Li Fei, Liu Jian, Valls Lance, Hiser Carrie, Ferguson-Miller Shelagh
Department of Biochemistry and Molecular Biology, Michigan State University , East Lansing, Michigan 48824, United States.
Biochemistry. 2015 Feb 24;54(7):1441-3. doi: 10.1021/bi5015453. Epub 2015 Feb 10.
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.
线粒体外膜中的18 kDa转位蛋白(TSPO)与胆固醇转运相关,参与调节类固醇生成。一种与焦虑症相关的人类单核苷酸多态性(A147T)以及孕烯醇酮生成减少与TSPO的胆固醇结合基序相邻。在模拟这种多态性的突变体中,我们观察到胆固醇的结合水平较低。此外,在一种对胆固醇的亲和力比人类形式低1000倍的细菌TSPO中,A147之前的三个残基更具亲水性。在细菌同源物中将这些残基转换为人类形式会显著增加对胆固醇的亲和力。共变分析进一步支持了这个扩展基序的重要作用。