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High-Throughput Assessment of Structural Continuity in Biologics

[Image: see text] We demonstrate a high-throughput chemoprinting platform that confirms the consistency in the higher-order structure of protein biologics and is sensitive enough to detect single-point mutations. This method addresses the quality and consistency of the tertiary and quaternary struct...

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Detalles Bibliográficos
Autores principales: Musetti, Caterina, Bean, Mark F., Quinque, Geoffrey T., Kwiatkowski, Christopher, Szewczuk, Lawrence M., Baldoni, John, Zajac, Matthew A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2018
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6349355/
https://www.ncbi.nlm.nih.gov/pubmed/29369625
http://dx.doi.org/10.1021/acs.analchem.8b00180
Descripción
Sumario:[Image: see text] We demonstrate a high-throughput chemoprinting platform that confirms the consistency in the higher-order structure of protein biologics and is sensitive enough to detect single-point mutations. This method addresses the quality and consistency of the tertiary and quaternary structure of biologic drug products, which is arguably the most important, yet rarely examined, parameter. The method described uses specific small-molecule ligands as molecular probes to assess protein structure. Each library of probe molecules provides a “fingerprint” when taken holistically. After proof-of-concept experiments involving enzymes and antibodies, we were able to detect minor conformational perturbations between four 48 kDa protein mutants that only differ by one amino acid residue.