Literature DB >> 32415747

A photostable monomeric superfolder green fluorescent protein.

Fernando M Valbuena1, Ivy Fitzgerald2, Rita L Strack1, Neal Andruska1, Luke Smith1, Benjamin S Glick1.   

Abstract

The green fluorescent protein (GFP) from Aequorea victoria has been engineered extensively in the past to generate variants suitable for protein tagging. Early efforts produced the enhanced variant EGFP and its monomeric derivative mEGFP, which have useful photophysical properties, as well as superfolder GFP, which folds efficiently under adverse conditions. We previously generated msGFP, a monomeric superfolder derivative of EGFP. Unfortunately, compared to EGFP, msGFP and other superfolder GFP variants show faster photobleaching. We now describe msGFP2, which retains monomeric superfolder properties while being as photostable as EGFP. msGFP2 contains modified N- and C-terminal peptides that are expected to reduce nonspecific interactions. Compared to EGFP and mEGFP, msGFP2 is less prone to disturbing the functions of certain partner proteins. For general-purpose protein tagging, msGFP2 may be the best available derivative of A. victoria GFP.
© 2020 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

Entities:  

Keywords:  GFP; cytotoxicity; fluorescent protein; mCherry; mScarlet; monomeric; photobleaching; superfolder

Mesh:

Substances:

Year:  2020        PMID: 32415747      PMCID: PMC7508230          DOI: 10.1111/tra.12737

Source DB:  PubMed          Journal:  Traffic        ISSN: 1398-9219            Impact factor:   6.215


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