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Rational Design of Biobetters with Enhanced Stability.
- Source :
-
Journal of pharmaceutical sciences [J Pharm Sci] 2015 Aug; Vol. 104 (8), pp. 2433-40. Date of Electronic Publication: 2015 Jun 10. - Publication Year :
- 2015
-
Abstract
- Biotherapeutics are the fastest growing class of pharmaceutical with a rapidly evolving market facing the rise of biosimilar and biobetter products. In contrast to a biosimilar, which is derived from the same gene sequence as the innovator product, a biobetter has enhanced properties, such as enhanced efficacy or reduced immunogenicity. Little work has been carried out so far to increase the intrinsic stability of biotherapeutics via sequence changes, even though, aggregation, the primary degradation pathway of proteins, leads to issues ranging from manufacturing failure to immunological response and to loss of therapeutic activity. Using our spatial aggregation propensity tool as a first step to a rational design approach to identify aggregation-prone regions, biobetters of rituximab have been produced with enhanced stability by introducing site-specific mutations. Significant stabilization against aggregation was achieved for rituximab with no decrease in its binding affinity to the antigen.<br /> (© 2015 Wiley Periodicals, Inc. and the American Pharmacists Association.)
- Subjects :
- Amino Acid Substitution
Animals
Antibodies, Monoclonal, Humanized adverse effects
Antibodies, Monoclonal, Humanized chemistry
Antibodies, Monoclonal, Humanized metabolism
Antibodies, Monoclonal, Humanized pharmacology
Antibody Affinity
Antigens, CD20 chemistry
Antineoplastic Agents adverse effects
Antineoplastic Agents metabolism
Antineoplastic Agents pharmacology
B-Lymphocytes drug effects
B-Lymphocytes metabolism
Burkitt Lymphoma drug therapy
Burkitt Lymphoma metabolism
Cell Line, Tumor
Drug Stability
Epitopes metabolism
Humans
Immunoglobulin Fab Fragments chemistry
Immunoglobulin Fab Fragments genetics
Immunoglobulin Fab Fragments metabolism
Immunoglobulin Fab Fragments pharmacology
Mutagenesis, Site-Directed
Mutant Proteins adverse effects
Mutant Proteins metabolism
Mutant Proteins pharmacology
Protein Aggregates
Protein Stability
Recombinant Proteins adverse effects
Recombinant Proteins chemistry
Recombinant Proteins metabolism
Recombinant Proteins pharmacology
Rituximab genetics
Rituximab metabolism
Rituximab pharmacology
Antigens, CD20 metabolism
Antineoplastic Agents chemistry
Drug Design
Models, Molecular
Mutant Proteins chemistry
Protein Engineering
Rituximab chemistry
Subjects
Details
- Language :
- English
- ISSN :
- 1520-6017
- Volume :
- 104
- Issue :
- 8
- Database :
- MEDLINE
- Journal :
- Journal of pharmaceutical sciences
- Publication Type :
- Academic Journal
- Accession number :
- 26096711
- Full Text :
- https://doi.org/10.1002/jps.24520