Towards a Functional Understanding of Protein N-Terminal Acetylation

被引:155
作者
Arnesen, Thomas [1 ,2 ]
机构
[1] Univ Bergen, Dept Mol Biol, Bergen, Norway
[2] Haukeland Hosp, Dept Surg, N-5021 Bergen, Norway
关键词
SIGNAL RECOGNITION PARTICLE; INTEGRAL MEMBRANE-PROTEIN; SACCHAROMYCES-CEREVISIAE; ENDOPLASMIC-RETICULUM; ACETYLTRANSFERASE NATB; ALPHA-ACETYLATION; TUMOR-SUPPRESSOR; GTPASE ARL3P; YEAST; DEGRADATION;
D O I
10.1371/journal.pbio.1001074
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Protein N-terminal acetylation is a major modification of eukaryotic proteins. Its functional implications include regulation of protein-protein interactions and targeting to membranes, as demonstrated by studies of a handful of proteins. Fifty years after its discovery, a potential general function of the N-terminal acetyl group carried by thousands of unique proteins remains enigmatic. However, recent functional data suggest roles for N-terminal acetylation as a degradation signal and as a determining factor for preventing protein targeting to the secretory pathway, thus highlighting N-terminal acetylation as a major determinant for the life and death of proteins. These contributions represent new and intriguing hypotheses that will guide the research in the years to come.
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页数:5
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