Challenges in Integrative Research in
Therapeutic and Diagnostic Proteins:
Translation and Conformational Engineering
Volume 2 - Issue 3
Ajay K Ray*
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- Department of Chemical and Biochemical Engineering, University of Western Ontario, Canada
*Corresponding author:
Ajay K Ray, Department of Chemical and Biochemical Engineering, University of Western Ontario, Canada
Received: April 06, 2018; Published: April 16, 2018
DOI: 10.32474/OAJBEB.2018.02.000138
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Abstract
Biopharmaceuticals are mostly protein-derived medical
drugs play vital roles in the human body catalyzing sequence of
biochemical reactions. These biologics, which include therapeutic
proteins, monoclonal antibodies (MAbs), vaccines, hormones, and
fusion proteins, are used in the treatment, diagnosis and prevention
of specific diseases such as cancer, multiple sclerosis, rheumatoid
arthritis, diabetes, and a variety of cardiovascular diseases [1-3].
They are large molecular weight compounds with complex 3D
structures mimicking molecules found in human bodies. Their
production by living cells makes them different from classical small
molecular weight chemical drugs (e.g., antibiotics) and in general,
protein drug production by living cells is generally difficult [3]. With
the advent of recombinant DNA technology, the post genomic era is
seeing a massive increase in valuable protein products entering the
clinical trials to manage disease with high specificity [4]. The global
market for recombinant bio-pharmaceuticals has been growing
rapidly from 30 products with a market value of USD $50-60 billion
in 2004 to more than 151 unique products approved by the FDA by
2012 valued at USD $138 billion and is expected to surpass $320
billion by 2020.
Abbrevations: MAbs: Monoclonal Antibodies; CHO: Chinese Hamster Ovary; MCCSMB: Multiple Column Chromatography Based
on Simulated Moving Bed Technology
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