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In meso crystallogenesis. Compatibility of the lipid cubic phase with the synthetic digitonin analogue, glyco‐diosgenin
Ist Teil von
Journal of applied crystallography, 2020-04, Vol.53 (2), p.530-535
Ort / Verlag
5 Abbey Square, Chester, Cheshire CH1 2HU, England: International Union of Crystallography
Erscheinungsjahr
2020
Link zum Volltext
Quelle
Wiley-Blackwell Full Collection
Beschreibungen/Notizen
Digitonin has long been used as a mild detergent for extracting proteins from membranes for structure and function studies. As supplied commercially, digitonin is inhomogeneous and requires lengthy pre‐treatment for reliable downstream use. Glyco‐diosgenin (GDN) is a recently introduced synthetic surfactant with features that mimic digitonin. It is available in homogeneously pure form. GDN is proving to be a useful detergent, particularly in the area of single‐particle cryo‐electron microscopic studies of membrane integral proteins. With a view to using it as a detergent for crystallization trials by the in meso or lipid cubic phase method, it was important to establish the carrying capacity of the cubic mesophase for GDN. This was quantified in the current study using small‐angle X‐ray scattering for mesophase identification and phase microstructure characterization as a function of temperature and GDN concentration. The data show that the lipid cubic phase formed by hydrated monoolein tolerates GDN to concentrations orders of magnitude in excess of those used for membrane protein studies. Thus, having GDN in a typical membrane protein preparation should not deter use of the in meso method for crystallogenesis.
The lipid cubic phase is compatible with the synthetic digitonin analogue, GDN, over a considerable range of concentrations, indeed well beyond those likely to be encountered in typical membrane crystallization studies. Thus, based on its compatibility with the cubic phase, there is every reason to use GDN as a detergent for preparing membrane proteins that are subsequently subjected to in meso crystallogenesis.