限制,但我们一直致力于利用受体诱饵开发治疗药物的项目。这种受体诱饵利用血管紧张素转换酶 2(ACE2)作为 SARS-CoV-2 的受体,并通过引入突变增强其与 SARS-CoV-2 的尖峰蛋白的结合能力。这种高亲和力 ACE2 作为诱饵蛋白,是一种抑制病毒感染的策略,通过用 ACE2 诱饵取代 SARS-CoV-2 与之结合的内源性 ACE2,可望产生治疗效果。本文介绍了通过与病毒学领域以外的许多研究人员合作研究,ACE2 诱饵的开发进展情况。
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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