Guangxi Key Laboratory of Metabolic Disease Research, Department of Clinical Laboratory of Guilin No. 924 Hospital, Guilin 541002, Guangxi, China.
Clinical Medical Research Center, The Second Clinical Medical College of Jinan University, Shenzhen People's Hospital, Shenzhen, Guangdong 518020, China.
Can Respir J. 2021 Jun 15;2021:6652297. doi: 10.1155/2021/6652297. eCollection 2021.
The modification of lysine crotonylation (Kcr) is another biological function of histone in addition to modification of lysine acetylation (Kac), which may play a specific regulatory role in diseases.
This study compared the expression levels of Kcr and proteome between patients with chronic obstructive pulmonary disease (COPD) combined with type II respiratory failure (RF) to study the relationship between Kcr, proteome, and COPD.
We tested the Kcr and proteome of COPD combined with type II RF and normal control (NC) using croton acylation enrichment technology and liquid chromatography tandem mass spectrometry (LC-MS/MS) with high resolution.
We found that 32 sites of 23 proteins were upregulated and 914 sites of 295 proteins were downregulated. We performed Kyoto Encyclopedia of Genes and Genomes (KEGG), protein domain, and Gene Ontology (GO) analysis on crotonylated protein. In proteomics research, we found that 190 proteins were upregulated and 151 proteins were downregulated. Among them, 90 proteins were both modified by differentially expressed crotonylation sites and differentially expressed in COPD combined with type II RF and NC.
Differentially expressed crotonylation sites may be involved in the development of COPD combined with type II RF. 90 proteins modified by crotonylation and differentially expressed in COPD combined with type II RF can be used as markers for the study of the molecular pathogenesis of COPD combined with type II RF.
赖氨酸丙二酰化(Kcr)的修饰是除赖氨酸乙酰化(Kac)修饰之外,组蛋白的另一种生物学功能,它可能在疾病中发挥特定的调节作用。
本研究比较了慢性阻塞性肺疾病(COPD)合并 II 型呼吸衰竭(RF)患者的 Kcr 和蛋白质组表达水平,以研究 Kcr、蛋白质组与 COPD 之间的关系。
我们使用丙二酰化富集技术和液相色谱串联质谱(LC-MS/MS)结合高分辨率检测 COPD 合并 II 型 RF 患者和正常对照(NC)的 Kcr 和蛋白质组。
我们发现 23 个蛋白的 32 个位点上调,295 个蛋白的 914 个位点下调。我们对丙二酰化蛋白进行了京都基因与基因组百科全书(KEGG)、蛋白质结构域和基因本体论(GO)分析。在蛋白质组学研究中,我们发现 190 个蛋白上调,151 个蛋白下调。其中,90 个蛋白同时被差异表达的丙二酰化位点和 COPD 合并 II 型 RF 和 NC 中的差异表达所修饰。
差异表达的丙二酰化位点可能参与了 COPD 合并 II 型 RF 的发生发展。在 COPD 合并 II 型 RF 中,丙二酰化和差异表达的 90 个蛋白可以作为研究 COPD 合并 II 型 RF 分子发病机制的标志物。