作者
Martin Pelosse, Cécile Cottet-Rousselle, Cécile M Bidan, Aurélie Dupont, Kapil Gupta, Imre Berger, Uwe Schlattner
发表日期
2019/3/4
期刊
Nature communications
卷号
10
期号
1
页码范围
1038
出版商
Nature Publishing Group UK
简介
AMP-activated protein kinase AMPK senses and regulates cellular energy state. AMPK activation by increasing AMP and ADP concentrations involves a conformational switch within the heterotrimeric complex. This is exploited here for the construction of a synthetic sensor of cellular energetics and allosteric AMPK activation, AMPfret. Based on engineered AMPK fused to fluorescent proteins, the sensor allows direct, real-time readout of the AMPK conformational state by fluorescence resonance energy transfer (FRET). AMPfret faithfully and dynamically reports the binding of AMP and ADP to AMPK γ-CBS sites, competed by Mg2+-free ATP. FRET signals correlate with activation of AMPK by allosteric mechanisms and protection from dephosphorylation, attributed here to specific CBS sites, but does not require activation loop phosphorylation. Moreover, AMPfret detects binding of pharmacological compounds to the …
引用总数
201920202021202220232024373353
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