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Article
Nature Medicine  3, 328 - 332 (1997)
doi:10.1038/nm0397-328

Formation of stable complexes between two Alzheimer's disease gene products: Presenilin-2 and bold beta-amyloid precursor protein

A. Weidemann1, K. Paliga1, U. Dürrwang1, C. Czech2, G. Evin3, C. L. Masters3 & K. Beyreuther1

  1Zentrum für Molekulare Biologie Heidelberg, ZMBH, INF 282, 69120 Heidelberg, Germany

  2Rhone-Poulenc Rarer, Vitry-sur-Seine, France

  3Department of Pathology, University of Melbourne, Parkvitte, Victoria 3052, Australia Correspondence should be addressed to A.W.

Mutations in the presenilin genes are associated with early onset familial Alzheimer's disease and lead to increased accumulation of betaA4 peptide, the proteolytic product of the amyloid precursor protein (APP). To test whether presenilins interfere with APP metabolism, presenilin-2 (PS2) was coexpressed with APP in mammalian cells. Analysis of PS2 immunoprecipitates revealed that a fraction of APP was associated with the PS2 immunocomplexes. This non-covalent association was specific for the APP family of proteins and restricted to immature forms, occuring probably during transit through the endoplasmic reticulum. Additionally, coexpression with PS2 resulted in a decrease of APP secretion, suggesting a direct participation of presenilins in the intracellular sorting, trafficking and processing of APP molecules.

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ISSN: 1078-8956
EISSN: 1546-170X
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