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Cell-free synthesis and reconstitution of Bax in nanodiscs: Comparison between wild-type Bax and a constitutively active mutant.

Authors :
Rouchidane Eyitayo, Akandé
Giraud, Marie-France
Daury, Laetitia
Lambert, Olivier
Gonzalez, Cécile
Manon, Stéphen
Source :
BBA: Biomembranes. Jan2023, Vol. 1865 Issue 1, pN.PAG-N.PAG. 1p.
Publication Year :
2023

Abstract

Bax is a major player in the mitochondrial pathway of apoptosis, by making the Outer Mitochondrial Membrane (OMM) permeable to various apoptogenic factors, including cytochrome c. In order to get further insight into the structure and function of Bax when it is inserted in the OMM, we attempted to reconstitute Bax in nanodiscs. Cell-free protein synthesis in the presence of nanodiscs did not yield Bax-containing nanodiscs, but it provided a simple way to purify full-length Bax without any tag. Purified wild-type Bax (BaxWT) and a constitutively active mutant (BaxP168A) displayed biochemical properties that were in line with previous characterizations following their expression in yeast and human cells followed by their reconstitution into liposomes. Both Bax variants were then reconstituted in nanodiscs. Size exclusion chromatography, dynamic light scattering and transmission electron microscopy showed that nanodiscs formed with BaxP168A were larger than nanodiscs formed with BaxWT. This was consistent with the hypothesis that BaxP168A was reconstituted in nanodiscs as an active oligomer. [Display omitted] • Cell-free synthesis of Bax in the presence of nanodiscs did not allow a direct insertion of the protein • However, Bax could be adequatly purified for biochemical studies • Both BaxWT and the active mutant BaxP168A could be further reconstituted into nanodiscs by co-formation • Nanodiscs containing BaxP168A were larger, suggesting that it was reconstituted as an oligomer [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00052736
Volume :
1865
Issue :
1
Database :
Academic Search Index
Journal :
BBA: Biomembranes
Publication Type :
Academic Journal
Accession number :
160166566
Full Text :
https://doi.org/10.1016/j.bbamem.2022.184075