Fuller Cassandra N, Mansoor Sabrina, Guzman Santiago J, Tose Lilian Valadares, Hackerott Serena, Rodriguez-Casariego Javier, Eirin-Lopez Jose M, Fernandez-Lima Francisco
Department of Chemistry and Biochemistry, Florida International University, Miami, FL 33199, United States.
Environmental Epigenetics Laboratory, Institute of Environment, Florida International University, Miami, FL 33199, United States.
Environ Epigenet. 2025 May 29;11(1):dvaf017. doi: 10.1093/eep/dvaf017. eCollection 2025.
Histone post-translational modifications (PTMs) participate in the dynamic regulation of chromatin structure and function, through their chemical nature and specific location within the histone sequence. Alternative analytical approaches for histone PTM studies are required to facilitate the differentiation between ubiquitously present isomers and the detection of low-abundance PTMs Here, we report a high-sensitivity bottom-up method based on nano-liquid chromatography (nLC), trapped ion mobility spectrometry (TIMS), data-dependent acquisition (DDA), parallel accumulation-serial fragmentation (PASEF), and high-resolution time-of-flight tandem mass spectrometry (ToF-MS/MS) for the analysis of histone PTMs. This method was tested in a threatened coral species, the staghorn coral , during an episode of acute thermal stress. The obtained results allowed for the identification of PTM changes in core histones involved in the coral's heat response. Compared to traditional LC-MS/MS approaches, the incorporation of TIMS and ddaPASEF MS/MS resulted in a highly specific and sensitive method with a wide dynamic range (6 orders of magnitude). This depth of analysis allows for the simultaneous measurement of low-abundance PTM signatures relative to the unmodified form. An added advantage is the ability to mass- and mobility-isolate prior to peptide sequencing, resulting in higher confidence identification of epigenetic markers associated with heat stress in corals (e.g. increased H4 4-17 with 2ac and 3ac, and decreases in H4 4-17 K12ac, K16ac, H4 K20me, and H2A K5ac, K7ac, K9ac, K12ac, K14ac, and K74ac).
组蛋白翻译后修饰(PTMs)通过其化学性质和在组蛋白序列中的特定位置,参与染色质结构和功能的动态调节。需要采用替代分析方法来研究组蛋白PTMs,以促进普遍存在的异构体之间的区分以及低丰度PTMs的检测。在此,我们报告一种基于纳升液相色谱(nLC)、阱式离子淌度质谱(TIMS)、数据依赖采集(DDA)、平行累积-序列碎裂(PASEF)和高分辨率飞行时间串联质谱(ToF-MS/MS)的高灵敏度自下而上方法,用于分析组蛋白PTMs。该方法在鹿角珊瑚这种受威胁的珊瑚物种处于急性热应激事件期间进行了测试。获得的结果有助于鉴定参与珊瑚热反应的核心组蛋白中的PTM变化。与传统的液相色谱-串联质谱(LC-MS/MS)方法相比,结合TIMS和ddaPASEF MS/MS形成了一种具有高特异性和高灵敏度、宽动态范围(6个数量级)的方法。这种深度分析能够同时测量相对于未修饰形式的低丰度PTM特征。另一个优势是在肽测序之前能够进行质量和淌度分离,从而更有信心地鉴定与珊瑚热应激相关的表观遗传标记(例如,H4 4 - 17位点的2ac和3ac增加,以及H4 4 - 17位点的K12ac、K16ac、H4 K20me,和H2A K5ac、K7ac、K9ac、K12ac、K14ac以及K74ac减少)。