Introduction Cells can sense and respond to the mechanical microenvironment by converting forces into biochemical signals inside the cells,i.e.mechanotransduction<sup>[1-3]</sup>.Focal adhesions are the ma...Introduction Cells can sense and respond to the mechanical microenvironment by converting forces into biochemical signals inside the cells,i.e.mechanotransduction<sup>[1-3]</sup>.Focal adhesions are the major sites of interaction between a cell and its extracellular matrix（ECM）microenvironment,thus outside mechanical signals can be sensed at focal adhesions through transmembrane receptor integrins.In particular,it has been shown that matrix elasticity can control the cell fate<sup>[4]</sup>by modulating the interactions between ECM proteins and their receptor integrins<sup>[5,6]</sup>.For example,different rigidity of polyacrylamide（PA）gels can lead to different density of ECM ancho-展开更多
Genetically encoded biosensors based on fluorescence resonance energy transfer(FRET)have been widely applied to visualize the molecular activity in live cells with high spatiotemporal resolution.The enormous amount of...Genetically encoded biosensors based on fluorescence resonance energy transfer(FRET)have been widely applied to visualize the molecular activity in live cells with high spatiotemporal resolution.The enormous amount of video images and the complex dynamics of signaling events present tremendous challenges for data analysis and demand the development of intelligent and automated imaging analysis methods specifically envisioned for the studies of live cell imaging.We have developed a general correlative FRET imaging method(CFIM)to quantify the subcellular coupling between an enzymatic activity and a phenotypic response in live cells,e.g.at focal adhesions(FAs).CFIM quantitatively evaluated the cause-effect relation-展开更多
基金supported in part by NIH HL098472NSF CBET0846429
文摘Introduction Cells can sense and respond to the mechanical microenvironment by converting forces into biochemical signals inside the cells,i.e.mechanotransduction<sup>[1-3]</sup>.Focal adhesions are the major sites of interaction between a cell and its extracellular matrix（ECM）microenvironment,thus outside mechanical signals can be sensed at focal adhesions through transmembrane receptor integrins.In particular,it has been shown that matrix elasticity can control the cell fate<sup>[4]</sup>by modulating the interactions between ECM proteins and their receptor integrins<sup>[5,6]</sup>.For example,different rigidity of polyacrylamide（PA）gels can lead to different density of ECM ancho-
文摘Genetically encoded biosensors based on fluorescence resonance energy transfer(FRET)have been widely applied to visualize the molecular activity in live cells with high spatiotemporal resolution.The enormous amount of video images and the complex dynamics of signaling events present tremendous challenges for data analysis and demand the development of intelligent and automated imaging analysis methods specifically envisioned for the studies of live cell imaging.We have developed a general correlative FRET imaging method(CFIM)to quantify the subcellular coupling between an enzymatic activity and a phenotypic response in live cells,e.g.at focal adhesions(FAs).CFIM quantitatively evaluated the cause-effect relation-
