Cargando…
Site-specific fluorescent labeling to visualize membrane translocation of a myristoyl switch protein
Fluorescence approaches have been widely used for elucidating the dynamics of protein-membrane interactions in cells and model systems. However, non-specific multi-site fluorescent labeling often results in a loss of native structure and function, and single cysteine labeling is not feasible when na...
Autores principales: | Yang, Sung-Tae, Lim, Sung In, Kiessling, Volker, Kwon, Inchan, Tamm, Lukas K. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5015116/ https://www.ncbi.nlm.nih.gov/pubmed/27605302 http://dx.doi.org/10.1038/srep32866 |
Ejemplares similares
-
Planar Supported Membranes with Mobile SNARE Proteins and Quantitative Fluorescence Microscopy Assays to Study Synaptic Vesicle Fusion
por: Kiessling, Volker, et al.
Publicado: (2017) -
Line tension at lipid phase boundaries as driving force for HIV fusion peptide-mediated fusion
por: Yang, Sung-Tae, et al.
Publicado: (2016) -
HIV gp41-Mediated Membrane Fusion Occurs at Edges of Cholesterol-Rich Lipid Domains
por: Yang, Sung-Tae, et al.
Publicado: (2015) -
Conformational regulation and target-myristoyl switch of calcineurin B homologous protein 3
por: Becker, Florian, et al.
Publicado: (2023) -
HIV virions sense plasma membrane heterogeneity for cell entry
por: Yang, Sung-Tae, et al.
Publicado: (2017)