Elsevier

Neuroscience Letters

Volume 349, Issue 2, 2 October 2003, Pages 133-135
Neuroscience Letters

Epitope mapping and specificity of the anti-α-synuclein monoclonal antibody Syn-1 in mouse brain and cultured cell lines

https://doi.org/10.1016/S0304-3940(03)00781-XGet rights and content

Abstract

While α- and β-synuclein largely overlap in their expression in the vertebrate brain, only α-synuclein accumulates in the fibrillar aggregates typical of Parkinson's disease. It is thus critical to have immunological reagents that distinguish between these two protein isoforms. The monoclonal antibody Syn-1 (Transduction Labs) has been frequently used for the specific detection of α-synuclein. In this report, the epitope for Syn-1 is localized within residues 91–99 of human α-synuclein. Sequence differences exist in this domain that account for the specificity of Syn-1 for α- versus β-synuclein. However, Syn-1 also displays reactivity with additional species (∼45 kDa) in brain homogenates from both wild-type and α-synuclein null mice, indicating a potential for cross-reactivity with a protein species that is unrelated to α-synuclein in brain tissue or extracts.

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Acknowledgements

This material is based upon work supported by the National Institute on Aging under Award #NIH R01 AG13762. Any opinions, findings, and conclusions or recommendations expressed in this publication are those of the authors and do not necessarily reflect the views of the NIA. R.P. received support from the Parkinson's Disease Foundation and the American Parkinson Disease Association. The authors wish to thank Dr William Dauer for the generous gift of his α-synuclein null mouse, Dr Benoit Giasson

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