2012
DOI: 10.1021/ac3008847
|View full text |Cite
|
Sign up to set email alerts
|

Charge Heterogeneity of Monoclonal Antibodies by Multiplexed Imaged Capillary Isoelectric Focusing Immunoassay with Chemiluminescence Detection

Abstract: Characterization of charge heterogeneity of recombinant monoclonal antibodies (mAbs) requires high throughput analytical methods to support clone selection and formulation screens. We applied the NanoPro technology to rapidly measure relative charge distribution of mAbs in early stage process development. The NanoPro is a multiplexed capillary-based isoelectric immunoassay with whole-column imaging detection. This assay offers specificity, speed and sensitivity advantages over conventional capillary isoelectri… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1

Citation Types

0
45
0

Year Published

2013
2013
2017
2017

Publication Types

Select...
10

Relationship

1
9

Authors

Journals

citations
Cited by 45 publications
(45 citation statements)
references
References 21 publications
0
45
0
Order By: Relevance
“…Furthermore, the following analytical methods were applied: Size-exclusion chromatography, non-gel sieving denaturing capillary electrophoresis (CE-SDS; non-reduced and reduced), capillary isoelectric focusing (CE-IEF), reversephase UPLC of released and labeled oligosaccharides, mAb1specific SPR target binding assay and mAb1-specific qualified cell-based functional assay (the latter two assays were developed in-house). [38][39][40][41][42][43][44] The five samples were comparable with regard to quality and physico-chemical properties by using the above mentioned analytical methods, e.g., very low aggregate content, unaltered charge distribution, identical oligosaccharide profiles, in vitro target binding and functionality (data not shown).…”
Section: Physico-chemical and Functional Characterizationmentioning
confidence: 99%
“…Furthermore, the following analytical methods were applied: Size-exclusion chromatography, non-gel sieving denaturing capillary electrophoresis (CE-SDS; non-reduced and reduced), capillary isoelectric focusing (CE-IEF), reversephase UPLC of released and labeled oligosaccharides, mAb1specific SPR target binding assay and mAb1-specific qualified cell-based functional assay (the latter two assays were developed in-house). [38][39][40][41][42][43][44] The five samples were comparable with regard to quality and physico-chemical properties by using the above mentioned analytical methods, e.g., very low aggregate content, unaltered charge distribution, identical oligosaccharide profiles, in vitro target binding and functionality (data not shown).…”
Section: Physico-chemical and Functional Characterizationmentioning
confidence: 99%
“…Capillary Isoelectric Focusing Immunoassay (NanoPro)-Protein samples of gH/gL and gH/gL/pUL128 -131 pentameric complex were analyzed on the ProteinSimple Peggy system (NanoPro) according to manufacturer's instructions with minor modification as previously described (21). Briefly, samples were diluted to the same concentration in Bicine CHAPS buffer (ProteinSimple).…”
Section: Purification Of Gh/gl and Gh/gl/pul128 -131 Pentamericmentioning
confidence: 99%
“…15 However, MS still needs to be used in concomitance with orthogonal analytical techniques to be able to focus on the different facets of the protein including mainly liquid chromatography (LC). [16][17][18][19][20][21][22] Recently, we described a method using capillary zone electrophoresis (CZE) coupled to tandem MS with a sheathless interface to perform the simultaneous characterization of several aspects of a protein in one injection, including AA sequence and posttranslational modifications (PTMs). 23 The sheathless CE-ESI-MS interface, referred to as CESI-MS, has been developed based on an original design proposed by Moini et al 24 Detailed description of this interface has been given by Haselberg et al 25 The CESI system has been used to perform successful CE-ESI-MS experiments in proteomics, 26,27 metabolomics, 28 intact proteins, 25 therapeutic small molecules 29 and as an infusion platform, 30 and it demonstrated a drastically increased sensitivity compared to sheath-liquid CE-MS interfaces because of its low operating flow rates below 100 nL/min.…”
Section: Introductionmentioning
confidence: 99%