The Integrin Binding Peptide, ATN-161, as a Novel Therapy for SARS-CoV-2 Infection.
JACC Basic Transl Sci
; 6(1): 1-8, 2021 Jan.
Article
in English
| MEDLINE | ID: covidwho-866798
Preprint
This scientific journal article is probably based on a previously available preprint. It has been identified through a machine matching algorithm, human confirmation is still pending.
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This scientific journal article is probably based on a previously available preprint. It has been identified through a machine matching algorithm, human confirmation is still pending.
See preprint
ABSTRACT
Many efforts to design and screen therapeutics for the current severe acute respiratory syndrome-coronavirus-2 (SARS-CoV-2) pandemic have focused on inhibiting viral host cell entry by disrupting angiotensin-converting enzyme-2 (ACE2) binding with the SARS-CoV-2 spike protein. This work focuses on the potential to inhibit SARS-CoV-2 entry through a hypothesized α5ß1 integrin-based mechanism and indicates that inhibiting the spike protein interaction with α5ß1 integrin (+/- ACE2) and the interaction between α5ß1 integrin and ACE2 using a novel molecule (ATN-161) represents a promising approach to treat coronavirus disease-19.
ACE2; ACE2, angiotensin-converting enzyme 2; ATN-161; CO2, carbon dioxide; COVID-19; COVID-19, coronavirus disease-2019; DMEM, Dulbecco's modified eagle media; ELISA, enzyme-linked immunosorbent assay; IC50, half-maximal inhibitory concentration; RBD, receptor binding domain; RGD, arginine-glycine-aspartate; SARS-CoV-2; SARS-CoV-2, severe acute respiratory syndrome-coronavirus-2; alpha5beta1 integrin; hACE2, human angiotensin-converting enzyme 2; host-cell entry; qPCR, quantitative polymerase chain reaction; receptor binding domain; therapeutic; viral spike protein
Full text:
Available
Collection:
International databases
Database:
MEDLINE
Language:
English
Journal:
JACC Basic Transl Sci
Year:
2021
Document Type:
Article
Affiliation country:
J.jacbts.2020.10.003
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