蛋白质组学
表观遗传学
组蛋白
计算生物学
串联质谱法
等压标记
定量蛋白质组学
质谱法
翻译后修饰
色谱法
染色质
化学
生物
计算机科学
DNA
生物化学
酶
基因
蛋白质质谱法
作者
Zuo‐Fei Yuan,Simone Sidoli,Dylan M. Marchione,Johayra Simithy,Kevin A. Janssen,Mary R. Szurgot,Benjamin A. García
标识
DOI:10.1021/acs.jproteome.8b00133
摘要
Epigenetics has become a fundamental scientific discipline with various implications for biology and medicine. Epigenetic marks, mostly DNA methylation and histone post-translational modifications (PTMs), play important roles in chromatin structure and function. Accurate quantification of these marks is an ongoing challenge due to the variety of modifications and their wide dynamic range of abundance. Here we present EpiProfile 2.0, an extended version of our 2015 software (v1.0), for accurate quantification of histone peptides based on liquid chromatography–tandem mass spectrometry (LC–MS/MS) analysis. EpiProfile 2.0 is now optimized for data-independent acquisition through the use of precursor and fragment extracted ion chromatography to accurately determine the chromatographic profile and to discriminate isobaric forms of peptides. The software uses an intelligent retention time prediction trained on the analyzed samples to enable accurate peak detection. EpiProfile 2.0 supports label-free and isotopic labeling, different organisms, known sequence mutations in diseases, different derivatization strategies, and unusual PTMs (such as acyl-derived modifications). In summary, EpiProfile 2.0 is a universal and accurate platform for the quantification of histone marks via LC–MS/MS. Being the first software of its kind, we anticipate that EpiProfile 2.0 will play a fundamental role in epigenetic studies relevant to biology and translational medicine. EpiProfile is freely available at https://github.com/zfyuan/EpiProfile2.0_Family.
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