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Indigo plant leaf extract inhibits the binding of SARS-CoV-2 spike protein to angiotensin-converting enzyme 2.

Authors :
Hagiyama, Man
Takeuchi, Fuka
Sugano, Aki
Yoneshige, Azusa
Inoue, Takao
Wada, Akihiro
Kajiyama, Hiroshi
Takaoka, Yutaka
Sasaki, Kenroh
Ito, Akihiko
Source :
Experimental & Therapeutic Medicine. Apr2022, Vol. 23 Issue 4, pN.PAG-N.PAG. 1p.
Publication Year :
2022

Abstract

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) uses its S1 spike protein to bind to angiotensin-converting enzyme 2 (ACE2) on human cells in the first step of cell entry. Tryptanthrin, extracted from leaves of the indigo plant, Polygonum tinctorium, using d-limonene (17.3 µg/ml), is considered to inhibit ACE2-mediated cell entry of another type of coronavirus, HCoV-NL63. The current study examined whether this extract could inhibit the binding of the SARS-CoV-2 spike protein to ACE2. Binding was quantified as cell-bound fluorescence intensity in live cell cultures in which canine kidney MDCK cells overexpressing ACE2 were incubated with fluorescein-labeled S1 spike protein. When indigo extract, together with S1 protein, was added at 8,650x and 17,300x dilutions, fluorescence intensity decreased in a dose- and S1 extract-dependent manner, without affecting cell viability. When 4.0-nM tryptanthrin was added instead of the indigo extract, fluorescence intensity also decreased, but to a lesser degree than with indigo extract. Docking simulation analyses revealed that tryptanthrin readily bound to the receptor-binding domain of the S1 protein, and identified 2- and 7-amino acid sequences as the preferred binding sites. The indigo extract appeared to inhibit S1-ACE2 binding at high dilutions, and evidently contained other inhibitory elements as well as tryptanthrin. This extract may be useful for the prevention or treatment of SARS-CoV-2 infection. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
17920981
Volume :
23
Issue :
4
Database :
Academic Search Index
Journal :
Experimental & Therapeutic Medicine
Publication Type :
Academic Journal
Accession number :
156029422
Full Text :
https://doi.org/10.3892/etm.2022.11200