4XXJ image
Deposition Date 2015-01-30
Release Date 2015-07-01
Last Version Date 2024-01-10
Entry Detail
PDB ID:
4XXJ
Keywords:
Title:
Crystal Structure of Escherichia coli-Expressed Halobacterium salinarum Bacteriorhodopsin in the Trimeric Form
Biological Source:
Source Organism(s):
Expression System(s):
Method Details:
Experimental Method:
Resolution:
1.90 Å
R-Value Free:
0.21
R-Value Work:
0.18
R-Value Observed:
0.18
Space Group:
C 1 2 1
Macromolecular Entities
Polymer Type:polypeptide(L)
Molecule:Bacteriorhodopsin
Gene (Uniprot):bop
Chain IDs:A, B, C
Chain Length:269
Number of Molecules:3
Biological Source:Halobacterium salinarum
Modified Residue
Compound ID Chain ID Parent Comp ID Details 2D Image
LYR A LYS modified residue
Primary Citation
An Approach to Heterologous Expression of Membrane Proteins. The Case of Bacteriorhodopsin.
PLoS ONE 10 e0128390 e0128390 (2015)
PMID: 26046789 DOI: 10.1371/journal.pone.0128390

Abstact

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.

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Primary Citation of related structures
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