Aquila H, Link T A, Klingenberg M
EMBO J. 1985 Sep;4(9):2369-76. doi: 10.1002/j.1460-2075.1985.tb03941.x.
We report here, for the first time, the primary structure of uncoupling protein as established by amino acid sequencing. Like the ADP/ATP carrier, this protein has a tripartite structure comprising three similar sequences of approximately 100 residues each. These six 'repeats' exhibit striking conservation of several residues, in particular glycine and proline, at possible structurally strategic positions. Although the two proteins differ strongly in their amino acid composition, their sequences are distantly homologous. Three membrane-spanning alpha-helices can be deduced from hydropathy plots. A modified plot accounting for amphiphilic helices indicates 5-6 such alpha-segments. In addition an amphiphilic beta-strand of membrane-spanning length can be discerned. The tripartite sequence structure is also distinctly reflected in the hydropathy distribution. Based on the membrane disposition of the segments of the ADP/ATP carrier, a model for the transmembrane folding path of the polypeptide chain of the uncoupling protein is proposed.
我们在此首次报告通过氨基酸测序确定的解偶联蛋白的一级结构。与ADP/ATP载体一样,该蛋白具有三重结构,由三个各约含100个残基的相似序列组成。这六个“重复序列”在可能具有结构战略意义的位置上,几个残基,特别是甘氨酸和脯氨酸,表现出显著的保守性。尽管这两种蛋白的氨基酸组成差异很大,但它们的序列具有远缘同源性。从亲水性图谱可推断出三个跨膜α螺旋。一个考虑了两亲性螺旋的修正图谱显示有5至6个这样的α片段。此外,还可识别出一个具有跨膜长度的两亲性β链。三重序列结构在亲水性分布中也有明显体现。基于ADP/ATP载体各片段的膜定位,提出了解偶联蛋白多肽链跨膜折叠路径的模型。