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Multiplex measurement of protein–peptide dissociation constants using dialysis and mass spectrometry

We propose a high‐throughput method for quantitatively measuring hundreds of protein–peptide binding affinities in parallel. In this assay, a solution of protein is dialyzed into a buffer containing a pool of potential binding peptides, such that upon equilibration the relative abundance of a peptid...

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Detalles Bibliográficos
Autores principales: Zhao, Yu, Grigoryan, Gevorg
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10031237/
https://www.ncbi.nlm.nih.gov/pubmed/36823715
http://dx.doi.org/10.1002/pro.4607