Detecting stoichiometry of macromolecular complexes in live cells using FRET
Measuring thein vivo stoichiometry of protein-protein interactions is challenging. Here the authors take a FRET-based approach, quantifying stoichiometry based on ratiometric comparison of donor and acceptor fluorescence, and apply their method to report on a Ca2+-induced switch in calmodulin bindin...
Guardado en:
Autores principales: | Manu Ben-Johny, Daniel N. Yue, David T. Yue |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
Nature Portfolio
2016
|
Materias: | |
Acceso en línea: | https://doaj.org/article/64c4b3b1f151448da9dc8c818a6f3f7e |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
Ejemplares similares
-
FRET-enhanced photostability allows improved single-molecule tracking of proteins and protein complexes in live mammalian cells
por: Srinjan Basu, et al.
Publicado: (2018) -
Simultaneous live cell imaging using dual FRET sensors with a single excitation light.
por: Yusuke Niino, et al.
Publicado: (2009) -
Structural resolution of inorganic nanotubes with complex stoichiometry
por: Geoffrey Monet, et al.
Publicado: (2018) -
An intermolecular FRET sensor detects the dynamics of T cell receptor clustering
por: Yuanqing Ma, et al.
Publicado: (2017) -
A FRET biosensor reveals spatiotemporal activation and functions of aurora kinase A in living cells
por: Giulia Bertolin, et al.
Publicado: (2016)