School of Molecular and Cellular Biology, University of Leeds, LS2 9JT Leeds, United Kingdom.
Dipartimento di Fisica e Astronomia, Università di Bologna, 40127 Bologna, Italy.
J Am Soc Mass Spectrom. 2022 May 4;33(5):813-822. doi: 10.1021/jasms.2c00005. Epub 2022 Apr 6.
Experimental measurement of time-dependent spontaneous exchange of amide protons with deuterium of the solvent provides information on the structure and dynamical structural variation in proteins. Two experimental techniques are used to probe the exchange: NMR, which relies on different magnetic properties of hydrogen and deuterium, and MS, which exploits the change in mass due to deuteration. NMR provides residue-specific information, that is, the rate of exchange or, analogously, the protection factor (i.e., the unitless ratio between the rate of exchange for a completely unstructured state and the observed rate). MS provides information that is specific to peptides obtained by proteolytic digestion. The spatial resolution of HDX-MS measurements depends on the proteolytic pattern of the protein, the fragmentation method used, and the overlap between peptides. Different computational approaches have been proposed to extract residue-specific information from peptide-level HDX-MS measurements. Here, we demonstrate the advantages of a method recently proposed that exploits self-consistency and classifies the possible sets of protection factors into a finite number of alternative solutions compatible with experimental data. The degeneracy of the solutions can be reduced (or completely removed) by exploiting the additional information encoded in the shape of the isotopic envelopes. We show how sparse and noisy MS data can provide high-resolution protection factors that correlate with NMR measurements probing the same protein under the same conditions.
实验测量溶剂中酰胺质子与氘的随时间变化的自发交换,为蛋白质的结构和动态结构变化提供信息。有两种实验技术可用于探测交换:NMR,它依赖于氢和氘的不同磁性质;MS,它利用氘化引起的质量变化。NMR 提供残基特异性信息,即交换速率或类似地,保护因子(即无单位的完全无规状态的交换速率与观察到的交换速率之比)。MS 提供通过蛋白水解消化获得的肽的特异性信息。HDX-MS 测量的空间分辨率取决于蛋白质的蛋白水解模式、使用的片段化方法以及肽之间的重叠。已经提出了不同的计算方法来从肽水平的 HDX-MS 测量中提取残基特异性信息。在这里,我们展示了最近提出的一种方法的优势,该方法利用自洽性,并将可能的保护因子集分类为与实验数据兼容的有限数量的替代解。通过利用同位素包络形状中编码的附加信息,可以减少(或完全消除)解的简并性。我们展示了如何从稀疏且嘈杂的 MS 数据中获取与在相同条件下探测同一蛋白质的 NMR 测量相关的高分辨率保护因子。