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Improved Protein Hydrogen/Deuterium Exchange Mass Spectrometry Platform with Fully Automated Data Processing

机译:具有全自动数据处理功能的改进的蛋白质氢/氘交换质谱平台

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摘要

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.
机译:蛋白质氢/氘交换(HDX),然后进行蛋白酶消化和质谱(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。在本文中,将介绍一种具有全自动数据处理功能的改进的HDX MS平台。该平台通过在HDX数据分析中引入两种类型的校正,大大减少了测量中的系统误差和随机误差。首先,引入具有快速HDX速率的短肽混合物作为内标,以调整每次运行之间反向交换程度的变化。其次,将设计的具有固有HDX速率慢的独特肽(PPPI)用作另一种内标,以反映在比较不同溶液条件下的蛋白质构象时蛋白质固有HDX速率的可能差异。 HDX数据处理通过全面的HDX模型实现,以模拟氘标记和反向交换过程。 HDX模型已在内部开发的软件MassAnalyzer中实现,并且可以对整个蛋白质HDX MS数据集进行完全无人值守的分析,从离子检测和肽鉴定到最终处理的HDX输出(通常在1天之内)。自动化数据处理的最终输出是每个主链酰胺氢最可能的保护因子的集合(或平均值)。 HDX MS平台的实用性通过增加胍的浓度探索单克隆抗体的构象转变来证明。

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