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Study and selection of in vivo protein interactions by coupling bimolecular fluorescence complementation and flow cytometry.

Study and selection of in vivo protein interactions by coupling bimolecular fluorescence complementation and flow cytometry. Research Abstract Details 

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  • Study and selection of in vivo protein interactions by coupling bimolecular fluorescence complementation and flow cytometry. Abstract Text:

    montse morellMontse Morell,alba espargaroAlba Espargaro,francesc xavier avilesFrancesc Xavier Aviles,salvador venturaSalvador Ventura,montse morellMontse Morell,alba espargaroAlba Espargaro,francesc xavier avilesFrancesc Xavier Aviles,salvador venturaSalvador Ventura,montse morellMontse Morell,alba espargaroAlba Espargaro,francesc xavier avilesFrancesc Xavier Aviles,salvador venturaSalvador Ventura,montse morellMontse Morell,alba espargaroAlba Espargaro,francesc xavier avilesFrancesc Xavier Aviles,salvador venturaSalvador Ventura,

    We present a high-throughput approach to study weak protein-protein interactions by coupling bimolecular fluorescent complementation (BiFC) to flow cytometry (FC). In BiFC, the interaction partners (bait and prey) are fused to two rationally designed fragments of a fluorescent protein, which recovers its function upon the binding of the interacting proteins. For weak protein-protein interactions, the detected fluorescence is proportional to the interaction strength, thereby allowing in vivo discrimination between closely related binders with different affinity for the bait protein. FC provides a method for high-speed multiparametric data acquisition and analysis; the assay is simple, thousands of cells can be analyzed in seconds and, if required, selected using fluorescence-activated cell sorting (FACS). The combination of both methods (BiFC-FC) provides a technically straightforward, fast and highly sensitive method to validate weak protein interactions and to screen and identify optimal ligands in biologically synthesized libraries. Once plasmids encoding the protein fusions have been obtained, the evaluation of a specific interaction, the generation of a library and selection of active partners using BiFC-FC can be accomplished in 5 weeks.

    Study and selection of in vivo protein interactions by coupling bimolecular fluorescence complementation and flow cytometry. Publishing Authors By Initials

    m morellM Morell,a espargaroA Espargaro,fx avilesFX Aviles,s venturaS Ventura,m morellM Morell,a espargaroA Espargaro,fx avilesFX Aviles,s venturaS Ventura,m morellM Morell,a espargaroA Espargaro,fx avilesFX Aviles,s venturaS Ventura,m morellM Morell,a espargaroA Espargaro,fx avilesFX Aviles,s venturaS Ventura,

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    Study and selection of in vivo protein interactions by coupling bimolecular fluorescence complementation and flow cytometry. Journal Published:

    PUBLICATION TYPE: Journal Article

    Journal: Nature protocols

    VOLUME: 3

    Page Numbers: 22-33

    Journal Abbreviation:

    ISSN: 1750-2799

    DAY: 14

    MONTH: 01

    YEAR: 2008

    Study and selection of in vivo protein interactions by coupling bimolecular fluorescence complementation and flow cytometry. Information

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    LANGUAGE: eng

    NlmUniqueID: 101284307

    Study and selection of in vivo protein interactions by coupling bimolecular fluorescence complementation and flow cytometry. Keywords Mesh Terms:

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    Grant and Affiliation Information for Study and selection of in vivo protein interactions by coupling bimolecular fluorescence complementation and flow cytometry.

    AFFILIATION: Institut de Biotecnologia i de Biomedicina, Universitat Autònoma de Barcelona, E-08193 Bellaterra, Spain.

    Country: England

    England Research PublicationEngland Research Publication

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    MEDLINETA: Nat Protoc

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