TY - JOUR
T1 - Characteristics Affecting Expression and Solubilization of Yeast Membrane Proteins
AU - White, Michael A.
AU - Clark, Kathleen M.
AU - Grayhack, Elizabeth J.
AU - Dumont, Mark E.
N1 - Funding Information:
We thank Drs Gregory Tombline and Zulfiqar Ahmad for assistance in setting up the ATPase assays. This work was supported in part by NIH grant HG02311 to Eric Phizicky and a sybcontract to M.E.D. of grant U54 GM074899 to the Center for High Throughput Stuctural Biology, P.I. George DeTitta.
PY - 2007/1/19
Y1 - 2007/1/19
N2 - Biochemical and structural analysis of membrane proteins often critically depends on the ability to overexpress and solubilize them. To identify properties of eukaryotic membrane proteins that may be predictive of successful overexpression, we analyzed expression levels of the genomic complement of over 1000 predicted membrane proteins in a recently completed Saccharomyces cerevisiae protein expression library. We detected statistically significant positive and negative correlations between high membrane protein expression and protein properties such as size, overall hydrophobicity, number of transmembrane helices, and amino acid composition of transmembrane segments. Although expression levels of membrane and soluble proteins exhibited similar negative correlations with overall hydrophobicity, high-level membrane protein expression was positively correlated with the hydrophobicity of predicted transmembrane segments. To further characterize yeast membrane proteins as potential targets for structure determination, we tested the solubility of 122 of the highest expressed yeast membrane proteins in six commonly used detergents. Almost all the proteins tested could be solubilized using a small number of detergents. Solubility in some detergents depended on protein size, number of transmembrane segments, and hydrophobicity of predicted transmembrane segments. These results suggest that bioinformatic approaches may be capable of identifying membrane proteins that are most amenable to overexpression and detergent solubilization for structural and biochemical analyses. Bioinformatic approaches could also be used in the redesign of proteins that are not intrinsically well-adapted to such studies.
AB - Biochemical and structural analysis of membrane proteins often critically depends on the ability to overexpress and solubilize them. To identify properties of eukaryotic membrane proteins that may be predictive of successful overexpression, we analyzed expression levels of the genomic complement of over 1000 predicted membrane proteins in a recently completed Saccharomyces cerevisiae protein expression library. We detected statistically significant positive and negative correlations between high membrane protein expression and protein properties such as size, overall hydrophobicity, number of transmembrane helices, and amino acid composition of transmembrane segments. Although expression levels of membrane and soluble proteins exhibited similar negative correlations with overall hydrophobicity, high-level membrane protein expression was positively correlated with the hydrophobicity of predicted transmembrane segments. To further characterize yeast membrane proteins as potential targets for structure determination, we tested the solubility of 122 of the highest expressed yeast membrane proteins in six commonly used detergents. Almost all the proteins tested could be solubilized using a small number of detergents. Solubility in some detergents depended on protein size, number of transmembrane segments, and hydrophobicity of predicted transmembrane segments. These results suggest that bioinformatic approaches may be capable of identifying membrane proteins that are most amenable to overexpression and detergent solubilization for structural and biochemical analyses. Bioinformatic approaches could also be used in the redesign of proteins that are not intrinsically well-adapted to such studies.
KW - detergents
KW - membrane proteins
KW - protein overexpression
KW - structural genomics
KW - yeast
UR - http://www.scopus.com/inward/record.url?scp=33845629883&partnerID=8YFLogxK
U2 - 10.1016/j.jmb.2006.10.004
DO - 10.1016/j.jmb.2006.10.004
M3 - Article
C2 - 17078969
AN - SCOPUS:33845629883
SN - 0022-2836
VL - 365
SP - 621
EP - 636
JO - Journal of Molecular Biology
JF - Journal of Molecular Biology
IS - 3
ER -