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The biologics researcher's mini-guide to screening candidates with nanoDSF

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Antibody Engineering There are various approaches to creating new antibody therapeutics. Generally, you start with a mAb that had already proven effective at targeting and binding a protein of interest, and work with it as a starting point to improve its stability and affinity to make it a more effective therapeutic. Optimizing this parent molecule with random mutations, rationally-designed mutations, or mutations directed from computer models improves the developability of your therapeutic mAb. However, even a single point mutation offers the potential for a BIG impact on your candidate's stability — both for the better, and for the worse. It's critical to check what impact protein engineering has on your candidate molecule's stability. With high-resolution nanoDSF data, it becomes clear how just a few point mutations have an impact on T m values — increasing or decreasing stability by a few degrees.

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