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  Trifunctional lipid probes for comprehensive studies of single lipid species in living cells.

Höglinger, D., Nadler, A., Haberkant, P., Kirkpatrick, J., Schifferer, M., Stein, F., et al. (2017). Trifunctional lipid probes for comprehensive studies of single lipid species in living cells. Proceedings of the National Academy of Sciences of the United States of America, 114(7), 1566-1571. doi:10.1073/pnas.1611096114.

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Höglinger, Doris, Author
Nadler, André1, Author           
Haberkant, Per, Author
Kirkpatrick, Joanna, Author
Schifferer, Martina, Author
Stein, Frank, Author
Hauke, Sebastian, Author
Porter, Forbes D, Author
Schultz, Carsten, Author
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1Max Planck Institute for Molecular Cell Biology and Genetics, ou_2340692              

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 Abstract: Lipid-mediated signaling events regulate many cellular processes. Investigations of the complex underlying mechanisms are difficult because several different methods need to be used under varying conditions. Here we introduce multifunctional lipid derivatives to study lipid metabolism, lipid-protein interactions, and intracellular lipid localization with a single tool per target lipid. The probes are equipped with two photoreactive groups to allow photoliberation (uncaging) and photo-cross-linking in a sequential manner, as well as a click-handle for subsequent functionalization. We demonstrate the versatility of the design for the signaling lipids sphingosine and diacylglycerol; uncaging of the probe for these two species triggered calcium signaling and intracellular protein translocation events, respectively. We performed proteomic screens to map the lipid-interacting proteome for both lipids. Finally, we visualized a sphingosine transport deficiency in patient-derived Niemann-Pick disease type C fibroblasts by fluorescence as well as correlative light and electron microscopy, pointing toward the diagnostic potential of such tools. We envision that this type of probe will become important for analyzing and ultimately understanding lipid signaling events in a comprehensive manner.

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 Dates: 2017-02-14
 Publication Status: Issued
 Pages: -
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 Rev. Type: -
 Identifiers: DOI: 10.1073/pnas.1611096114
Other: cbg-6763
PMID: 28154130
 Degree: -

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Title: Proceedings of the National Academy of Sciences of the United States of America
  Other : Proc Natl Acad Sci U.S.A.
Source Genre: Journal
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Pages: - Volume / Issue: 114 (7) Sequence Number: - Start / End Page: 1566 - 1571 Identifier: -