Chattopadhyay, Gopinath and Varadarajan, Raghavan (2019) Facile measurement of protein stability and folding kinetics using a nano differential scanning fluorimeter. In: PROTEIN SCIENCE, 28 (6). pp. 1127-1134.
PDF
Pro_Sci_28_6_1127-1134_2019.pdf - Published Version Restricted to Registered users only Download (1MB) | Request a copy |
Abstract
With advancements in high-throughput generation of phenotypic data on mutant proteins, it has become important to individually characterize different proteins or their variants rapidly and with minimal sample consumption. We have made use of a nano differential scanning fluorimetric device, from NanoTemper technologies, to rapidly carry out isothermal chemical denaturation and measure folding/unfolding kinetics of proteins and compared these to corresponding data obtained from conventional spectrofluorimetry. We show that using sample volumes 10-50-fold lower than with conventional fluorimetric techniques, one can rapidly and accurately measure thermodynamic and kinetic stability, as well as folding/unfolding kinetics. This method also facilitates characterization of proteins that are difficult to express and purify.
Item Type: | Journal Article |
---|---|
Publication: | PROTEIN SCIENCE |
Publisher: | WILEY |
Additional Information: | copyright for this article belongs to PROTEIN SCIENCE |
Keywords: | nano differential scanning fluorimeter; isothermal denaturation; thermodynamic stability; refolding unfolding kinetics |
Department/Centre: | Division of Biological Sciences > Molecular Biophysics Unit |
Date Deposited: | 27 Jun 2019 14:23 |
Last Modified: | 27 Jun 2019 14:23 |
URI: | http://eprints.iisc.ac.in/id/eprint/63045 |
Actions (login required)
View Item |