Pardo L, Ballesteros J A, Osman R, Weinstein H
Department of Physiology and Biophysics, Mount Sinai School of Medicine, New York, NY 10029-6574.
Proc Natl Acad Sci U S A. 1992 May 1;89(9):4009-12. doi: 10.1073/pnas.89.9.4009.
The molecular architecture of bacteriorhodopsin (BR) is commonly regarded as a structural template for the three-dimensional structure of membrane receptors that are functionally coupled to guanine nucleotide-binding regulatory proteins (GPCR). More recently, specific molecular models of such GPCR were constructed on the basis of the functional and structural relation of rhodopsin to BR as well as the sequence homology between rhodopsin and the GPCR. Such models of GPCR leave unresolved the difficulty caused by the apparent lack of any significant degree of sequence homology between the seven transmembrane helices (TMH) of BR and the portions in the sequence of the various GPCR that are considered to constitute their transmembrane domains. Evolutionary arguments offered in favor of the structural relation between BR and the opsins, and hence the GPCR, prompted our investigation of the possibility that the sequence homology, including any similarity in the distribution of kink-inducing proline residues among the helices, might have been obscured by the assumption that the TMH maintained their sequential order from BR in the evolution of the mammalian proteins. With a definition of the TMH in the neurotransmitter GPCR guided by hydropathicity predictions, and additional criteria used to define the span of each helix, optimal alignment of each pair of sequences was determined with no gaps allowed in the matching. The resulting alignment proposed here reveals considerable homology between the TMH in BR and those in GPCR, if the sequential order of the helices is ignored. These findings suggest the possibility that exon shuffling could have occurred in the proposed evolution of the GPCR gene from BR and point to a modification of the BR template to account for the correct packing of the helices in the tertiary structures of GPCR. These findings could guide the construction of three-dimensional models of the neurotransmitter GPCR on the basis of specific interhelical interactions observed in BR.
细菌视紫红质(BR)的分子结构通常被视为与鸟嘌呤核苷酸结合调节蛋白(GPCR)功能偶联的膜受体三维结构的结构模板。最近,基于视紫红质与BR的功能和结构关系以及视紫红质与GPCR之间的序列同源性,构建了此类GPCR的特定分子模型。此类GPCR模型尚未解决由BR的七个跨膜螺旋(TMH)与各种GPCR序列中被认为构成其跨膜结构域的部分之间明显缺乏任何显著程度的序列同源性所导致的难题。支持BR与视蛋白以及因此与GPCR之间结构关系的进化观点促使我们研究这样一种可能性,即包括螺旋中诱导扭结的脯氨酸残基分布的任何相似性在内的序列同源性,可能已被哺乳动物蛋白质进化过程中TMH从BR保持其顺序的假设所掩盖。在亲水性预测的指导下定义神经递质GPCR中的TMH,并使用额外标准定义每个螺旋的跨度,在匹配中不允许有间隙的情况下确定每对序列的最佳比对。此处提出的比对结果表明,如果忽略螺旋的顺序,BR中的TMH与GPCR中的TMH之间存在相当大的同源性。这些发现表明在GPCR基因从BR的进化过程中可能发生了外显子重排,并指出对BR模板进行修改以解释GPCR三级结构中螺旋的正确堆积。这些发现可以指导基于BR中观察到的特定螺旋间相互作用构建神经递质GPCR的三维模型。