TY - JOUR
T1 - A comprehensive library of fluorescent constructs of SARS-CoV-2 proteins and their initial characterisation in different cell types
AU - Miserey-Lenkei, Stéphanie
AU - Trajkovic, Katarina
AU - D'Ambrosio, Juan Martín
AU - Patel, Amanda J.
AU - Čopič, Alenka
AU - Mathur, Pallavi
AU - Schauer, Kristine
AU - Goud, Bruno
AU - Albanèse, Véronique
AU - Gautier, Romain
AU - Subra, Melody
AU - Kovacs, David
AU - Barelli, Hélène
AU - Antonny, Bruno
N1 - Publisher Copyright:
© 2021 Société Française des Microscopies and Société de Biologie Cellulaire de France. Published by John Wiley & Sons Ltd.
PY - 2021/7/1
Y1 - 2021/7/1
N2 - Background Information: Comprehensive libraries of plasmids for SARS-CoV-2 proteins with various tags (e.g., Strep, HA, Turbo) are now available. They enable the identification of numerous potential protein–protein interactions between the SARS-CoV-2 virus and host proteins. Results: We present here a large library of SARS CoV-2 protein constructs fused with green and red fluorescent proteins and their initial characterisation in various human cell lines including lung epithelial cell models (A549, BEAS-2B), as well as in budding yeast. The localisation of a few SARS-CoV-2 proteins matches their proposed interactions with host proteins. These include the localisation of Nsp13 to the centrosome, Orf3a to late endosomes and Orf9b to mitochondria. Conclusions and Significance: This library should facilitate further cellular investigations, notably by imaging techniques.
AB - Background Information: Comprehensive libraries of plasmids for SARS-CoV-2 proteins with various tags (e.g., Strep, HA, Turbo) are now available. They enable the identification of numerous potential protein–protein interactions between the SARS-CoV-2 virus and host proteins. Results: We present here a large library of SARS CoV-2 protein constructs fused with green and red fluorescent proteins and their initial characterisation in various human cell lines including lung epithelial cell models (A549, BEAS-2B), as well as in budding yeast. The localisation of a few SARS-CoV-2 proteins matches their proposed interactions with host proteins. These include the localisation of Nsp13 to the centrosome, Orf3a to late endosomes and Orf9b to mitochondria. Conclusions and Significance: This library should facilitate further cellular investigations, notably by imaging techniques.
KW - Intracellular compartmentalisation
KW - Light microscopy
KW - Membranes
KW - Molecular interactions
KW - Viruses
UR - http://www.scopus.com/inward/record.url?scp=85105370085&partnerID=8YFLogxK
U2 - 10.1111/boc.202000158
DO - 10.1111/boc.202000158
M3 - Article
C2 - 33666950
AN - SCOPUS:85105370085
SN - 0248-4900
VL - 113
SP - 311
EP - 328
JO - Biology of the Cell
JF - Biology of the Cell
IS - 7
ER -