%0 Journal Article %1 Li2015TSPOCholesterolBinding %A Li, Fei %A Liu, Jian %A Valls, Lance %A Hiser, Carrie %A Ferguson-Miller, Shelagh %D 2015 %J Biochemistry %K TSPO cholesterol ligand-binding %N 7 %P 1441-1443 %R 10.1021/bi5015453 %T Identification of a Key Cholesterol Binding Enhancement Motif in Translocator Protein 18 kDa %U http://dx.doi.org/10.1021/bi5015453 %V 54 %X Translocator protein 18 kDa (TSPO) in the mitochondrial outer membrane has been implicated in cholesterol transport regulating steroidogenesis. A human single polymorphism associated with anxiety disorders (A147T) and reduced pregnenolone production is adjacent to TSPO’s cholesterol binding motif. In a mutant mimicking this polymorphism, we observe a lower level of binding of cholesterol. Further, three residues preceding A147 are more hydrophilic in a bacterial TSPO that has an affinity for cholesterol 1000-fold lower than that of the human form. Converting these residues to the human form in the bacterial homologue strikingly increases the affinity for cholesterol. An important role for this extended motif is further supported by covariance analysis.

@article{Li2015TSPOCholesterolBinding, abstract = { Translocator protein 18 kDa (TSPO) in the mitochondrial outer membrane has been implicated in cholesterol transport regulating steroidogenesis. A human single polymorphism associated with anxiety disorders (A147T) and reduced pregnenolone production is adjacent to TSPO’s cholesterol binding motif. In a mutant mimicking this polymorphism, we observe a lower level of binding of cholesterol. Further, three residues preceding A147 are more hydrophilic in a bacterial TSPO that has an affinity for cholesterol 1000-fold lower than that of the human form. Converting these residues to the human form in the bacterial homologue strikingly increases the affinity for cholesterol. An important role for this extended motif is further supported by covariance analysis. }, added-at = {2016-01-12T16:07:27.000+0100}, author = {Li, Fei and Liu, Jian and Valls, Lance and Hiser, Carrie and Ferguson-Miller, Shelagh}, biburl = {https://www.bibsonomy.org/bibtex/2d15436b8ffcc394eed2e75c1237d9837/salotz}, description = {Identification of a Key Cholesterol Binding Enhancement Motif in Translocator Protein 18 kDa - Biochemistry (ACS Publications)}, doi = {10.1021/bi5015453}, eprint = {http://dx.doi.org/10.1021/bi5015453}, interhash = {eb3b3d2e514891a5e82ad997865f3d73}, intrahash = {d15436b8ffcc394eed2e75c1237d9837}, journal = {Biochemistry}, keywords = {TSPO cholesterol ligand-binding}, note = {PMID: 25635829}, number = 7, pages = {1441-1443}, timestamp = {2016-01-12T19:15:51.000+0100}, title = {Identification of a Key Cholesterol Binding Enhancement Motif in Translocator Protein 18 kDa}, url = {http://dx.doi.org/10.1021/bi5015453 }, volume = 54, year = 2015 }