Department of Chemistry , University of Texas at Austin , Austin , Texas 78712 , United States.
Epigenetics Institute, Department of Biochemistry and Biophysics, Perelman School of Medicine , University of Pennsylvania , Philadelphia , Pennsylvania 19104 , United States.
Anal Chem. 2018 Sep 4;90(17):10425-10433. doi: 10.1021/acs.analchem.8b02320. Epub 2018 Aug 16.
The ability to map combinatorial patterns of post-translational modifications (PTMs) of proteins remains challenging for traditional bottom-up mass spectrometry workflows. There are also hurdles associated with top-down approaches related to limited data analysis options for heavily modified proteoforms. These shortcomings have accelerated interest in middle-down MS methods that focus on analysis of large peptides generated by specific proteases in conjunction with validated bioinformatics strategies to allow quantification of isomeric histoforms. Mapping multiple PTMs simultaneously requires the ability to obtain high sequence coverage to allow confident localization of the modifications, and 193 nm ultraviolet photodissociation (UVPD) has been shown to cause extensive fragmentation for large peptides and proteins. Histones are an ideal system to test the ability of UVPD to characterize multiple modifications, as the combinations of PTMs are the underpinning of the biological significance of histones and at the same time create an imposing challenge for characterization. The present study focuses on applying 193 nm UVPD to the identification and localization of PTMs on histones by UVPD and comparison to a popular alternative, electron-transfer dissociation (ETD), via a high-throughput middle-down LC/MS/MS strategy. Histone Coder and IsoScale, bioinformatics tools for verification of PTM assignments and quantification of histone peptides, were adapted for UVPD data and applied in the present study. In total, over 300 modified forms were identified, and the distributions of PTMs were quantified between UVPD and ETD. Significant differences in patterns of PTMs were found for histones from HeLa cells prior to and after treatment with a deacetylase inhibitor. Additional fragment ion types generated by UVPD proved essential for extensive characterization of the most heavily modified forms (>5 PTMs).
蛋白质翻译后修饰(PTMs)的组合模式作图能力仍然是传统的自上而下质谱工作流程面临的挑战。与大量修饰的蛋白形式相关的数据分析选项有限,这也给自上而下的方法带来了障碍。这些缺点加速了对中向 MS 方法的兴趣,这些方法侧重于与验证的生物信息学策略相结合,分析特定蛋白酶产生的大肽,以允许对同型结构进行定量。同时分析多个 PTM 需要能够获得高序列覆盖率以允许对修饰进行有信心的定位,并且已经证明 193nm 紫外线光解(UVPD)会导致大肽和蛋白质的广泛碎裂。组蛋白是测试 UVPD 对多种修饰进行特征描述能力的理想系统,因为 PTM 的组合是组蛋白生物学意义的基础,同时也为特征描述带来了巨大的挑战。本研究重点应用 193nmUVPD 通过高通量中向 LC/MS/MS 策略,对组蛋白上的 PTM 进行鉴定和定位,并与流行的替代方法电子转移解离(ETD)进行比较。本研究中适应了组蛋白编码和 IsoScale 等生物信息学工具,用于验证 PTM 分配和定量组蛋白肽。总共鉴定了 300 多种修饰形式,并在 UVPD 和 ETD 之间量化了 PTM 的分布。在用去乙酰化酶抑制剂处理 HeLa 细胞前后,组蛋白中的 PTM 模式存在显著差异。UVPD 产生的额外片段离子类型对于广泛表征修饰程度最高的形式(>5 种 PTM)至关重要。