Gain-of-function assay for SARS-CoV-2 M pro inhibition in living cells
The main protease, M pro , of SARS-CoV-2 is required to cleave the viral polyprotein into precise functional units for virus replication and pathogenesis. Here we demonstrate a quantitative reporter for M pro function in living cells, in which protease inhibition by genetic or chemical methods results in strong eGFP fluorescence. This robust gain-of-function system readily distinguishes between inhibitor potencies and can be scaled-up to high-throughput platforms for drug testing.
Errataetall: | |
---|---|
Medienart: |
E-Artikel |
Erscheinungsjahr: |
2020 |
---|---|
Erschienen: |
2020 |
Enthalten in: |
Zur Gesamtaufnahme - year:2020 |
---|---|
Enthalten in: |
bioRxiv : the preprint server for biology - (2020) vom: 09. Nov. |
Sprache: |
Englisch |
---|
Beteiligte Personen: |
Moghadasi, Seyad Arad [VerfasserIn] |
---|
Links: |
---|
Themen: |
---|
Anmerkungen: |
Date Revised 03.05.2023 published: Electronic UpdateIn: mBio. 2022 Jun 28;13(3):e0078422. - PMID 35471084 Citation Status PubMed-not-MEDLINE |
---|
doi: |
10.1101/2020.11.09.375139 |
---|
funding: |
|
---|---|
Förderinstitution / Projekttitel: |
|
PPN (Katalog-ID): |
NLM317674382 |
---|
LEADER | 01000naa a22002652 4500 | ||
---|---|---|---|
001 | NLM317674382 | ||
003 | DE-627 | ||
005 | 20231225163747.0 | ||
007 | cr uuu---uuuuu | ||
008 | 231225s2020 xx |||||o 00| ||eng c | ||
024 | 7 | |a 10.1101/2020.11.09.375139 |2 doi | |
028 | 5 | 2 | |a pubmed24n1058.xml |
035 | |a (DE-627)NLM317674382 | ||
035 | |a (NLM)33200129 | ||
035 | |a (PII)2020.11.09.375139 | ||
040 | |a DE-627 |b ger |c DE-627 |e rakwb | ||
041 | |a eng | ||
100 | 1 | |a Moghadasi, Seyad Arad |e verfasserin |4 aut | |
245 | 1 | 0 | |a Gain-of-function assay for SARS-CoV-2 M pro inhibition in living cells |
264 | 1 | |c 2020 | |
336 | |a Text |b txt |2 rdacontent | ||
337 | |a ƒaComputermedien |b c |2 rdamedia | ||
338 | |a ƒa Online-Ressource |b cr |2 rdacarrier | ||
500 | |a Date Revised 03.05.2023 | ||
500 | |a published: Electronic | ||
500 | |a UpdateIn: mBio. 2022 Jun 28;13(3):e0078422. - PMID 35471084 | ||
500 | |a Citation Status PubMed-not-MEDLINE | ||
520 | |a The main protease, M pro , of SARS-CoV-2 is required to cleave the viral polyprotein into precise functional units for virus replication and pathogenesis. Here we demonstrate a quantitative reporter for M pro function in living cells, in which protease inhibition by genetic or chemical methods results in strong eGFP fluorescence. This robust gain-of-function system readily distinguishes between inhibitor potencies and can be scaled-up to high-throughput platforms for drug testing | ||
650 | 4 | |a Preprint | |
700 | 1 | |a Becker, Jordan T |e verfasserin |4 aut | |
700 | 1 | |a Belica, Christopher |e verfasserin |4 aut | |
700 | 1 | |a Wick, Chloe |e verfasserin |4 aut | |
700 | 1 | |a Brown, William L |e verfasserin |4 aut | |
700 | 1 | |a Harris, Reuben S |e verfasserin |4 aut | |
773 | 0 | 8 | |i Enthalten in |t bioRxiv : the preprint server for biology |d 2020 |g (2020) vom: 09. Nov. |w (DE-627)NLM31090014X |7 nnns |
773 | 1 | 8 | |g year:2020 |g day:09 |g month:11 |
856 | 4 | 0 | |u http://dx.doi.org/10.1101/2020.11.09.375139 |3 Volltext |
912 | |a GBV_USEFLAG_A | ||
912 | |a GBV_NLM | ||
951 | |a AR | ||
952 | |j 2020 |b 09 |c 11 |