Tsutsumi Ryouhei, Fukata Yuko, Fukata Masaki
Division of Membrane Physiology, Department of Cell Physiology, National Institute for Physiological Sciences, 5-1 Higashiyama, Myodaiji, Okazaki, Aichi, 444-8787, Japan.
Pflugers Arch. 2008 Sep;456(6):1199-206. doi: 10.1007/s00424-008-0465-x. Epub 2008 Jan 30.
Posttranslational modification provides proteins with additional function and regulatory control beyond genomic information, allowing cells to maintain homeostasis and respond to extracellular signals. Protein palmitoylation, the common posttranslational modification with the lipid palmitate, plays a pivotal role in protein trafficking and function. Palmitoylation is unique in that it is reversible and dynamically regulated by specific extracellular signals. The reversible nature of protein palmitoylation enables proteins to shuttle between intracellular compartments upon extracellular signals. However, the molecular mechanisms of protein palmitoylation have long been elusive, mostly because the enzymes responsible for protein palmitoylation were unknown. Recently, genetically conserved DHHC family proteins have emerged as palmitoyl-acyl transferases. With the identification of specific enzymes for palmitoylated proteins, including H-Ras, PSD-95, and eNOS, the specificity and regulatory mechanism of DHHC enzymes are beginning to be clarified.
翻译后修饰为蛋白质提供了超越基因组信息的额外功能和调控控制,使细胞能够维持体内平衡并响应细胞外信号。蛋白质棕榈酰化是一种常见的蛋白质与棕榈酸的翻译后修饰,在蛋白质运输和功能中起着关键作用。棕榈酰化的独特之处在于它是可逆的,并受到特定细胞外信号的动态调节。蛋白质棕榈酰化的可逆性使蛋白质能够在细胞外信号作用下在细胞内区室之间穿梭。然而,蛋白质棕榈酰化的分子机制长期以来一直难以捉摸,主要是因为负责蛋白质棕榈酰化的酶尚不清楚。最近,基因保守的DHHC家族蛋白已被确认为棕榈酰酰基转移酶。随着包括H-Ras、PSD-95和eNOS在内的棕榈酰化蛋白特异性酶的鉴定,DHHC酶的特异性和调控机制开始得到阐明。