Cargando…
Optimising expression of the large dynamic range FRET pair mNeonGreen and superfolder mTurquoise2(ox) for use in the Escherichia coli cytoplasm
The fluorescent proteins superfolder mTurquoise2(ox) (sfTq2(ox)) and mNeonGreen function excellently in mammalian cells, but are not well expressed in E. coli when forming the N-terminus of constructs. Expression was increased by decreasing structures at the start of their coding sequences in the mR...
Autores principales: | Mertens, Laureen M. Y., den Blaauwen, Tanneke |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9606377/ https://www.ncbi.nlm.nih.gov/pubmed/36289441 http://dx.doi.org/10.1038/s41598-022-22918-2 |
Ejemplares similares
-
Superfolder mTurquoise2(ox) optimized for the bacterial periplasm allows high efficiency in vivo FRET of cell division antibiotic targets
por: Meiresonne, Nils Y., et al.
Publicado: (2019) -
Characterization of a spectrally diverse set of fluorescent proteins as FRET acceptors for mTurquoise2
por: Mastop, Marieke, et al.
Publicado: (2017) -
Endogenous expression and localization of HIS-72::mTurquoise2 in C. elegans
por: Sloan, Dillon E., et al.
Publicado: (2021) -
Comparing the performance of mScarlet-I, mRuby3, and mCherry as FRET acceptors for mNeonGreen
por: McCullock, Tyler W., et al.
Publicado: (2020) -
Cyan fluorescent proteins derived from mNeonGreen
por: Zarowny, Landon, et al.
Publicado: (2022)