Minimization of artifact protein aggregation using tetradecyl sulfate and hexadecyl sulfate in capillary gel electrophoresis under reducing conditions.


Journal

Electrophoresis
ISSN: 1522-2683
Titre abrégé: Electrophoresis
Pays: Germany
ID NLM: 8204476

Informations de publication

Date de publication:
07 2020
Historique:
received: 26 11 2019
revised: 31 03 2020
accepted: 01 04 2020
pubmed: 17 4 2020
medline: 23 3 2021
entrez: 17 4 2020
Statut: ppublish

Résumé

In the biopharmaceutical industry, CE-SDS assesses the purity, heterogeneity, and stability of therapeutic proteins. However, for mAb-1 and mAb-2, typical CE-SDS under reducing conditions produced atypical protein peak profiles, which led to biased purity results, thus were not acceptable for biologics manufacturing. This bias was caused by the formation of method-induced higher molecular weight artifacts, the levels of which correlated with protein concentration. Here we show that adding sodium tetradecyl and hexadecyl sulfates to the sample and the sieving gel buffer solutions was required to prevent formation of aggregate artifacts and to maintain detergent:protein uniformity, suggesting their importance during the sample preparation steps of heat denaturation and subsequent cooling as well as during capillary migration. For these proteins, we show that this uniformity was likely due to the ability of these detergents to bind proteins with markedly higher affinities compared to SDS. "CE-SC

Identifiants

pubmed: 32297333
doi: 10.1002/elps.201900435
doi:

Substances chimiques

Antibodies, Monoclonal 0
Detergents 0
Protein Aggregates 0
Proteins 0
Sodium Tetradecyl Sulfate Q1SUG5KBD6

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1245-1252

Informations de copyright

© 2020 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

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Auteurs

Qian Guan (Q)

Biologics Development, Bristol-Myers Squibb Company, 38 Jackson Road, Devens, MA, 01434, USA.

Jennifer Atsma (J)

Biologics Development, Bristol-Myers Squibb Company, 38 Jackson Road, Devens, MA, 01434, USA.

Rekha Tulsan (R)

Biologics Development, Bristol-Myers Squibb Company, 38 Jackson Road, Devens, MA, 01434, USA.

Sergey Voronov (S)

Biologics Development, Bristol-Myers Squibb Company, 38 Jackson Road, Devens, MA, 01434, USA.

Julia Ding (J)

Biologics Development, Bristol-Myers Squibb Company, 38 Jackson Road, Devens, MA, 01434, USA.

Jeff Beckman (J)

Biologics Development, Bristol-Myers Squibb Company, 38 Jackson Road, Devens, MA, 01434, USA.

Zheng Jian Li (ZJ)

Biologics Development, Bristol-Myers Squibb Company, 38 Jackson Road, Devens, MA, 01434, USA.

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Classifications MeSH