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Amyloid beta-protein (A beta) associated with lipid molecules: immunoreactivity distinct from that of soluble A beta.
Yanagisawa, K; McLaurin, J; Michikawa, M; Chakrabartty, A; Ihara, Y.
Affiliation
  • Yanagisawa K; Department of Dementia Research, National Institute for Longevity Sciences, Morioka, Obu, Japan. katuhiko@nils.go.jp
FEBS Lett ; 420(1): 43-6, 1997 Dec 22.
Article in En | MEDLINE | ID: mdl-9450547
ABSTRACT
We previously identified a novel amyloid beta-protein (A beta), that binds to GM1 ganglioside, in brains exhibiting the early pathological changes of AD. In this study, we raised monoclonal antibodies, using membrane fractions containing abundant GM1 ganglioside-bound A beta as antigens. Monoclonal antibody 4396, produced in this study, immunoprecipitates A beta42 in the membrane fractions of brains with diffuse plaques, but does not react with soluble A beta42 or GM1 ganglioside. Furthermore, this antibody recognizes the A beta bound to lipid vesicles containing GM1 ganglioside, and unexpectedly, phosphatidylinositol. In contrast, a control anti-A beta monoclonal antibody does not recognize the A beta bound to these lipid vesicles. These results indicate that A beta associated with lipids has an immunoreactivity distinct from that of soluble A.
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Collection: 01-internacional Database: MEDLINE Main subject: Amyloid beta-Peptides / Lipid Metabolism / G(M1) Ganglioside Type of study: Risk_factors_studies Limits: Animals / Female / Humans Language: En Journal: FEBS Lett Year: 1997 Type: Article Affiliation country: Japan
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Collection: 01-internacional Database: MEDLINE Main subject: Amyloid beta-Peptides / Lipid Metabolism / G(M1) Ganglioside Type of study: Risk_factors_studies Limits: Animals / Female / Humans Language: En Journal: FEBS Lett Year: 1997 Type: Article Affiliation country: Japan