## Abstract During the last years native chemical ligation (NCL) gained in popularity as a method allowing the chemical synthesis of large peptides and entire proteins. NCL is particularly well‐suited for chemoselective and nondenaturing attachment of biomolecules on solid substrates. In the presen
At-line monitoring of bioreactor protein production by surface plasmon resonance
✍ Scribed by R. Jacquemart; N. Chavane; Y. Durocher; C. Hoemann; G. De Crescenzo; M. Jolicoeur
- Publisher
- John Wiley and Sons
- Year
- 2008
- Tongue
- English
- Weight
- 139 KB
- Volume
- 100
- Category
- Article
- ISSN
- 0006-3592
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
An innovative and automated method for the at‐line monitoring of secreted protein was developed by harnessing a Surface Plasmon Resonance‐based biosensor to a bioreactor. The proof of concept was performed by following at‐line the relative concentration of a secreted protein produced by transient transfection of mammalian cells in a bioreactor. Our results suggest that our approach can be readily applied to the at‐line determination of both protein concentration and bioactivity. Our experimental setup and strategy can thus satisfy the needs related to the development of novel bioprocess control protocols in the context of the new process analytical technology that arises in the biopharmaceutical industry. Biotechnol. Bioeng. 2008;100: 184–188. © 2007 Wiley Periodicals, Inc.
📜 SIMILAR VOLUMES
Two different strategies for scanning and screening of mutations in polymerase chain reaction (PCR) products by hybridization analysis are described, employing real-time biospecific interaction analysis (BIA) for detection. Real-time BIA was used to detect differences in hybridization responses betw
The performance of immunodiagnostic assays such as ELISA is governed by many different factors. Reflectometry was used to monitor peptide adsorption and the resulting antibody binding activity on a polystyrene surface. Surface plasmon resonance was used to analyze affinity and kinetic parameters of
Many sequences in genomic DNA are able to form unique tetraplex structures. Such structures are involved in a variety of important cellular processes and are emerging as a new class of therapeutic targets for cancers and other diseases. Screening for molecules targeting the tetraplex structure has b