key: cord-0755619-rgn0kfam
authors: Liu, Pan; Xie, Xinfang; Gao, Li; Jin, Jing
title: His345 mutant of angiotensin-converting enzyme 2 (ACE2) remains enzymatically active against angiotensin II
date: 2021-04-13
journal: Proc Natl Acad Sci U S A
DOI: 10.1073/pnas.2023648118
sha: e3ed67eb3e7842a19a611c975866b6a7ec550bd2
doc_id: 755619
cord_uid: rgn0kfam

nan

His345mutantofangiotensin-convertingenzyme2 (ACE2) remains enzymatically active against angiotensin II Pan Liu a , Xinfang Xie a , Li Gao a , and Jing Jin a,1  Glasgow et al. (1) report their mutagenesis survey of ACE2 traps for treatment of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). The virus invades human cells via host ACE2 receptor, and strategies aimed at disrupting this process are being explored. As compared to monoclonal antibodies and targeted vaccines that are prone to mutational escape of the virus, the ACE2 trap strategy has unique advantages and was shown to be efficacious in experimental and clinical tests (2, 3) . Current studies, including Glasgow et al., focus on further improvements through alternative designs. These include extending in vivo half-life with an Fc tag (4, 5) , increasing Spike-binding affinity via mutagenesis (1, 6) , and inactivating ACE2 peptidase activity (1, 4) . The Glasgow study combined all three approaches in their lead design (1).

The enzymatic inactivation strategy has two potential benefits: eliminating unwanted cardiovascular side effects attributable to dysregulation of vasoactive hormones, including angiotensin II (Ang II), and permitting high therapeutic doses without oversupplying ACE2 peptidase activity. It is unfortunate that many researchers, including Glasgow In parallel to the Glasgow et al.

(1) study, our group conducted a mutagenesis survey of ACE2-Fc toward inactivating its activity against physiologic substrates (8) . We included mutations intended to disrupt either Zn 2+ binding (via His374, His378, and Glu402) or substrate catalysis (via Glu145, Arg273, His345, Pro346, Asp368, and His505) with alanine substitutions of individual residues. We performed both Mca-APK-DNP assay and phenylalanine hydrolysis measurement using Ang II and Apelin-13 as substrates. Our results show a clear substrate-dependent inactivation among the mutants. Specifically, H345A, P346A, and H505A mutants show complete inactivation of ACE2-Fc against Mca-APK-DNP but intact catalysis against Ang II and Apelin-13. With respect to the H345 mutant (mutated to alanine in our study instead of to leucine as in Glasgow et al.), our results suggest the enzyme can still catalyze Ang II, which is a concern in therapeutic design for SARS-CoV-2.

To ascertain our findings, we repeated the assays and obtained similar results as before (Fig. 1B) . In addition, we performed mass spectrometry to measure the generation of Ang(1-7) by ACE2-Fc R273A and H345A. The results confirm full activity of H345A toward Ang II (Fig. 1C) , which argues against the conclusion by (1) . However, ACE2-Fc enzymatic activity measured by Ang II showed different results, with H345A having full activity as compared to wild-type ACE2-Fc (Right). Meanwhile, R273A showed loss of activity against Ang II. (C) To further confirm the specificity of the reaction, we conducted mass spectrometry analysis of the peptide(s) generated from the reactions, using Ang II peptide as substrate, that further confirmed the loss of activity by R273A mutation, whereas H345A of ACE2 remained fully active.

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