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The interaction between the angiotensin-converting enzyme 2 (ACE2) receptor and the receptor binding domain (RBD) of the SARS-CoV-2 spike protein is crucial for viral entry into host cells. ACE2, a membrane-bound carboxypeptidase involved in blood pressure regulation, is exploited by the virus for attachment and subsequent cell entry. This interaction is a primary target for therapeutic intervention, including neutralizing antibodies, small molecule inhibitors, and vaccine design, aimed at disrupting virus-cell fusion and preventing infection.
Inhibition of viral entry by blocking the interaction between the SARS-CoV-2 spike RBD and the ACE2 receptor.
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