Time-Dependent Fluorescence Spectroscopy to Quantify Complex Binding Interactions

[Image: see text] Measuring the binding affinity for proteins that can aggregate or undergo complex binding motifs presents a variety of challenges. In this study, fluorescence lifetime measurements using intrinsic tryptophan fluorescence were performed to address these challenges and to quantify th...

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Detalles Bibliográficos
Autores principales: Bernhard, Samuel P., Goodman, Candace K., Norton, Erienne G., Alme, Daniel G., Lawrence, C. Martin, Cloninger, Mary J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2020
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7675582/
https://www.ncbi.nlm.nih.gov/pubmed/33225133
http://dx.doi.org/10.1021/acsomega.0c03416

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7675582/
https://www.ncbi.nlm.nih.gov/pubmed/33225133
http://dx.doi.org/10.1021/acsomega.0c03416

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