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Christopher Yu

Researcher at Genentech

Publications -  8
Citations -  193

Christopher Yu is an academic researcher from Genentech. The author has contributed to research in topics: Chemistry & Quality (philosophy). The author has an hindex of 5, co-authored 6 publications receiving 116 citations.

Papers
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Journal ArticleDOI

A View on the Importance of “Multi-Attribute Method” for Measuring Purity of Biopharmaceuticals and Improving Overall Control Strategy

TL;DR: A liquid chromatography-mass spectrometry (LC-MS) multi-attribute method (MAM) has been developed and designed for improved simultaneous detection, identification, quantitation, and quality control (monitoring) of molecular attributes.
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Investigating interactions between phospholipase B-Like 2 and antibodies during Protein A chromatography.

TL;DR: The results showed that the co-elution of PLBL2 during Protein A chromatography is highly dependent on the individual antibody andPLBL2 concentration in the chromatographic load, and there is a preference for PLBL 2 to interact with IgG4 subclass antibodies compared to IgG1 antibodies.
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Evaluation of Heavy-Chain C-Terminal Deletion on Product Quality and Pharmacokinetics of Monoclonal Antibodies

TL;DR: This study provides a possible solution to mitigate mAb heterogeneity in C-terminal processing, improve batch-to-batch consistency, and facilitate the comparability study during process changes.
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Multi-attribute method performance profile for quality control of monoclonal antibody therapeutics.

TL;DR: In this article, a multi-attribute method (MAM) using peptide map analysis with high resolution mass spectrometry is used for product characterization and the identification of critical quality attributes (CQAs) of biotherapeutic proteins.
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Evaluation of Heavy Chain C-terminal Deletions on Productivity and Product Quality of Monoclonal Antibodies in Chinese Hamster Ovary (CHO) Cells.

TL;DR: While no measurable differences in antibody HC and LC mRNA levels, glycosylation and secretion were observed, the analysis suggests that the lower specific productivity of clones expressing antibody lacking HC C‐terminal lysine was due to slower antibody HC synthesis and faster antibody degradation.