| Literature DB >> 32415747 |
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.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