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  A homogeneous fluorescence resonance energy transfer system for monitoring the activation of a protein switch in real time

Bill, A., Blockus, H., Stumpfe, D., Bajorath, J., Schmitz, A., & Famulok, M. (2011). A homogeneous fluorescence resonance energy transfer system for monitoring the activation of a protein switch in real time. Journal of the American Chemical Society, 133(21), 8372-9. doi:10.1021/ja202513s.

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Item Permalink: http://hdl.handle.net/11858/00-001M-0000-0028-6429-5 Version Permalink: http://hdl.handle.net/11858/00-001M-0000-0028-642A-3
Genre: Journal Article

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 Creators:
Bill, A., Author
Blockus, H., Author
Stumpfe, D., Author
Bajorath, J., Author
Schmitz, A., Author
Famulok, M.1, Author
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1External Organizations, ou_persistent22              

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Free keywords: ADP-Ribosylation Factor 1/*chemistry/pharmacology Adaptor Proteins, Vesicular Transport/*chemistry/pharmacology Cell Line, Tumor Cell Proliferation/drug effects Fluorescence Resonance Energy Transfer GTP Phosphohydrolases/*chemistry GTPase-Activating Proteins/chemistry Guanine Nucleotide Exchange Factors/chemistry Guanosine Diphosphate/metabolism Guanosine Triphosphate/metabolism Humans Protein Binding Tryptophan/chemistry
 Abstract: A homogeneous fluorescence resonance energy transfer (FRET) system for the real-time monitoring of exchange factor-catalyzed activation of a ras-like small GTPase is described. The underlying design is based on supramolecular template effects exerted by protein-protein interactions between the GTPase adenosine diphosphate ribosylation factor (ARF) and its effector protein GGA3. The GTPase is activated when bound to guanosine triphosphate (GTP) and switched off in its guanosine diphosphate (GDP)-bound state. Both states are accompanied by severe conformational changes that are recognized by GGA3, which only binds the GTPase "on" state. GDP-to-GTP exchange, i.e., GTPase activation, is catalyzed by the guanine nucleotide exchange factor cytohesin-2. When GGA3 and the GTPase ARF1 are labeled with thoroughly selected FRET probes, with simultaneous recording of the fluorescence of an internal tryptophan residue in ARF1, the conformational changes during the activation of the GTPase can be monitored in real time. We applied the FRET system to a multiplex format that allows the simultaneous identification and distinction of small-molecule inhibitors that interfere with the cytohesin-catalyzed ARF1 activation and/or with the interaction between activated ARF1-GTP and GGA3. By screening a library of potential cytohesin inhibitors, predicted by in silico modeling, we identified new inhibitors for the cytohesin-catalyzed GDP/GTP exchange on ARF1 and verified their increased potency in a cell proliferation assay.

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 Dates: 2011
 Publication Status: Published in print
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 Identifiers: Other: 21517092
DOI: 10.1021/ja202513s
ISSN: 1520-5126 (Electronic)
ISSN: 0002-7863 (Linking)
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Title: Journal of the American Chemical Society
  Alternative Title : J. Am. Chem. Soc.
Source Genre: Journal
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Pages: - Volume / Issue: 133 (21) Sequence Number: - Start / End Page: 8372 - 9 Identifier: -