Cell Permeable Ratiometric Fluorescent Sensors for Imaging Phosphoinositides

被引:16
作者
Mondal, Samsuzzoha [1 ]
Rakshit, Ananya [1 ]
Pal, Suranjana [2 ]
Dattat, Ankona [1 ]
机构
[1] Tata Inst Fundamental Res, Dept Chem Sci, Bombay 400005, Maharashtra, India
[2] Tata Inst Fundamental Res, Dept Biol Sci, Bombay 400005, Maharashtra, India
关键词
PHOSPHATIDYLINOSITOL 4,5-BISPHOSPHATE; PLASMA-MEMBRANE; BINDING PEPTIDES; LIVING CELLS; LIPID POOLS; GELSOLIN; DYNAMICS; PROTEINS; MULTIPLE; ORGANIZATION;
D O I
10.1021/acschembio.6b00067
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 are critical cell-signal mediators present on the plasma membrane. The dynamic change of phosphoinositide concentrations on the membrane including clustering and declustering mediates signal transduction. The importance of phosphoinositides is scored by the fact that they participate in almost all cell-signaling events, and a defect in phosphoinositide metabolism is linked to multiple diseases including cancer, bipolar disorder, and type 2 diabetes. Optical sensors for visualizing phosphoinositide distribution can provide information on phosphoinositide dynamics. This exercise will ultimately afford a handle into understanding and manipulating cell-signaling processes. The major requirement in phosphoinositide sensor development is a selective, cell permeable probe that can quantify phosphoinositides. To address this requirement, we have developed short peptide-based ratiometric fluorescent sensors for imaging phosphoinositides. The sensors afford a selective response toward two crucial signaling phosphoinositides, phosphatidylinositol-4,5-bisphosphate (PI(4,5)P2) and phosphatidylinositol-4-phosphate (PI4P), over other anionic membrane phospholipids and soluble inositol phosphates. Dissociation constant values indicate up to 4 times higher probe affinity toward PI(4,5)P2 when compared to PI4P. Significantly, the sensors are readily cell-permeable and enter cells within 15 min of incubation as indicated by multiphoton excitation confocal microscopy. Furthermore, the sensors light up signaling phosphoinositides present both on the cell membrane and on organelle membranes near the perinuclear space, opening avenues for quantifying and monitoring phosphoinositide signaling.
引用
收藏
页码:1834 / 1843
页数:10
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