| Literature DB >> 33988507 |
Haitao Zhang1,2, Xiaolei Cao1, Mei Tang1, Guoxuan Zhong1, Yuan Si1, Haidong Li3, Feifeng Zhu1, Qinghua Liao1, Liuju Li4, Jianhui Zhao5, Jia Feng6, Shuaifeng Li1, Chenliang Wang1, Manuel Kaulich7, Fangwei Wang1,2, Liangyi Chen4, Li Li8, Zongping Xia1, Tingbo Liang2,5, Huasong Lu1,2, Xin-Hua Feng1,2, Bin Zhao1,2,5.
Abstract
The human kinome comprises 538 kinases playing essential functions by catalyzing protein phosphorylation. Annotation of subcellular distribution of the kinome greatly facilitates investigation of normal and disease mechanisms. Here, we present Kinome Atlas (KA), an image-based map of the kinome annotated to 10 cellular compartments. 456 epitope-tagged kinases, representing 85% of the human kinome, were expressed in HeLa cells and imaged by immunofluorescent microscopy under a similar condition. KA revealed kinase family-enriched subcellular localizations and discovered a collection of new kinase localizations at mitochondria, plasma membrane, extracellular space, and other structures. Furthermore, KA demonstrated the role of liquid-liquid phase separation in formation of kinase condensates. Identification of MOK as a mitochondrial kinase revealed its function in cristae dynamics, respiration, and oxidative stress response. Although limited by possible mislocalization due to overexpression or epitope tagging, this subcellular map of the kinome can be used to refine regulatory mechanisms involving protein phosphorylation.Entities:
Keywords: MOK; biochemistry; cell biology; chemical biology; human; kinome; mitochondrial; phase separation; subcellular localization
Year: 2021 PMID: 33988507 PMCID: PMC8175086 DOI: 10.7554/eLife.64943
Source DB: PubMed Journal: Elife ISSN: 2050-084X Impact factor: 8.140