Renneboog-Squilbin C
Int J Pept Protein Res. 1980 Jan;15(1):41-53. doi: 10.1111/j.1399-3011.1980.tb02548.x.
The insulins of pig, ox, horse and goat differ only by the cyclic A6-A11 peptide which is thought to be an antigenic determinant of the molecule. The structure of the four peptides is investigated by conformational energy calculations in order to verify whether a common backbone conformation can be found for all four species, the antigenic difference being consequently due only to the difference in the side chains exposed to the solvent, or whether each sequence gives rise to a preferential backbone conformation, which would lead to the conclusion that the antigenic difference is conveyed by a more pronounced difference in the molecular structure. From the results of the study on the isolated peptides, it appears that an energetically favourable backbone conformation common to all four species can be found. This conformation is compared with the structure deduced from the X-ray diffraction data available for pig insulin.
猪、牛、马和山羊的胰岛素仅在环A6 - A11肽段有所不同,该肽段被认为是该分子的一个抗原决定簇。通过构象能量计算研究这四种肽段的结构,以验证是否能为所有四个物种找到共同的主链构象,抗原差异因此仅归因于暴露于溶剂中的侧链差异,或者每个序列是否会产生优先的主链构象,这将导致得出抗原差异是由分子结构中更显著的差异所传递的结论。从对分离肽段的研究结果来看,似乎可以找到所有四个物种共有的能量有利的主链构象。将此构象与从猪胰岛素的X射线衍射数据推导得出的结构进行比较。