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DeFrND: detergent-free reconstitution into native nanodiscs with designer membrane scaffold peptides

Nature Communications. 2025-08; 
Qian Ren, Jing Wang, Vinay Idikuda, Shanwen Zhang, Jeehae Shin, W Grant Ludlam, Luis M Real Hernandez, Sara Zdancewicz, Alex J B Kreutzberger, Hucheng Chang, Volker Kiessling, Lukas K Tamm, Ahmad Jomaa, Ilya Levental, Kirill Martemyanov, Baron Chanda, Huan Bao, Dhanya Thamaraparambil Jayaram, Pranav Sivaram, Pranjal Biswas, Yue Dai, Elizabeth A Sweeny, Dennis J Stuehr Department of Molecular Medicine, UF Scripps Biomedical Research, Jupiter
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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

Abstract

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

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