Skip to Content
Merck
  • Therapeutic monoclonal antibodies and consistent ends: terminal heterogeneity, detection, and impact on quality.

Therapeutic monoclonal antibodies and consistent ends: terminal heterogeneity, detection, and impact on quality.

Current opinion in biotechnology (2014-07-16)
Kurt Brorson, Audrey Y Jia
ABSTRACT

Monoclonal antibodies (mAbs) are biological macromolecules with complex post-translational modifications that can be observed when assessing product variants. The N- and C-terminal heterogeneities of commercially produced antibodies have been observed and extensively studied over the past 30 years. This review summarizes the current literature on detectable antibody termini variants from cultured cells. The presence of these heterogeneities can be detected by many different analytical methods, mostly based on sequence, charge and size differences. Examples are presented that highlight terminal heterogeneities, methods of detection, and their impact on the quality of mAbs. Regulatory considerations are also discussed regarding the potential impact on product quality, safety, and efficacy.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
L-Glutamic acid, ReagentPlus®, ≥99% (HPLC)
Sigma-Aldrich
L-Glutamic acid, from non-animal source, meets EP testing specifications, suitable for cell culture, 98.5-100.5%
Supelco
L-Glutamic acid, Pharmaceutical Secondary Standard; Certified Reference Material
Supelco
L-Glutamic acid, certified reference material, TraceCERT®, Manufactured by: Sigma-Aldrich Production GmbH, Switzerland
Sigma-Aldrich
D-Glutamic acid, ≥99% (TLC)
Sigma-Aldrich
L-Glutamic acid, FCC
Sigma-Aldrich
L-Glutamic acid, BioUltra, ≥99.5% (NT)
Pidolic acid, European Pharmacopoeia (EP) Reference Standard
Glutamic acid, European Pharmacopoeia (EP) Reference Standard
Sigma-Aldrich
L-Glutamic acid hydrochloride, ≥99% (HPLC)
Sigma-Aldrich
L-Pyroglutamic acid, BioXtra
Sigma-Aldrich
L-Pyroglutamic acid, ≥99.0% (T)