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Please use this identifier to cite or link to this item: http://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/3301
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dc.contributor.authorAddy, Partha Sarathi-
dc.date.accessioned2021-11-11T10:54:45Z-
dc.date.available2021-11-11T10:54:45Z-
dc.date.issued2017-01-17-
dc.identifier.urihttps://chemistry-europe.onlinelibrary.wiley.com/doi/10.1002/cbic.201600668-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/3301-
dc.description.abstractFörster resonance energy transfer (FRET) between two suitable fluorophores is a powerful tool to monitor dynamic changes in protein structure in vitro and in vivo. The ability to genetically encode a FRET pair represents a convenient “labeling-free” strategy to incorporate them into target protein(s). Currently, the only genetically encoded FRET pairs available for use in mammalian cells use fluorescent proteins. However, their large size can lead to unfavorable perturbations, particularly when two are used at the same time. Additionally, fluorescent proteins are largely restricted to a terminal attachment to the target, which might not be optimal. Here, we report the development of an alternative genetically encoded FRET pair in mammalian cells that circumvents these challenges by taking advantage of a small genetically encoded fluorescent unnatural amino acid as the donor and enhanced green fluorescent protein (EGFP) as the acceptor. The small size of Anap relative to fluorescent proteins, and the ability to co-translationally incorporate it into internal sites on the target protein, endows this novel FRET pair with improved versatility over its counterparts that rely upon two fluorescent proteins.en_US
dc.language.isoenen_US
dc.publisherWileyen_US
dc.subjectChemistryen_US
dc.subjectMammalian Cellsen_US
dc.subjectFörster resonance energy transfer (FRET)en_US
dc.titleA Unique Genetically Encoded FRET Pair in Mammalian Cellsen_US
dc.typeArticleen_US
Appears in Collections:Department of Chemistry

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