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ACE2, the Receptor that Enables Infection by SARS-CoV-2: Biochemistry,Structure, Allostery and Evaluation of the Potential Development of ACE2 Modulators
Authors:Lissy Z F Gross  Mariana Sacerdoti  Prof Albrecht Piiper  Prof Stefan Zeuzem  Dr Alejandro E Leroux  Dr Ricardo M Biondi
Affiliation:1. Chemical Biology of Regulatory Mechanisms, IBioBA-CONICET-Partner Institute of the Max Planck Society, Godoy Cruz 2390, Buenos Aires, Argentina

These authors contributed equally to this work.;2. Internal Medicine I, Frankfurt University Hospital, Theodor-Stern-Kai 7, Frankfurt am Main, Germany;3. Chemical Biology of Regulatory Mechanisms, IBioBA-CONICET-Partner Institute of the Max Planck Society, Godoy Cruz 2390, Buenos Aires, Argentina

Abstract:Angiotensin converting enzyme 2 (ACE2) is the human receptor that interacts with the spike protein of coronaviruses, including the one that produced the 2020 coronavirus pandemic (COVID-19). Thus, ACE2 is a potential target for drugs that disrupt the interaction of human cells with SARS-CoV-2 to abolish infection. There is also interest in drugs that inhibit or activate ACE2, that is, for cardiovascular disorders or colitis. Compounds binding at alternative sites could allosterically affect the interaction with the spike protein. Herein, we review biochemical, chemical biology, and structural information on ACE2, including the recent cryoEM structures of full-length ACE2. We conclude that ACE2 is very dynamic and that allosteric drugs could be developed to target ACE2. At the time of the 2020 pandemic, we suggest that available ACE2 inhibitors or activators in advanced development should be tested for their ability to allosterically displace the interaction between ACE2 and the spike protein.
Keywords:ACE2  allostery  coronavirus  drug development  protein dynamics
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