In situ quantitative imaging of cellular lipids using molecular sensors

Abstract

Membrane lipids are dynamic molecules that play important roles in cell signalling 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 labelling proteins with an environmentally sensitive fluorophore. A prototype sensor for phosphatidylinositol-4,5-bisphosphate (PtdIns(4,5)P2)—a key signalling 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)P2. 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 signalling lipid. Application of the sensor to immune cells reveals the presence of a local threshold PtdIns(4,5)P2 concentration required for triggering phagocytosis. This sensor strategy is generally applicable to in situ quantification of other cellular lipids. Cellular membrane lipids play key roles in cell regulation. Here, an environmentally sensitive fluorophore is attached to a protein that binds to a key signalling lipid to produce a membrane lipid sensor. This strategy allows sensitive, quantitative, spatiotemporal imaging of the lipid concentration in mammalian cells.

Cite this article

Yoon, Y., Lee, P., Kurilova, S. et al. In situ quantitative imaging of cellular lipids using molecular sensors. Nature Chem 3, 868–874 (2011). https://doi.org/10.1038/nchem.1163

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