Fluorescent Biosensors for Multiplexed Imaging of Phosphoinositide Dynamics

被引:25
作者
Hertel, Fabian [1 ,5 ]
Li, Simin [1 ]
Chen, Mingyuan [2 ]
Pott, Lutz [4 ]
Mehta, Sohum [1 ]
Zhang, Jin [1 ,2 ,3 ]
机构
[1] Univ Calif San Diego, Dept Pharmacol, La Jolla, CA 92093 USA
[2] Univ Calif San Diego, Dept Bioengn, La Jolla, CA 92093 USA
[3] Univ Calif San Diego, Dept Chem & Biochem, La Jolla, CA 92093 USA
[4] Ruhr Univ Bochum, Inst Physiol, D-44801 Bochum, Germany
[5] Univ Hosp RWTH Aachen, Dept Nucl Med, Aachen, Germany
关键词
PHOSPHOLIPASE-C; RECEPTOR; INHIBITOR; 3-KINASE; BINDING; DOMAINS;
D O I
10.1021/acschembio.9b00691
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
Phosphoinositides constitute a critical family of lipids that regulate numerous cellular processes. Phosphatidylinositol 4,5-bisphosphate (PIP2) is arguably the most important plasma membrane phosphoinositide and is involved in regulating diverse processes. It is also the precursor of phosphatidylinositol 3,4,5-trisphosphate (PIP3), which is critical for growth factor signaling, as well as membrane polarization and dynamics. Studying these lipids remains challenging, because of their compartmentalized activities and location-dependent signaling profiles. Here, we introduce several new genetically encoded fluorescent biosensors, including FRET-based and dimerization-dependent fluorescent protein (ddFP)-based biosensors, that enable real-time monitoring of PIP2 levels in live cells. In addition, we developed a red fluorescent biosensor for 3-phosphoinositides that can be co-imaged with the green PIP2 indicator. Simultaneous visualization of the dynamics of PIP2 and 3-phosphoinositides in the same cell shows that plasma membrane PIP3 formation upon EGF stimulation is coupled to a decrease in the local pool of PIP2.
引用
收藏
页码:33 / 38
页数:6
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