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| Protein and Antibody Isolation> | the supernatant of cell lysates clarified by centrifugation (8184 x g, 1 h) was then affinity purified using Pierce™ anti-DYKDDDDK affinity resin (ThermoFisher Scientific, A36801) and eluted with 3 x Flag peptide (GenScript, RP21087), concentrated using an Amicon™ Ultra-4 centrifugal filter (Sigma-Aldrich, UFC805024), analyzed by SDS-PAGE, aliquoted and flash frozen. | Get A Quote |
Membrane scaffold protein-based nanodiscs have facilitated unprecedented structural and biophysical analysis of membrane proteins in a near-native lipid environment. However, successful reconstitution of membrane proteins in nanodiscs requires prior solubilization and purification in detergents, which may impact their physiological structure and function. Furthermore, the detergent-mediated reconstitution of nanodiscs is unlikely to recapitulate the precise composition or asymmetry of native membranes. To circumvent this fundamental limitation of traditional nanodisc technology, we herein describe the development of membrane-solubilizing peptides to directly extract membrane proteins from native cell membranes ... More