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In Situ Quantitative Imaging of Cellular Lipids Using Molecular Sensors
Membrane lipids are dynamic molecules that play important roles in cell signaling and regulation but an in situ imaging method for quantitatively tracking lipids in living cells is lacking at present. Here we report a new chemical method of quantitative lipid imaging using sensors engineered by labe...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3205457/ https://www.ncbi.nlm.nih.gov/pubmed/22024883 http://dx.doi.org/10.1038/nchem.1163 |
Sumario: | Membrane lipids are dynamic molecules that play important roles in cell signaling and regulation but an in situ imaging method for quantitatively tracking lipids in living cells is lacking at present. Here we report a new chemical method of quantitative lipid imaging using sensors engineered by labeling proteins with an environmentally sensitive fluorophore. A prototype sensor for phosphatidylinositol-4,5-bisphosphate (PtdIns(4,5)P(2))– a key signaling lipid in diverse cellular processes–was generated by covalently attaching a single 2-dimethylamino-6-acyl-naphthalene group to the N-terminal α-helix of the engineered epsin1 ENTH domain– a protein that selectively binds PtdIns(4,5)P(2). The sensor allows robust and sensitive in situ quantitative imaging in mammalian cells, providing new insight into the spatiotemporal dynamics and fluctuation of this key signaling lipid. Application of the sensor to immune cells reveals the presence of a local threshold PtdIns(4,5)P(2) concentration required for triggering phagocytosis. This sensor strategy is generally applicable to in situ quantification of other cellular lipids. |
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