Cell signaling regulation by protein phosphorylation: a multivariate, heterogeneous, and context-dependent process

被引:84
作者
Day, Evan K. [1 ]
Sosale, Nisha G. [1 ]
Lazzara, Matthew J. [1 ,2 ]
机构
[1] Univ Penn, Dept Chem & Biomol Engn, Philadelphia, PA 19104 USA
[2] Univ Penn, Dept Bioengn, Philadelphia, PA 19104 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
EPITHELIAL-MESENCHYMAL TRANSITION; TYROSINE PHOSPHATASES; ERK ACTIVITY; LUNG-CANCER; RECEPTOR; EGFR; NETWORKS; DYNAMICS; SRC; PROLIFERATION;
D O I
10.1016/j.copbio.2016.06.005
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Proper spatiotemporal regulation of protein phosphorylation in cells and tissues is required for normal development and homeostasis, but aberrant protein phosphorylation regulation leads to various diseases. The study of signaling regulation by protein phosphorylation is complicated in part by the sheer scope of the kinome and phosphoproteome, dependence of signaling protein functionality on cellular localization, and the complex multivariate relationships that exist between protein phosphorylation dynamics and the cellular phenotypes they control. Additional complexities arise from the ability of microenvironmental factors to influence phosphorylation-dependent signaling and from the tendency for some signaling processes to occur heterogeneously among cells. These considerations should be taken into account when measuring cell signaling regulation by protein phosphorylation.
引用
收藏
页码:185 / 192
页数:8
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