Application Notes

Prometheus: the platform for analyzing protein stability and thermal unfolding of proteins

Issue link: https://resources.nanotempertech.com/i/1050485

Contents of this Issue

Navigation

Page 5 of 9

6 APPLICATION NOTE ©2017 NanoTemper Technologies, Inc. South San Francisco, CA, USA. All Rights Reserved. the use of Prometheus capillaries offers an even higher precision for UV-fluorescence detection than high-performance quartz-cuvettes, with the additional benefit of low sample consumption, high-throughput and high versatility. Moreover, the capillary-based approach prevents cross-contamination, and no laborious and time-consuming cleaning steps are required. High scanning rates and thus high data density moreover allow for a robust analysis of melting curves, and also enables a precise determination of unfolding onsets. In addition, the direct detection of tryptophan fluorescence to monitor protein unfolding has several benefits compared to other methods routinely used to monitor thermal unfolding, such as differential scanning fluorimetry (DSF) or thermofluor assays. These assays use external fluorophores which bind to hydrophobic patches of the protein usually buried in the core of the protein. Upon unfolding, these patches get exposed and the fluorophore attaches, resulting in an increase in fluorescence. These assays, however, are not suited for a detailed analysis of folding thermodynamics, since they interfere with folding-unfolding equilibria by directly interacting with the proteins. Moreover, the external fluorophores are incompatible with a number of buffers (e.g. including detergents) or protein types, such as membrane proteins. Lastly, although DSF is routinely used in primary screenings in the drug discovery process, external fluorophores can interact with compounds or block binding sites and produce false-negative as well as false-positive results. In addition to its capabilities in monitoring thermal unfolding of a large number of samples in parallel, the Prometheus can also be used to analyze chemical Figure 4: Ca 2+ effects on amylase stability. Removal of Ca 2+ ions results in a marked destabilization of both amylase isoforms, as indicated by the shi of T m towards lower values. Pig pancreatic α-amylase PPA Aspergillus orzae α-amylase TAKA Temp (°C) Temp (°C)

Articles in this issue

view archives of Application Notes - Prometheus: the platform for analyzing protein stability and thermal unfolding of proteins