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改进的蛋白质氢/氘交换质谱平台,具有全自动数据处理功能。

Improved protein hydrogen/deuterium exchange mass spectrometry platform with fully automated data processing.

机构信息

Process and Product Development, Amgen Inc., One Amgen Center Drive, Thousand Oaks, California 91320, United States.

出版信息

Anal Chem. 2012 Jun 5;84(11):4942-9. doi: 10.1021/ac300535r. Epub 2012 May 15.

Abstract

Protein hydrogen/deuterium exchange (HDX) followed by protease digestion and mass spectrometric (MS) analysis is accepted as a standard method for studying protein conformation and conformational dynamics. In this article, an improved HDX MS platform with fully automated data processing is described. The platform significantly reduces systematic and random errors in the measurement by introducing two types of corrections in HDX data analysis. First, a mixture of short peptides with fast HDX rates is introduced as internal standards to adjust the variations in the extent of back exchange from run to run. Second, a designed unique peptide (PPPI) with slow intrinsic HDX rate is employed as another internal standard to reflect the possible differences in protein intrinsic HDX rates when protein conformations at different solution conditions are compared. HDX data processing is achieved with a comprehensive HDX model to simulate the deuterium labeling and back exchange process. The HDX model is implemented into the in-house developed software MassAnalyzer and enables fully unattended analysis of the entire protein HDX MS data set starting from ion detection and peptide identification to final processed HDX output, typically within 1 day. The final output of the automated data processing is a set (or the average) of the most possible protection factors for each backbone amide hydrogen. The utility of the HDX MS platform is demonstrated by exploring the conformational transition of a monoclonal antibody by increasing concentrations of guanidine.

摘要

蛋白质氢/氘交换(HDX)结合蛋白酶消化和质谱(MS)分析被认为是研究蛋白质构象和构象动力学的标准方法。本文描述了一种具有全自动数据处理功能的改进型 HDX MS 平台。该平台通过在 HDX 数据分析中引入两种校正方法,显著降低了测量中的系统和随机误差。首先,引入具有快速 HDX 速率的短肽混合物作为内标,以调整不同运行之间的反向交换程度的变化。其次,使用设计的具有缓慢固有 HDX 速率的独特肽(PPPI)作为另一个内标,以反映比较不同溶液条件下蛋白质构象时蛋白质固有 HDX 速率的可能差异。HDX 数据处理是通过综合的 HDX 模型来实现的,该模型模拟氘标记和反向交换过程。HDX 模型被实现到内部开发的 MassAnalyzer 软件中,能够从离子检测和肽鉴定开始,对整个蛋白质 HDX MS 数据集进行全自动分析,最终处理后的 HDX 输出通常在 1 天内完成。自动化数据处理的最终输出是每个骨架酰胺氢的最可能保护因子的集合(或平均值)。通过增加胍盐浓度来探索单克隆抗体的构象转变,证明了 HDX MS 平台的实用性。

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