Wikipedia

Nano differential scanning fluorimetry

NanoDSF is a type of differential scanning fluorimetry (DSF) method used to determine conformational protein stability by employing intrinsic tryptophan or tyrosine fluorescence, as opposed to the use of extrinsic fluorogenic dyes that are typically monitored via a qPCR instrument.[1] A nanoDSF assay is also known as a type of Thermal Shift Assay.

Thermal unfolding curves and unfolding transition midpoints of two monoclonal antibodies. (A) Thermal unfolding curves of two monoclonal antibodies in the presence of 25 mM Na-Citrate at different pH values. Insets show the pH-dependence of the first unfolding midpoint (Tm1). (B) Dependence of Tm1 and Tm2 on the pH of the buffer of all tested conditions.

Protein stability is typically addressed by thermal or chemical unfolding experiments.[2] In thermal unfolding experiments, a linear temperature ramp is applied to unfold proteins, whereas chemical unfolding experiments use chemical denaturants in increasing concentrations. The thermal stability of a protein is typically described by the 'melting temperature' or 'Tm', at which 50% of the protein population is unfolded, corresponding to the midpoint of the transition from folded to unfolded.

In contrast to conventional DSF methods, nanoDSF uses tryptophan or tyrosine fluorescence to monitor protein unfolding. Both the fluorescence intensity and the fluorescence maximum strongly depend on the close chemical environment of the tryptophan.[3] Typically, interior tryptophan residues in a more hydrophobic environment exhibit a notable emission red shift from approximately 330 nm to 350 nm upon protein unfolding and exposure to water. Quantification of these fluorescence wavelength shifts at various temperature intervals yields a measurement of Tm. Accepted methods to detect and quantify the fluorescence wavelength shift include measuring the intensity at a single wavelength, computing a ratio of the intensity at two wavelengths (typically 330 nm and 350 nm), or calculating the barycentric mean (BCM) by measuring the center of mass of the fluorescence waveform. The latter BCM method takes advantage of the entire UV-fluorescence spectrum, thus allowing for flexibility when auto-fluorescent small molecules are present.

Applications of nanoDSF include protein or antibody engineering, membrane protein research, quality control and formulation development, and ligand binding.[4][5][6][7] NanoDSF has also been utilized to rapidly evaluate the melting points of enzyme libraries for biotechnological applications.[8]

Currently there are at least three instruments on the market that can measure fluorescence wavelength shifts in a high-throughput manner while heating the samples through a defined temperature ramp. These instruments employ either proprietary capillaries[9][10] or generic high-throughput 384-well plates[11] for sample analysis.

Applications

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The nanoDSF technology was used to confirm on-target binding of BI-3231 to HSD17B13 and to elucidate its uncompetitive mode of inhibition with regards to NAD+.[12]

NanoDSF was used to compare the thermal stability of a matched set of anti-CD20 antibodies representing a range of variants. The results revealed a spectrum of activities.[13]

References

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  1. ^ Gao K, Oerlemans R, Groves MR (February 2020). "Theory and applications of differential scanning fluorimetry in early-stage drug discovery". Biophysical Reviews. 12 (1): 85–104. doi:10.1007/s12551-020-00619-2. PMC 7040159. PMID 32006251.
  2. ^ Senisterra G, Chau I, Vedadi M (April 2012). "Thermal denaturation assays in chemical biology". Assay and Drug Development Technologies. 10 (2): 128–36. doi:10.1089/adt.2011.0390. PMID 22066913.
  3. ^ Lakowicz JR (2006). Principles of Fluorescence Spectroscopy (3rd ed.). Springer US. ISBN 978-0-387-31278-1.
  4. ^ Wen J, Lord H, Knutson N, Wikström M (March 2020). "Nano differential scanning fluorimetry for comparability studies of therapeutic proteins". Analytical Biochemistry. 593: 113581. doi:10.1016/j.ab.2020.113581. PMID 31935356.
  5. ^ "App Notes". Unchained Labs.
  6. ^ "Differential Scanning Fluorimetry Application Notes". Applied Photophysics. Retrieved 2024-10-11.
  7. ^ Vivoli M, Novak HR, Littlechild JA, Harmer NJ (September 2014). "Determination of protein-ligand interactions using differential scanning fluorimetry". Journal of Visualized Experiments (91): 51809. doi:10.3791/51809. PMC 4692391. PMID 25285605.
  8. ^ Magnusson AO, Szekrenyi A, Joosten HJ, Finnigan J, Charnock S, Fessner WD (January 2019). "nanoDSF as screening tool for enzyme libraries and biotechnology development". The FEBS Journal. 286 (1): 184–204. doi:10.1111/febs.14696. PMC 7379660. PMID 30414312.
  9. ^ "nanoDSF". NanoTemper Technologies. Retrieved 2024-10-11.
  10. ^ "Uncle - Protein Stability Screening Platform | Unchained Labs". unchainedlabs. Retrieved 2024-10-11.
  11. ^ "SUPR-DSF". Applied Photophysics. Retrieved 2024-10-11.
  12. ^ Thamm S, Willwacher MK, Aspnes GE, Bretschneider T, Brown NF, Buschbom-Helmke S, et al. (February 2023). "Discovery of a Novel Potent and Selective HSD17B13 Inhibitor, BI-3231, a Well-Characterized Chemical Probe Available for Open Science". Journal of Medicinal Chemistry. 66 (4): 2832–2850. doi:10.1021/acs.jmedchem.2c01884. PMC 9969402. PMID 36727857.
  13. ^ Hale G, Davy AD, Wilkinson I (2024-12-31). "Systematic analysis of Fc mutations designed to enhance binding to Fc-gamma receptors". mAbs. 16 (1): 2406539. doi:10.1080/19420862.2024.2406539. PMC 11418285. PMID 39306747.

Further reading

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