Dyson H J, Merutka G, Waltho J P, Lerner R A, Wright P E
Department of Molecular Biology, Scripps Research Institute, La Jolla, CA 92037.
J Mol Biol. 1992 Aug 5;226(3):795-817. doi: 10.1016/0022-2836(92)90633-u.
In an attempt to delineate potential folding initiation sites for different protein structural motifs, we have synthesized series of peptides that span the entire length of the polypeptide chain of two proteins, and examined their conformational preferences in aqueous solution using proton nuclear magnetic resonance and circular dichroism spectroscopy. We describe here the behavior of peptides derived from a simple four-helix bundle protein, myohemerythrin. The peptides correspond to the sequences of the four long helices (the A, B, C and D helices), the N- and C-terminal loops and the connecting sequences between the helices. The peptides corresponding to the helices of the folded protein all exhibit preferences for helix-like conformations in solution. The conformational ensembles of the A- and D-helix peptides contain ordered helical forms, as shown by extensive series of medium-range nuclear Overhauser effect connectivities, while the B- and C-helix peptides exhibit conformational preferences for nascent helix. All four peptides adopt ordered helical conformations in mixtures of trifluoroethanol and water. The terminal and interconnecting loop peptides also appear to contain appreciable populations of conformers with backbone phi and psi angles in the alpha-region and include highly populated hydrophobic cluster and/or turn conformations in some cases. Trifluoroethanol is unable to drive these peptides towards helical conformations. Overall, the peptide fragments of myohemerythrin have a marked preference towards secondary structure formation in aqueous solution. In contrast, peptide fragments derived from the beta-sandwich protein plastocyanin are relatively devoid of secondary structure in aqueous solution (see accompanying paper). These results suggest that the two different protein structural motifs may require different propensities for formation of local elements of secondary structure to initiate folding, and that there is a prepartitioning of conformational space determined by the local amino acid sequence that is different for the helical and beta-sandwich structural motifs.
为了确定不同蛋白质结构基序的潜在折叠起始位点,我们合成了一系列跨越两种蛋白质多肽链全长的肽段,并利用质子核磁共振和圆二色光谱研究了它们在水溶液中的构象偏好。我们在此描述源自简单四螺旋束蛋白肌红蛋白的肽段的行为。这些肽段对应于四个长螺旋(A、B、C和D螺旋)、N端和C端环以及螺旋之间的连接序列的序列。对应于折叠蛋白螺旋的肽段在溶液中都表现出对螺旋样构象的偏好。A螺旋和D螺旋肽段的构象集合包含有序的螺旋形式,大量的中程核Overhauser效应连接性表明了这一点,而B螺旋和C螺旋肽段表现出对新生螺旋的构象偏好。所有四个肽段在三氟乙醇和水的混合物中都采用有序的螺旋构象。末端和连接环肽段似乎也包含相当数量的构象异构体,其主链φ和ψ角处于α区域,在某些情况下还包括高度密集的疏水簇和/或转角构象。三氟乙醇无法驱使这些肽段形成螺旋构象。总体而言,肌红蛋白的肽段片段在水溶液中对二级结构形成有明显偏好。相比之下,源自β折叠三明治蛋白质体蓝素的肽段片段在水溶液中相对缺乏二级结构(见随附论文)。这些结果表明,两种不同的蛋白质结构基序可能需要不同的二级结构局部元件形成倾向来启动折叠,并且存在由局部氨基酸序列决定的构象空间预分配,这对于螺旋和β折叠三明治结构基序是不同的。