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多聚谷氨酰化:生物学与分析。

Polyglutamylation: biology and analysis.

机构信息

Moderna Therapeutics, 200 Technology Square, Cambridge, MA, 02139, USA.

New England Biolabs, 240 County Rd, Ipswich, MA, 01938, USA.

出版信息

Amino Acids. 2022 Apr;54(4):529-542. doi: 10.1007/s00726-022-03146-4. Epub 2022 Mar 31.

Abstract

Polyglutamylation is a posttranslational modification (PTM) that adds several glutamates on glutamate residues in the form of conjugated peptide chains by a family of enzymes known as polyglutamylases. Polyglutamylation is well documented in microtubules. Polyglutamylated microtubules consist of different α- and β-tubulin subunits with varied number of added glutamate residues. Kinetic control and catalytic rates of tubulin modification by polyglutamylases influence the polyglutamylation pattern of functional microtubules. The recent studies uncovered catalytic mechanisms of the glutamylation enzymes family, particularly tubulin tyrosine ligase-like (TTLL). Variable length polyglutamylation of primary sequence glutamyl residues have been mapped with a multitude of protein chemistry and proteomics approaches. Although polyglutamylation was initially considered a tubulin-specific modification, the recent studies have uncovered a calmodulin-dependent glutamylase, SidJ. Nano-electrospray ionization (ESI) proteomic approaches have identified quantifiable polyglutamylated sites in specific substrates. Indeed, conjugated glutamylated peptides were used in nano-liquid chromatography gradient delivery due to their relative hydrophobicity for their tandem mass spectrometry (MS/MS) characterization. The recent polyglutamylation characterization has revealed three major sites: E445 in α-tubulin, E435 in β-tubulin, and E860 in SdeA. In this review, we have summarized the progress made using proteomic approaches for large-scale detection of polyglutamylated peptides, including biology and analysis.

摘要

多聚谷氨酸化是一种翻译后修饰(PTM),通过一组称为多聚谷氨酸酶的酶,在谷氨酸残基上以共轭肽链的形式添加几个谷氨酸。多聚谷氨酸化在微管中已有充分的记载。多聚谷氨酸化的微管由不同数量的添加谷氨酸残基的α-和β-微管蛋白亚基组成。多聚谷氨酸酶对微管蛋白的修饰的动力学控制和催化速率影响功能性微管的多聚谷氨酸化模式。最近的研究揭示了谷氨酸酶家族的催化机制,特别是微管酪氨酸连接酶样(TTLL)。通过多种蛋白质化学和蛋白质组学方法,已经映射了初级序列谷氨酸残基的可变长度多聚谷氨酸化。虽然多聚谷氨酸化最初被认为是一种微管特异性修饰,但最近的研究揭示了一种钙调蛋白依赖性谷氨酸酶,即 SidJ。纳升电喷雾电离(ESI)蛋白质组学方法已经在特定底物中鉴定出可量化的多聚谷氨酸化位点。事实上,由于共轭谷氨酸化肽的相对疏水性,它们被用于纳升液相色谱梯度洗脱,以便进行串联质谱(MS/MS)分析。最近的多聚谷氨酸化特征分析揭示了三个主要位点:α-微管蛋白中的 E445、β-微管蛋白中的 E435 和 SdeA 中的 E860。在这篇综述中,我们总结了使用蛋白质组学方法进行大规模检测多聚谷氨酸化肽的生物学和分析方面的进展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a12d/9117372/9db0de70aadf/726_2022_3146_Fig1_HTML.jpg

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