Protein Thermal Shift™ Software & Reagents
Protein Thermal Shift™ solution for differential scanning fluorometry
Applied Biosystems® Protein Thermal Shift™ Software and reagent kits, plus real-time PCR systems, offer high-throughput protein melt analysis that requires <1 µg of sample per well, at a cost that is significantly lower than alternative methods.
Life Technologies™ Protein Thermal Shift™ Software and reagent kits, plus real-time PCR systems, offer high-throughput protein melt analysis that requires <1 µg of sample per well, at a cost that is significantly lower than alternative methods.
Proteins are typically key target molecules studied during the drug development process. The high-throughput screening of small molecule and ligand libraries that bind to protein targets is often an important and time-consuming part of the process—requiring the screening of thousands of samples with a variety of assays over a period of months. However, since protein targets can be challenging to work with due to their susceptibility to degradation and aggregation, protein stability screening is often an important component of lead-generation programs.
Protein stability screening can be performed using the protein melting method often employed in research programs that study native proteins. Protein melting is useful for identifying ligand and buffer conditions that maximize the stability of proteins during purification, crystallization, and functional characterization.
Historically, protein melt screening methods have been inefficient or expensive, either capable of analyzing only one sample at a time, or confined to high-throughput methods that required milligram quantities of protein sample and incurred high reagent costs. Our Protein Thermal Shift™ Software and reagent kits offer an economical and efficient protein method for melt analysis, with the capability of high-throughput analysis using very small sample quantities to identify ligands, mutations, modifications, and buffer conditions that increase their Tm and relative stability. They can also be used to screen antibody–ligand binding as part of the antibody optimization process.
Protein stability changes with buffer pH, salt content, and the presence of various co-factors in storage or reaction buffers. Real-time melt experiments that use protein-binding dyes, such as PTS, and our real-time PCR systems, yield a fluorescence profile that is specific to the protein of interest in a given test buffer environment. Variations in pH, salt content, or test buffer components appear as changes in this fluorescence profile (melt curve). This is converted to a Tm which is calculated based on the inflection point of the melt curve.
- Mix protein, buffer, ligand (if applicable), and PTS dye
- Run a melt-curve experiment on a real-time PCR instrument
- The protein unfolds as it is heated
- The environmentally-sensitive PTS dye binds exposed hydrophobic regions and fluoresces
- The melting temperature (Tm) is calculated from the melt curve
- Changes in Tm are correlated to changes in protein stability or ligand binding
Protein Stability Screening:
High-Throughput Ligand Screening:
- User Guide: Protein Thermal Shift™ Studies
- Application Note: Protein Thermal Shift™ Studies
- Product Bulletin: Protein Thermal Shift™ Studies
- Protein Thermal Shift™ Data Sheet
- Protein Thermal Shift™ Studies Buffer Screening Quick Reference
- Protein Thermal Shift™ Studies Mutation Screening Quick Reference
- Protein Thermal Shift™ Studies Ligand Screening Quick Reference
- Poster: Protein Thermal Shift Assay is an Excellent High Throughput Screening Strategy To Identify Optimal Buffer Conditions And Ligands Required For Maximizing YraM Protein Crystallization Success
- Real-time PCR technology measures the effect of compound binding on protein stability
- Use of Protein Thermal Shift™ technology in design of novel antibodies for cancer research
Protein Thermal Shift™ (PTS) reagents enable protein melt assays that can be used as an efficient screening tool for measuring protein thermal stability, identifying suitable buffer conditions, and measuring protein–ligand interactions. The assay is very easy to set up and run, with typical time-to-results of 0.5–2 hours, depending on the real-time system and assay conditions.