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血管紧张素转化酶 2(ACE2)肽酶活性的特性。

Characterizations of angiotensin-converting enzyme-2 (ACE2) peptidase activity.

机构信息

Department of Pharmacology & Physiology, Georgetown University Medical Center, Washington DC 20007, USA.

Department of Pharmacology & Physiology, Georgetown University Medical Center, Washington DC 20007, USA.

出版信息

Arch Biochem Biophys. 2024 Nov;761:110167. doi: 10.1016/j.abb.2024.110167. Epub 2024 Sep 28.

Abstract

Angiotensin (Ang) II (1-8) is a potent vasoconstrictor known for its role in hypertension. Angiotensin-converting enzyme (ACE2) converts Ang II (1-8) to a vasodilator Ang (1-7) by removing the carboxy-terminal Phe. ACE2 more recently gained attention as the receptor for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) that caused the coronavirus disease 2019 (COVID-19) pandemic. Given the pathophysiological importance of ACE2, the present study examined the mechanism of ACE2 catalytic activity by comparing the ability of angiotensin molecules of various lengths to compete with the artificial fluorogenic substrate. The Fluorimetric SensoLyte 390 ACE2 Activity Assay uses an Mca/Dnp fluorescence resonance energy transfer peptide as the substrate. Results showed that the natural substrate Ang II (1-8) competed with the fluorogenic substrate, reducing the fluorescence signals. Deletion of C-terminal Phe resulted in the loss of the ability to compete with the artificial substrate, as shown by the actions of Ang (1-7), Ang (2-7), and Ang (5-7). By contrast, the loss of N-terminal Asp potentiated the ability to compete with the substrate as seen by the action of Ang III (2-8). However, the loss of two amino acids (Asp-Arg) from the N-terminus reduced the ability to compete with the substrate as observed by the actions of Ang IV (3-8) and Ang (5-8). Ang I (1-10) and Ang (1-9) did not strongly compete with the substrate. Interestingly, shorter peptides Ang (1-5) and Ang (1-4) potentiated the ACE2 activity. These results suggest that Ang II and Ang III are the best natural substrates for ACE2.

摘要

血管紧张素(Ang)II(1-8)是一种强效血管收缩剂,已知其在高血压中的作用。血管紧张素转换酶(ACE2)通过去除羧基末端苯丙氨酸将 Ang II(1-8)转化为血管扩张剂 Ang(1-7)。ACE2 最近因其作为严重急性呼吸系统综合征冠状病毒 2(SARS-CoV-2)的受体而受到关注,SARS-CoV-2 导致了 2019 年冠状病毒病(COVID-19)大流行。鉴于 ACE2 的病理生理学重要性,本研究通过比较各种长度的血管紧张素分子与人工荧光底物竞争的能力来检查 ACE2 催化活性的机制。荧光敏度 390 ACE2 活性测定法使用 Mca/Dnp 荧光共振能量转移肽作为底物。结果表明,天然底物 Ang II(1-8)与荧光底物竞争,降低了荧光信号。C 末端苯丙氨酸的缺失导致其丧失与人工底物竞争的能力,如 Ang(1-7)、Ang(2-7)和 Ang(5-7)的作用所示。相比之下,N 末端天冬氨酸的缺失增强了与底物竞争的能力,如 Ang III(2-8)的作用所示。然而,从 N 末端缺失两个氨基酸(天冬氨酸-精氨酸),如 Ang IV(3-8)和 Ang(5-8)的作用所示,降低了与底物竞争的能力。Ang I(1-10)和 Ang(1-9)不能与底物强烈竞争。有趣的是,较短的肽 Ang(1-5)和 Ang(1-4)增强了 ACE2 的活性。这些结果表明,Ang II 和 Ang III 是 ACE2 的最佳天然底物。

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