4.7 Review

Longer action means better drug: Tuning up protein therapeutics

期刊

BIOTECHNOLOGY ADVANCES
卷 29, 期 4, 页码 436-441

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.biotechadv.2011.03.005

关键词

Protein drugs; Protein stability; In vivo half-life; Protein engineering

资金

  1. Ministry of Science and Higher Education, Poland [NN302 2522 33]
  2. Norway through the Norwegian Financial Mechanism [PNRF-87-AI-1/07]

向作者/读者索取更多资源

An increasing number of proteins are currently available on the market as therapeutics and this branch of the pharmaceutical industry will expand substantially during the coming years. As many diseases result from dysfunction of proteins forming multicomponent complexes, protein drugs with their inherent high specificity and affinity seem to be optimal medical agents. On the other hand, proteins are often highly instable and sensitive to degradation, which questions their applicability as effective therapeutics. Therefore, redesign and engineering of proteins is usually a required step in the present day drug development. Several approaches have been applied to optimize the protein properties central to their pharmaceutical use. This review focuses on different strategies that improve two crucial factors influencing protein drug efficiency: protein stability and its in vivo half-life. We provide examples of successful genetic and chemical modifications applied in the design of effective protein therapeutics. (C) 2011 Elsevier Inc. All rights reserved.

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