Jeggle P, Smith ESJ, Stewart AP, Härteis S, Korbmacher C, Edwardson JM (2015)
Publication Type: Journal article
Publication year: 2015
Book Volume: 464
Pages Range: 38-44
Journal Issue: 1
DOI: 10.1016/j.bbrc.2015.05.091
ASIC and ENaC are co-expressed in various cell types, and there is evidence for a close association between them. Here, we used atomic force microscopy (AFM) to determine whether ASIC1a and ENaC subunits are able to form cross-clade hybrid ion channels. ASIC1a and ENaC could be co-isolated from detergent extracts of tsA 201 cells co-expressing the two subunits. Isolated proteins were incubated with antibodies against ENaC and Fab fragments against ASIC1a. AFM imaging revealed proteins that were decorated by both an antibody and a Fab fragment with an angle of ~120° between them, indicating the formation of ASIC1a/ENaC heterotrimers.
APA:
Jeggle, P., Smith, E.S.J., Stewart, A.P., Härteis, S., Korbmacher, C., & Edwardson, J.M. (2015). Atomic force microscopy imaging reveals the formation of ASIC/ENaC cross-clade ion channels. Biochemical and Biophysical Research Communications, 464(1), 38-44. https://doi.org/10.1016/j.bbrc.2015.05.091
MLA:
Jeggle, Pia, et al. "Atomic force microscopy imaging reveals the formation of ASIC/ENaC cross-clade ion channels." Biochemical and Biophysical Research Communications 464.1 (2015): 38-44.
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