Puchała Weronika, Kistowski Michał, Zhukova Liliya, Burdukiewicz Michał, Dadlez Michał
Institute of Biochemistry and Biophysics, Polish Academy of Sciences, Warsaw 02-106, Poland.
Clinical Research Centre, Medical University of Białystok, Białystok, 15-369, Poland.
J Proteome Res. 2025 Apr 4;24(4):1688-1700. doi: 10.1021/acs.jproteome.4c00700. Epub 2025 Mar 19.
Hydrogen-deuterium exchange monitored by mass spectrometry (HDX-MS) is a well-established and powerful technique used to study protein dynamics and stability by capturing local and global unfolding events in protein structures. However, in this technique, obtaining region-specific information requires proteolytic digestion that breaks the protein into peptide fragments, causing the HDX data to reflect averages over these fragments rather than individual amino acids. We propose a new computational method that provides deuterium uptake kinetic parameters with high resolution, considering deuterium uptake trajectories of superimposed peptides. Our algorithm, HRaDeX, is available as a web server and an R package capable of processing data from single-state and comparative HDX-MS studies. Utilizing eight benchmark data sets, we demonstrate that HRaDeX reaches an average root-mean-square error of 7.15% in the reconstitution of experimental normalized deuterium uptake curves.
通过质谱监测的氢-氘交换(HDX-MS)是一种成熟且强大的技术,用于通过捕捉蛋白质结构中的局部和整体去折叠事件来研究蛋白质动力学和稳定性。然而,在该技术中,获取区域特异性信息需要进行蛋白水解消化,将蛋白质分解成肽片段,这使得HDX数据反映的是这些片段的平均值,而非单个氨基酸的情况。我们提出了一种新的计算方法,该方法考虑叠加肽的氘摄取轨迹,能够高分辨率地提供氘摄取动力学参数。我们的算法HRaDeX可作为网络服务器和R包使用,能够处理来自单状态和比较HDX-MS研究的数据。利用八个基准数据集,我们证明HRaDeX在重构实验归一化氘摄取曲线时的平均均方根误差达到7.15%。