Nano differential scanning fluorimetry (nanoDSF / nDSF)

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Nano differential scanning fluorimetry (nanoDSF / nDSF) is a fast and low-volume technique to determine melting temperatures of proteins using their intrinsic florescence.

NanoDSF Nanotemper nDSF

In nanoDSF, a protein in solution is exposed to a temperature gradient that will lead to the unfolding of the protein. The intrinsic fluorescence of the protein, mainly originating from the aromatic side-chains of tyrosine and tryptophan residues, is examined. Upon unfolding, the environment of those residues will alter because they become exposed to the solvent and thus, their fluorescence intensity will change. The relation between fluorescence intensity changes and temperature gradient can be used to obtain a so-called apparent melting temperature (Tm). Also, information can be gained indicating cooperative (two-state) or complex unfolding transitions in multi-domain proteins. The melting temperature is called “apparent” because its value may differ from the Tm obtained by differential scanning calorimetry (µDSC), since a 50% unfolding state does not necessarily correlate to a 50% change in intrinsic fluorescence signal.

Using nanoDSF to determine the conformational stability of proteins.

nanoDSF capillaries

nanoDSF allows rapid analysis of multiple samples in parallel under identical conditions, e.g., within a formulation development study using different stabilizing excipients, thus being a valuable tool for formulation screening studies.

Besides the small sample volumes required (as low as 10 µL), nanoDSF offers much shorter analysis times and is easier to set up than DSC. nanoDSF is thus a highly valuable alternative to µDSC, particularly in early research and development.

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Breitsprecher D., Glücklich N., Hawe A., Menzen T. "nanoDSF vs. µDSC: A Comparative Study for Biopharmaceutical Formulation Development" Whitepaper 2016

Svilenov HL., Menzen T., Richter K., Winter G. "Modulated Scanning Fluorimetry Can Quickly Assess Thermal Protein Unfolding Reversibility in Microvolume Samples"  Mol Pharm March 2020

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