Parks Anastacia R, Escalante-Semerena Jorge C
Department of Microbiology, University of Georgia, Athens, GA 30606, USA.
Curr Trends Microbiol. 2022;16:1-18. doi: 10.31300/ctmb.16.2022.1-18.
N-terminal (Nt)-acylation is the irreversible addition of an acyl moiety to the terminal alpha amino group of a peptide chain. This type of modification alters the nature of the N terminus, which can interfere with the function of the modified protein by disrupting protein interactions, function, localization, degradation, hydrophobicity, or charge. Nt acylation is found in all domains of life and is a highly common occurrence in eukaryotic cells. However, in prokaryotes very few cases of Nt acylation have been reported. It was once thought that Nt acylation of proteins, other than ribosomal proteins, was uncommon in prokaryotes, but recent evidence suggests that this modification may be more common than once realized. In this review, we discuss what is known about prokaryotic Nt acetylation and the acetyltransferases that are responsible, as well as recent advancements in this field and currently used methods to study Nt acetylation.
N 端(Nt)酰化是指将一个酰基部分不可逆地添加到肽链的末端α氨基上。这种修饰类型改变了 N 端的性质,可能会通过破坏蛋白质相互作用、功能、定位、降解、疏水性或电荷来干扰修饰后蛋白质的功能。Nt 酰化存在于所有生命领域,在真核细胞中非常普遍。然而,在原核生物中,报道的 Nt 酰化情况很少。曾经有人认为,除核糖体蛋白外,蛋白质的 Nt 酰化在原核生物中并不常见,但最近的证据表明,这种修饰可能比以前认为的更为普遍。在这篇综述中,我们讨论了关于原核生物 Nt 乙酰化及其相关乙酰转移酶的已知信息,以及该领域的最新进展和目前用于研究 Nt 乙酰化的方法。