Artificial, non-antibody binding proteins for pharmaceutical and industrial applications
- PMID: 16054718
- DOI: 10.1016/j.tibtech.2005.07.007
Artificial, non-antibody binding proteins for pharmaceutical and industrial applications
Abstract
Using combinatorial chemistry to generate novel binding molecules based on protein frameworks ('scaffolds') is a concept that has been strongly promoted during the past five years in both academia and industry. Non-antibody recognition proteins derive from different structural families and mimic the binding principle of immunoglobulins to varying degrees. In addition to the specific binding of a pre-defined target, these proteins provide favourable characteristics such as robustness, ease of modification and cost-efficient production. The broad spectrum of potential applications, including research tools, separomics, diagnostics and therapy, has led to the commercial exploitation of this technology by various small- and medium-sized companies. It is predicted that scaffold-based affinity reagents will broaden and complement applications that are presently covered by natural or recombinant antibodies. Here, we provide an overview on current approaches in the biotech industry, considering both scientific and commercial aspects.
Similar articles
-
Alternative non-antibody scaffolds for molecular recognition.Curr Opin Biotechnol. 2007 Aug;18(4):295-304. doi: 10.1016/j.copbio.2007.04.010. Epub 2007 Jul 20. Curr Opin Biotechnol. 2007. PMID: 17643280 Review.
-
A new generation of protein display scaffolds for molecular recognition.Protein Sci. 2006 Jan;15(1):14-27. doi: 10.1110/ps.051817606. Protein Sci. 2006. PMID: 16373474 Free PMC article. Review.
-
Binding proteins from alternative scaffolds.J Immunol Methods. 2004 Jul;290(1-2):3-28. doi: 10.1016/j.jim.2004.04.006. J Immunol Methods. 2004. PMID: 15261569 Review.
-
Alternative binding proteins: affibody binding proteins developed from a small three-helix bundle scaffold.FEBS J. 2008 Jun;275(11):2668-76. doi: 10.1111/j.1742-4658.2008.06438.x. Epub 2008 Apr 24. FEBS J. 2008. PMID: 18435759 Review.
-
[Development of antituberculous drugs: current status and future prospects].Kekkaku. 2006 Dec;81(12):753-74. Kekkaku. 2006. PMID: 17240921 Review. Japanese.
Cited by
-
Anti-Human VEGF Repebody Effectively Suppresses Choroidal Neovascularization and Vascular Leakage.PLoS One. 2016 Mar 25;11(3):e0152522. doi: 10.1371/journal.pone.0152522. eCollection 2016. PLoS One. 2016. PMID: 27015541 Free PMC article.
-
High-affinity target binding engineered via fusion of a single-domain antibody fragment with a ligand-tailored SH3 domain.PLoS One. 2012;7(7):e40331. doi: 10.1371/journal.pone.0040331. Epub 2012 Jul 5. PLoS One. 2012. PMID: 22792285 Free PMC article.
-
New binding mode to TNF-alpha revealed by ubiquitin-based artificial binding protein.PLoS One. 2012;7(2):e31298. doi: 10.1371/journal.pone.0031298. Epub 2012 Feb 20. PLoS One. 2012. PMID: 22363609 Free PMC article.
-
Peptide aptamers: development and applications.Curr Top Med Chem. 2015;15(12):1082-101. doi: 10.2174/1568026615666150413153143. Curr Top Med Chem. 2015. PMID: 25866267 Free PMC article. Review.
-
Engineering isoflavone metabolism with an artificial bifunctional enzyme.Planta. 2006 Aug;224(3):496-507. doi: 10.1007/s00425-006-0233-0. Epub 2006 Feb 16. Planta. 2006. PMID: 16482434
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Miscellaneous