Literature DB >> 17176119

The therapeutic potential of intrabodies in neurologic disorders: focus on Huntington and Parkinson diseases.

Anne Messer1, Julie McLear.   

Abstract

Single-chain Fv and single-domain antibodies retain the binding specificity of full-length antibodies but they can be cloned, selected, engineered, and manipulated as genes. When expressed intracellularly in mammalian cells these intracellular antibodies, or intrabodies, have the potential to alter the folding, interactions, modifications, or subcellular localization of their targets. These reagents have previously been developed as therapeutics against cancer and HIV. Since misfolded and accumulated intracellular proteins characterize several major neurodegenerative disorders, including Huntington disease (HD) and Parkinson disease, these disorders are prime candidates for intrabody therapy. In this article we review the extension of intrabody technology to the nervous system. Studies of HD have been used to develop the approach and anti-synuclein strategies are in the early stages of development. Such neurodegenerative diseases are therefore poised for engineered antibody approaches, which can provide a pipeline of novel therapeutics and new drug discovery tools.

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Year:  2006        PMID: 17176119     DOI: 10.2165/00063030-200620060-00002

Source DB:  PubMed          Journal:  BioDrugs        ISSN: 1173-8804            Impact factor:   5.807


  11 in total

Review 1.  Engineered antibody therapies to counteract mutant huntingtin and related toxic intracellular proteins.

Authors:  David C Butler; Julie A McLear; Anne Messer
Journal:  Prog Neurobiol       Date:  2011-11-18       Impact factor: 11.685

2.  Assessment of the efficacy of solutes from extremophiles on protein aggregation in cell models of Huntington's and Parkinson's diseases.

Authors:  Carla D Jorge; Rita Ventura; Christopher Maycock; Tiago F Outeiro; Helena Santos; Júlia Costa
Journal:  Neurochem Res       Date:  2011-03-17       Impact factor: 3.996

3.  Early or late-stage anti-N-terminal Huntingtin intrabody gene therapy reduces pathological features in B6.HDR6/1 mice.

Authors:  Abigail Snyder-Keller; Julie A McLear; Tyisha Hathorn; Anne Messer
Journal:  J Neuropathol Exp Neurol       Date:  2010-10       Impact factor: 3.685

4.  Engineering antibody fragments to fold in the absence of disulfide bonds.

Authors:  Min Jeong Seo; Ki Jun Jeong; Clinton E Leysath; Andrew D Ellington; Brent L Iverson; George Georgiou
Journal:  Protein Sci       Date:  2009-02       Impact factor: 6.725

5.  Intrabodies binding the proline-rich domains of mutant huntingtin increase its turnover and reduce neurotoxicity.

Authors:  Amber L Southwell; Ali Khoshnan; Denise E Dunn; Charles W Bugg; Donald C Lo; Paul H Patterson
Journal:  J Neurosci       Date:  2008-09-03       Impact factor: 6.167

6.  An scFv intrabody against the nonamyloid component of alpha-synuclein reduces intracellular aggregation and toxicity.

Authors:  Sandra M Lynch; Chun Zhou; Anne Messer
Journal:  J Mol Biol       Date:  2007-12-05       Impact factor: 5.469

Review 7.  alpha-Synuclein: a therapeutic target for Parkinson's disease?

Authors:  Kathleen A Maguire-Zeiss
Journal:  Pharmacol Res       Date:  2008-09-16       Impact factor: 7.658

8.  Functional protein delivery into neurons using polymeric nanoparticles.

Authors:  Linda Hasadsri; Jörg Kreuter; Hiroaki Hattori; Tadao Iwasaki; Julia M George
Journal:  J Biol Chem       Date:  2009-01-07       Impact factor: 5.157

Review 9.  Intrabodies as neuroprotective therapeutics.

Authors:  Anne Messer; Shubhada N Joshi
Journal:  Neurotherapeutics       Date:  2013-07       Impact factor: 7.620

10.  Bifunctional anti-huntingtin proteasome-directed intrabodies mediate efficient degradation of mutant huntingtin exon 1 protein fragments.

Authors:  David C Butler; Anne Messer
Journal:  PLoS One       Date:  2011-12-22       Impact factor: 3.240

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