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An Approach to Heterologous Expression of Membrane Proteins. The Case of Bacteriorhodopsin
- Source :
- PLoS one 10(6), e0128390-(2015). doi:10.1371/journal.pone.0128390, 'PloS One ', vol: 10, pages: e0128390-1-e0128390-16 (2015), PLoS ONE, Vol 10, Iss 6, p e0128390 (2015), PLOS ONE 10(6), e0128390 (2015). doi:10.1371/journal.pone.0128390, PLoS ONE, PLoS ONE, 2015, 10 (6), pp.e0128390, PLoS ONE, Public Library of Science, 2015, 10 (6), pp.e0128390
- Publication Year :
- 2015
- Publisher :
- PLoS, 2015.
-
Abstract
- International audience; Heterologous overexpression of functional membrane proteins is a major bottleneck of structural biology. Bacteriorhodopsin from Halobium salinarum (bR) is a striking example of the difficulties in membrane protein overexpression. We suggest a general approach with a finite number of steps which allows one to localize the underlying problem of poor expression of a membrane protein using bR as an example. Our approach is based on constructing chimeric proteins comprising parts of a protein of interest and complementary parts of a homologous protein demonstrating advantageous expression. This complementary protein approach allowed us to increase bR expression by two orders of magnitude through the introduction of two silent mutations into bR coding DNA. For the first time the high quality crystals of bR expressed in E. Coli were obtained using the produced protein. The crystals obtained with in meso nanovolume crystallization diffracted to 1.67 Å.
- Subjects :
- Halobacterium salinarum
[SDV.BBM.BS]Life Sciences [q-bio]/Biochemistry, Molecular Biology/Structural Biology [q-bio.BM]
[SDV.BBM.BS] Life Sciences [q-bio]/Biochemistry, Molecular Biology/Structural Biology [q-bio.BM]
Molecular Sequence Data
lcsh:R
lcsh:Medicine
Crystallography, X-Ray
Recombinant Proteins
Protein Structure, Tertiary
Bacteriorhodopsins
Escherichia coli
Mutagenesis, Site-Directed
Nucleic Acid Conformation
lcsh:Q
Amino Acid Sequence
RNA, Messenger
ddc:500
lcsh:Science
Sequence Alignment
Research Article
Subjects
Details
- Language :
- English
- ISSN :
- 19326203
- Database :
- OpenAIRE
- Journal :
- PLoS one 10(6), e0128390-(2015). doi:10.1371/journal.pone.0128390, 'PloS One ', vol: 10, pages: e0128390-1-e0128390-16 (2015), PLoS ONE, Vol 10, Iss 6, p e0128390 (2015), PLOS ONE 10(6), e0128390 (2015). doi:10.1371/journal.pone.0128390, PLoS ONE, PLoS ONE, 2015, 10 (6), pp.e0128390, PLoS ONE, Public Library of Science, 2015, 10 (6), pp.e0128390
- Accession number :
- edsair.pmid.dedup....2824be7720486145737cc4413ca8caae
- Full Text :
- https://doi.org/10.1371/journal.pone.0128390