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Literature DB >> 16278647

Photoconversion of YFP into a CFP-like species during acceptor photobleaching FRET experiments.

Guillaume Valentin, Céline Verheggen, Tristan Piolot, Henry Neel, Maïté Coppey-Moisan, Edouard Bertrand.

Abstract

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Year: 2005 PMID： 16278647 DOI： 10.1038/nmeth1105-801

Source DB: PubMed Journal: Nat Methods ISSN： 1548-7091 Impact factor: 28.547

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36 in total

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3. Probing novel GPCR interactions using a combination of FRET and TIRF.

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4. Kinesin-1 structural organization and conformational changes revealed by FRET stoichiometry in live cells.

Authors: Dawen Cai; Adam D Hoppe; Joel A Swanson; Kristen J Verhey
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5. Spatial distribution of protein kinase A activity during cell migration is mediated by A-kinase anchoring protein AKAP Lbc.

Authors: Adriana A Paulucci-Holthauzen; Leoncio A Vergara; Larry J Bellot; David Canton; John D Scott; Kathleen L O'Connor
Journal: J Biol Chem Date: 2008-12-23 Impact factor: 5.157

Photoconversion of YFP into a CFP-like species during acceptor photobleaching FRET experiments.

1. Application of fluorescence resonance energy transfer in protein studies.

2. Correlating calcium binding, Förster resonance energy transfer, and conformational change in the biosensor TN-XXL.

3. Probing novel GPCR interactions using a combination of FRET and TIRF.

4. Kinesin-1 structural organization and conformational changes revealed by FRET stoichiometry in live cells.

5. Spatial distribution of protein kinase A activity during cell migration is mediated by A-kinase anchoring protein AKAP Lbc.

6. Time-resolved FRET fluorescence spectroscopy of visible fluorescent protein pairs.

7. Bridging the spectral gap in fluorescent proteins through directed evolution.

Review 8. New strategies for fluorescent probe design in medical diagnostic imaging.

9. Human ACE and bradykinin B2 receptors form a complex at the plasma membrane.

Review 10. The fluorescent protein palette: tools for cellular imaging.