Kubatzky Katharina F, Gao Yue, Yu Dayoung
Department of Infectious Diseases, Medical Faculty Heidelberg, Medical Microbiology and Hygiene, Heidelberg University, 69120 Heidelberg, Germany.
Department of Infectious Diseases, University Hospital Heidelberg, 69120 Heidelberg, Germany.
Explor Target Antitumor Ther. 2023;4(6):1260-1285. doi: 10.37349/etat.2023.00196. Epub 2023 Dec 27.
Cells need to adapt their activities to extra- and intracellular signalling cues. To translate a received extracellular signal, cells have specific receptors that transmit the signal to downstream proteins so that it can reach the nucleus to initiate or repress gene transcription. Post-translational modifications (PTMs) of proteins are reversible or irreversible chemical modifications that help to further modulate protein activity. The most commonly observed PTMs are the phosphorylation of serine, threonine, and tyrosine residues, followed by acetylation, glycosylation, and amidation. In addition to PTMs that involve the modification of a certain amino acid (phosphorylation, hydrophobic groups for membrane localisation, or chemical groups like acylation), or the conjugation of peptides (SUMOylation, NEDDylation), structural changes such as the formation of disulphide bridge, protein cleavage or splicing can also be classified as PTMs. Recently, it was discovered that metabolites from the tricarboxylic acid (TCA) cycle are not only intermediates that support cellular metabolism but can also modify lysine residues. This has been shown for acetate, succinate, and lactate, among others. Due to the importance of mitochondria for the overall fitness of organisms, the regulatory function of such PTMs is critical for protection from aging, neurodegeneration, or cardiovascular disease. Cancer cells and activated immune cells display a phenotype of accelerated metabolic activity known as the Warburg effect. This metabolic state is characterised by enhanced glycolysis, the use of the pentose phosphate pathway as well as a disruption of the TCA cycle, ultimately causing the accumulation of metabolites like citrate, succinate, and malate. Succinate can then serve as a signalling molecule by directly interacting with proteins, by binding to its G protein-coupled receptor 91 (GPR91) and by post-translationally modifying proteins through succinylation of lysine residues, respectively. This review is focus on the process of protein succinylation and its importance in health and disease.
细胞需要使其活动适应细胞外和细胞内的信号线索。为了转导接收到的细胞外信号,细胞具有特定的受体,这些受体将信号传递给下游蛋白质,以便信号能够到达细胞核以启动或抑制基因转录。蛋白质的翻译后修饰(PTM)是可逆或不可逆的化学修饰,有助于进一步调节蛋白质活性。最常见的PTM是丝氨酸、苏氨酸和酪氨酸残基的磷酸化,其次是乙酰化、糖基化和酰胺化。除了涉及特定氨基酸修饰(磷酸化、用于膜定位的疏水基团或酰化等化学基团)或肽缀合(SUMO化、NEDD化)的PTM外,诸如二硫键形成、蛋白质切割或剪接等结构变化也可归类为PTM。最近发现,三羧酸(TCA)循环的代谢产物不仅是支持细胞代谢的中间体,还可以修饰赖氨酸残基。乙酸盐、琥珀酸盐和乳酸盐等均已证明有此作用。由于线粒体对生物体整体健康的重要性,此类PTM的调节功能对于预防衰老、神经退行性疾病或心血管疾病至关重要。癌细胞和活化的免疫细胞表现出一种代谢活动加速的表型,即瓦伯格效应。这种代谢状态的特征是糖酵解增强、磷酸戊糖途径的利用以及TCA循环的破坏,最终导致柠檬酸盐、琥珀酸盐和苹果酸盐等代谢产物的积累。然后,琥珀酸盐可以分别通过与蛋白质直接相互作用、与G蛋白偶联受体91(GPR91)结合以及通过赖氨酸残基的琥珀酰化对蛋白质进行翻译后修饰,从而作为信号分子发挥作用。本综述重点关注蛋白质琥珀酰化过程及其在健康和疾病中的重要性。