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Cited by 632

The DOI matches its Crossref record; 55 of the 55 references it cites were found in a registry or an index.

Engineering human ACE2 to optimize binding to the spike protein of SARS coronavirus 2

Open access
Chan, Kui K., Dorosky, Danielle, Sharma, Preeti, Abbasi, Shawn A., Dye, John M., Kranz, David M., Herbert, Andrew S., Procko, Erik·2020·Science

Abstract

A decoy receptor for SARS-CoV-2: For severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) to enter human cells, the spike protein on the surface of the virus must bind to the host receptor protein, angiotensin-converting enzyme 2 (ACE2). A soluble version of the receptor is being explored as a therapeutic. Chan et al. used deep mutagenesis to identify ACE2 mutants that bind more tightly to the spike protein and combined mutations to further increase binding affinity (see the Perspective by DeKosky). A promising variant was engineered to be a stable dimer that has a binding affinity for the spike protein; it is comparable with neutralizing antibodies and neutralized both SARS-CoV-2 and SARS-CoV-1 in a cell-based assay. In addition, the similarity to the natural receptor may limit the possibility for viral escape. Science , this issue p. 1261 ; see also p. 1167

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Metadata

Authors
Chan, K. K., Dorosky, D., Sharma, P., Abbasi, S. A., Dye, J. M., Kranz, D. M., Herbert, A. S., & Procko, E.
Venue
Science
Published
2020-09-04
Volume
369
Issue
6508
Pages
1261-1265
ISSN
  • 0036-8075 (ISSN-L)
  • 1095-9203
OpenAlex
W3047003416
Cited by
632
References
55
FWCI
15.51
Type
journal article
Language
en
Open access
hybrid

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CoChat. (2026). Citation check: Engineering human ACE2 to optimize binding to the spike protein of SARS coronavirus 2. https://app.cochat.ai/papers/10.1126/science.abc0870
The paper
Chan, K. K., Dorosky, D., Sharma, P., Abbasi, S. A., Dye, J. M., Kranz, D. M., Herbert, A. S., & Procko, E. (2020). Engineering human ACE2 to optimize binding to the spike protein of SARS coronavirus 2. Science. https://doi.org/10.1126/science.abc0870

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