Cargando…
Von Willebrand factor A1 domain stability and affinity for GPIbα are differentially regulated by its O-glycosylated N- and C-linker
Hemostasis in the arterial circulation is mediated by binding of the A1 domain of the ultralong protein von Willebrand factor (VWF) to GPIbα on platelets to form a platelet plug. A1 is activated by tensile force on VWF concatemers imparted by hydrodynamic drag force. The A1 core is protected from fo...
Autores principales: | Bonazza, Klaus, Iacob, Roxana E, Hudson, Nathan E, Li, Jing, Lu, Chafen, Engen, John R, Springer, Timothy A |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9084892/ https://www.ncbi.nlm.nih.gov/pubmed/35532124 http://dx.doi.org/10.7554/eLife.75760 |
Ejemplares similares
-
The impact of aberrant von Willebrand factor-GPIbα interaction on megakaryopoiesis and platelets in humanized type 2B von Willebrand disease model mouse
por: Kanaji, Sachiko, et al.
Publicado: (2022) -
von Willebrand factor promotes platelet-induced metastasis of osteosarcoma through activation of the VWF-GPIb axis
por: Wang, Q., et al.
Publicado: (2020) -
A novel SH2 recognition mechanism recruits Spt6 to the doubly phosphorylated RNA polymerase II linker at sites of transcription
por: Sdano, Matthew A, et al.
Publicado: (2017) -
Nuclear microenvironments modulate transcription from low-affinity enhancers
por: Tsai, Albert, et al.
Publicado: (2017) -
Pore mutation N617D in the skeletal muscle DHPR blocks Ca(2+) influx due to atypical high-affinity Ca(2+) binding
por: Dayal, Anamika, et al.
Publicado: (2021)