nanoDSF, the miniaturized differential scanning fluorimetry technology, is a revolutionary method to determine the thermostability of proteins by following changes in their intrinsic fluorescence. In this comparative study, the Prometheus NT.48 was used to determine the thermal stability of the membrane esterase PA2949 from Pseudomonas aeruginosa in presence of various detergents. The detergent type strongly affected enzyme thermal stability, which moreover correlated with enzyme activity. Thus, the Prometheus NT.48 can be used not only to rapidly screen for optimal purification conditions for enzymes, but also to evaluate enzyme activities based on their conformational stability in presence of detergents.
Home
»
Application Notes
»
nanoDSF thermal unfolding analysis of a membrane-bound esterase in various detergents
×
Share
Have a question about Prometheus?
Contact SpecialistMost recent content
How Pierre Fabre Laboratories enhances their antibody developability platform
Learn how Pierre Fabre uses multi-parameter stability measurements of mAb libraries on Prometheus Panta to streamline developability platforms, reducing complexity, cost, and sample consumption.
Optimization of membrane proteins for cryo-EM: Screening of copolymer nanodiscs with Prometheus Panta
Membrane proteins present challenges for structural analysis by cryo-EM; Screening of synthetic copolymers with nanoDSF and DLS on Prometheus Panta help select the best solubilization conditions.
How Merck KGaA uses light scattering measurements for better developability assessment of biologic therapeutics
Biologics developability: learn how Merck uses Prometheus Panta to create developability profiles for their mAbs
Quantifying oligonucleotides binding to human serum albumin with MST: A faster and precise approach for drug candidates ADME profiling
Fast molecular interaction screening of epigenetic gene regulator G9a with fragments from a large chemical space
Rapid Quantification of Unfolded Proteins for Quality Control and Optimization of Storage Conditions
Protein labeling – improved quantitation of biomolecular interactions by MST using the RED-NHS 2nd generation labeling kit
One-step, purification-free and site-specific labeling of polyhistidine-tagged proteins for MST
Anaerobic MicroScale Thermophoresis reveals the redox dependency of ferredoxin in mitochondrial Fe/S biogenesis