Literature DB >> 8794167

Protein engineering and design for drug delivery.

J R Murphy1.   

Abstract

Over the past decade considerable effort has been focused on the genetic construction, expression, and characterization of fusion proteins designed to selectively target specific disease-causing cells and/or extracellular targets. In each instance, the coding sequences for the functional domains of different proteins have been genetically fused, resulting in the formation of fusion proteins which retain the function of their component segments. As anticipated from their design, many of these fusion proteins offer a marked therapeutic advantage over conventional agents in preclinical studies. While several recombinant fusion proteins have entered or will shortly begin Phase I/II human clinical trials, the first of these fusion proteins is currently being evaluated in Phase III human clinical trials for the treatment of cutaneous T cell lymphoma.

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Year:  1996        PMID: 8794167     DOI: 10.1016/s0959-440x(96)80121-7

Source DB:  PubMed          Journal:  Curr Opin Struct Biol        ISSN: 0959-440X            Impact factor:   6.809


  3 in total

1.  Contribution of proton linkage to the thermodynamic stability of the major cold-shock protein of Escherichia coli CspA.

Authors:  S A Petrosian; G I Makhatadze
Journal:  Protein Sci       Date:  2000-02       Impact factor: 6.725

2.  LINKER: a web server to generate peptide sequences with extended conformation.

Authors:  Fan Xue; Zhong Gu; Jin-an Feng
Journal:  Nucleic Acids Res       Date:  2004-07-01       Impact factor: 16.971

Review 3.  Mitochondrial medicine for neurodegenerative diseases.

Authors:  Heng Du; Shirley ShiDu Yan
Journal:  Int J Biochem Cell Biol       Date:  2010-01-11       Impact factor: 5.085

  3 in total

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