High resolution separation of recombinant monoclonal antibodies by size-exclusion ultra-high performance liquid chromatography (SE-UHPLC).

J Pharm Biomed Anal

Department of Protein Analytical Chemistry, Genentech Inc., 1 DNA Way, South San Francisco, CA 94080, USA. Electronic address:

Published: May 2015

Size-exclusion chromatography (SEC) is an important mode of separation used in monoclonal antibody (mAb) characterization and quality control. SEC separates mAbs into three major species: high molecular weight species, main peak (predominantly monomer), and low molecular weight species. However, mAb SEC separations have low resolution between the different sized species, and the analysis is slow with low sample throughput. The introduction of size-exclusion ultra-high performance liquid chromatography (SE-UHPLC) columns offers a new opportunity to improve both the resolution and throughput of SEC analysis. This study demonstrates that SE-UHPLC columns deliver better resolution of size variants in a shorter period of time than conventional SEC columns. For example, an SE-UHPLC column 300-mm in length produced separation of mAb Fab/c fragments in less than 10min, in comparison to a conventional SEC column output, where these fragments co-elute with the main peak. Furthermore, we observed that high back pressure does not generate HMWS under optimized mobile phase conditions for mAbs. The platform SE-UHPLC method has been demonstrated to be suitable for the analysis of multiple mAbs, with greatly improved sample throughput and peak resolution of mAb size variants.

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.jpba.2015.02.032DOI Listing

Publication Analysis

Top Keywords

size-exclusion ultra-high
8
ultra-high performance
8
performance liquid
8
liquid chromatography
8
chromatography se-uhplc
8
molecular weight
8
weight species
8
main peak
8
sample throughput
8
se-uhplc columns
8

Similar Publications

Study of humic-like substances of dissolved organic matter using size exclusion chromatography and chemometrics.

J Environ Manage

August 2024

Laboratoire SOFTMAT (IMRCP), Université de Toulouse, CNRS UMR 5623, Université Paul Sabatier, 118 route de Narbonne, CEDEX 9, 31062, Toulouse, France. Electronic address:

Article Synopsis
  • The study focuses on the analysis of dissolved organic matter (DOM) in wastewater treatment, specifically targeting recalcitrant compounds that arise from thermal sludge pretreatment.
  • Researchers developed a method using ultra-high-performance liquid chromatography size-exclusion chromatography (U-HPLC SEC) combined with UV and fluorescence detection to differentiate between melanoidins and humic acids (HAs).
  • The findings show that low molecular weight fractions indicate melanoidins, while high molecular weight fractions are characteristic of HAs, and specific detection modes yield distinct fluorescence patterns relevant in classifying these organic compounds.
View Article and Find Full Text PDF

Slalom chromatography (SC) was discovered in 1988 for analyzing double-stranded (ds) DNA. However, its progress was impeded by practical issues such as low-purity particles, sample loss, and lack of a clear retention mechanism. With the rise of cell and gene therapies and the availability today of bio-inert ultra-high-pressure liquid chromatography (UHPLC) columns and systems, SC has regained interest.

View Article and Find Full Text PDF

The technical difficulty of separating extracellular vesicles (EVs) from plasma proteins in human blood presents a significant hurdle in EV research, particularly during nano ultra-high-performance liquid chromatography-tandem mass spectrometric (UHPLC-MS/MS) analysis, where detecting "vesicular" proteins among abundant plasma proteins is challenging. Standardisation is a pressing issue in EV research, prompting collaborative global efforts to address it. While the MISEV guidelines offer valuable recommendations, unanswered questions remain, particularly regarding sample storage.

View Article and Find Full Text PDF

The thorough characterization of chitosan-cleaving enzymes is crucial to unveil structure-function relationships of this promising class of biomolecules for both, enzymatic fingerprinting analyses and to use the enzymes as biotechnological tools to produce tailor-made chitosans for diverse applications. Analyzing polymeric substrates as well as oligomeric products has been established as an effective way to understand the actions of enzymes, but it currently requires separate, rather laborious methods to obtain the full picture. Here, we present ultra high performance size exclusion chromatography coupled to refractive index and mass spectrometry detection (UHPSEC-RI-MS) as a straightforward method for the semi-quantitative analysis of chitosan oligomers of up to ten monomers in length.

View Article and Find Full Text PDF

Physical origin of the peak tailing of monoclonal antibodies in size-exclusion chromatography using bio-compatible systems and columns.

Anal Bioanal Chem

February 2024

Waters Corporation, Instrument/Core Research/Fundamental, Milford, MA, 01757, USA.

The analysis of mixtures containing monoclonal antibody (mAb) (approximately 150 kDa molecular weight) and sub-unit impurities (approximately 100 kDa) is challenging, even when adopting the latest ultra-high-pressure liquid chromatography (UHPLC) columns (4.6 mm [Formula: see text] 150 mm coated hardware, 1.7 [Formula: see text]m 250 BEH[Formula: see text] Surface-modified Particles) and systems (ACQUITY[Formula: see text] UPLC[Formula: see text] I-class Bio Plus).

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!