Literature DB >> 16054718

Artificial, non-antibody binding proteins for pharmaceutical and industrial applications.

Thomas Hey1, Erik Fiedler, Rainer Rudolph, Markus Fiedler.   

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.

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Year:  2005        PMID: 16054718     DOI: 10.1016/j.tibtech.2005.07.007

Source DB:  PubMed          Journal:  Trends Biotechnol        ISSN: 0167-7799            Impact factor:   19.536


  31 in total

Review 1.  Engineered CH2 domains (nanoantibodies).

Authors:  Dimiter S Dimitrov
Journal:  MAbs       Date:  2009 Jan-Feb       Impact factor: 5.857

2.  A large human domain antibody library combining heavy and light chain CDR3 diversity.

Authors:  Weizao Chen; Zhongyu Zhu; Yang Feng; Dimiter S Dimitrov
Journal:  Mol Immunol       Date:  2009-11-01       Impact factor: 4.407

Review 3.  Pharmacokinetics, pharmacodynamics and physiologically-based pharmacokinetic modelling of monoclonal antibodies.

Authors:  Miroslav Dostalek; Iain Gardner; Brian M Gurbaxani; Rachel H Rose; Manoranjenni Chetty
Journal:  Clin Pharmacokinet       Date:  2013-02       Impact factor: 6.447

4.  Expression, purification, and characterization of engineered antibody CH2 and VH domains.

Authors:  Rui Gong; Weizao Chen; Dimiter S Dimitrov
Journal:  Methods Mol Biol       Date:  2012

5.  Chimeric Antigen Receptors Incorporating D Domains Targeting CD123 Direct Potent Mono- and Bi-specific Antitumor Activity of T Cells.

Authors:  Haiying Qin; Justin P Edwards; Liubov Zaritskaya; Ankit Gupta; C Jenny Mu; Terry J Fry; David M Hilbert; David W LaFleur
Journal:  Mol Ther       Date:  2019-04-17       Impact factor: 11.454

6.  Derivative of Extremophilic 50S Ribosomal Protein L35Ae as an Alternative Protein Scaffold.

Authors:  Anna V Lomonosova; Andrei B Ulitin; Alexei S Kazakov; Tajib A Mirzabekov; Eugene A Permyakov; Sergei E Permyakov
Journal:  PLoS One       Date:  2017-01-19       Impact factor: 3.240

7.  Alanine substitutions of noncysteine residues in the cysteine-stabilized alphabeta motif.

Authors:  Ying-Fang Yang; Kuo-Chang Cheng; Ping-Hsing Tsai; Chung-Cheng Liu; Tian-Ren Lee; Ping-Chiang Lyu
Journal:  Protein Sci       Date:  2009-07       Impact factor: 6.725

8.  CD19 CAR T Cells for the Treatment of Pediatric Pre-B Cell Acute Lymphoblastic Leukemia.

Authors:  Holly L Pacenta; Theodore W Laetsch; Samuel John
Journal:  Paediatr Drugs       Date:  2020-02       Impact factor: 3.022

9.  Engineering isoflavone metabolism with an artificial bifunctional enzyme.

Authors:  L Tian; R A Dixon
Journal:  Planta       Date:  2006-02-16       Impact factor: 4.116

10.  Interrogating and predicting tolerated sequence diversity in protein folds: application to E. elaterium trypsin inhibitor-II cystine-knot miniprotein.

Authors:  Jennifer L Lahti; Adam P Silverman; Jennifer R Cochran
Journal:  PLoS Comput Biol       Date:  2009-09-04       Impact factor: 4.475

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