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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 A
Giraud MF
Daury L
Lambert O
Gonzalez C
Manon S
Source :
Biochimica et biophysica acta. Biomembranes [Biochim Biophys Acta Biomembr] 2023 Jan 01; Vol. 1865 (1), pp. 184075. Date of Electronic Publication: 2022 Oct 20.
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.<br />Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.<br /> (Copyright © 2022. Published by Elsevier B.V.)

Details

Language :
English
ISSN :
1879-2642
Volume :
1865
Issue :
1
Database :
MEDLINE
Journal :
Biochimica et biophysica acta. Biomembranes
Publication Type :
Academic Journal
Accession number :
36273540
Full Text :
https://doi.org/10.1016/j.bbamem.2022.184075