Exploratory Research Center on Life and Living Systems (ExCELLS) and Institute for Molecular Science (IMS), National Institutes of Natural Sciences, Myodaiji, Okazaki, Aichi, Japan.
Department of Functional Molecular Science, School of Physical Sciences, SOKENDAI (the Graduate University for Advanced Studies), Myodaiji, Okazaki, Aichi, Japan.
Protein Sci. 2023 Mar;32(3):e4569. doi: 10.1002/pro.4569.
The characterization of residual structures persistent in unfolded proteins is an important issue in studies of protein folding, because the residual structures present, if any, may form a folding initiation site and guide the subsequent folding reactions. Here, we studied the residual structures of the isolated B domain (BDPA) of staphylococcal protein A in 6 M guanidinium chloride. BDPA is a small three-helix-bundle protein, and until recently its folding/unfolding reaction has been treated as a simple two-state process between the native and the fully unfolded states. We employed a dimethylsulfoxide (DMSO)-quenched hydrogen/deuterium (H/D)-exchange 2D NMR techniques with the use of spin desalting columns, which allowed us to investigate the H/D-exchange behavior of individually identified peptide amide (NH) protons. We obtained H/D-exchange protection factors of the 21 NH protons that form an α-helical hydrogen bond in the native structure, and the majority of these NH protons were significantly protected with a protection factor of 2.0-5.2 in 6 M guanidinium chloride, strongly suggesting that these weakly protected NH protons form much stronger hydrogen bonds under native folding conditions. The results can be used to deduce the structure of an early folding intermediate, when such an intermediate is shown by other methods. Among three native helical regions, the third helix in the C-terminal side was highly protected and stabilized by side-chain salt bridges, probably acting as the folding initiation site of BDPA. The present results are discussed in relation to previous experimental and computational findings on the folding mechanisms of BDPA.
研究未折叠蛋白质中残留结构的特征是蛋白质折叠研究中的一个重要问题,因为如果存在残留结构,它们可能形成折叠起始位点,并指导随后的折叠反应。在这里,我们研究了葡萄球菌蛋白 A 的分离 B 结构域(BDPA)在 6 M 盐酸胍中的残留结构。BDPA 是一个小的三螺旋束蛋白,直到最近,其折叠/去折叠反应一直被视为天然状态和完全去折叠状态之间的简单两态过程。我们使用二甲基亚砜(DMSO)猝灭的氢/氘(H/D)交换二维 NMR 技术,使用自旋脱盐柱,这使我们能够研究单独鉴定的肽酰胺(NH)质子的 H/D 交换行为。我们获得了 21 个 NH 质子的 H/D 交换保护因子,这些质子在天然结构中形成α-螺旋氢键,其中大多数 NH 质子在 6 M 盐酸胍中具有 2.0-5.2 的保护因子,强烈表明这些弱保护 NH 质子在天然折叠条件下形成更强的氢键。这些结果可用于推断早期折叠中间物的结构,当其他方法显示存在这样的中间物时。在三个天然螺旋区域中,C 末端的第三个螺旋通过侧链盐桥得到高度保护和稳定,可能作为 BDPA 的折叠起始位点。目前的结果与之前关于 BDPA 折叠机制的实验和计算结果进行了讨论。