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Nanodisc-Tm: Rapid functional assessment of nanodisc reconstituted membrane proteins by CPM assay
- Source :
- MethodsX
- Publication Year :
- 2016
- Publisher :
- Elsevier BV, 2016.
-
Abstract
- Graphical abstract<br />Membrane proteins are generally unstable in detergents. Therefore, biochemical and biophysical studies of membrane proteins in lipidic environments provides a near native-like environment suitable for membrane proteins. However, manipulation of proteins embedded in lipid bilayer has remained difficult. Methods such as nanodiscs and lipid cubic phase have been developed for easy manipulation of membrane proteins and have yielded significant insights into membrane proteins. Traditionally functional reconstitution of receptors in nanodiscs has been studied with radioligands. We present a simple and faster method for studying the functionality of reconstituted membrane proteins for routine characterization of protein batches after initial optimization of suitable conditions using radioligands. The benefits of the method are • Faster and generic method to assess functional reconstitution of membrane proteins. • Adaptable in high throughput format (≥96 well format). • Stability measurement in near-native lipid environment and lipid dependent melting temperatures.
- Subjects :
- 0301 basic medicine
Chemistry
Clinical Biochemistry
Nanodiscs
Nanotechnology
03 medical and health sciences
Medical Laboratory Technology
CPM assay
030104 developmental biology
Membrane
Membrane protein
Biochemistry, Genetics and Molecular Biology
Nanodisc-Tm
Membrane proteins
Biophysics
lipids (amino acids, peptides, and proteins)
Lipid bilayer
Receptor
Nanodisc
ComputingMethodologies_COMPUTERGRAPHICS
Subjects
Details
- ISSN :
- 22150161
- Volume :
- 3
- Database :
- OpenAIRE
- Journal :
- MethodsX
- Accession number :
- edsair.doi.dedup.....a722e044d73fa84e55760b6b6d67b26e
- Full Text :
- https://doi.org/10.1016/j.mex.2016.03.009