Cargando…
Combining biophysical methods for the analysis of protein complex stoichiometry and affinity in SEDPHAT
Reversible macromolecular interactions are ubiquitous in signal transduction pathways, often forming dynamic multi-protein complexes with three or more components. Multivalent binding and cooperativity in these complexes are often key motifs of their biological mechanisms. Traditional solution bioph...
Autores principales: | Zhao, Huaying, Schuck, Peter |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4304681/ https://www.ncbi.nlm.nih.gov/pubmed/25615855 http://dx.doi.org/10.1107/S1399004714010372 |
Ejemplares similares
-
Monochromatic multicomponent fluorescence sedimentation velocity for the study of high-affinity protein interactions
por: Zhao, Huaying, et al.
Publicado: (2016) -
The biophysics of disordered proteins from the point of view of single-molecule fluorescence spectroscopy
por: Cubuk, Jasmine, et al.
Publicado: (2022) -
A Method to Quantify FRET Stoichiometry with Phasor Plot Analysis and Acceptor Lifetime Ingrowth
por: Chen, WeiYue, et al.
Publicado: (2015) -
Isolation and Biophysical Study of Fruit Cuticles
por: Chatterjee, Subhasish, et al.
Publicado: (2012) -
Structure of mouse protocadherin 15 of the stereocilia tip link in complex with LHFPL5
por: Ge, Jingpeng, et al.
Publicado: (2018)