The Impact of the 'Austrian' Mutation of the Amyloid Precursor Protein Transmembrane Helix is Communicated to the Hinge Region. Issue 15 (16th September 2016)

• Record Type: Journal Article
• Authors: Stelzer, Walter; Scharnagl, Christina; Leurs, Ulrike; Rand, Kasper D.; Langosch, Dieter
• Is Part Of: ChemistrySelect. Volume 1:Issue 15(2016)
• Page Start: 4408
• Page End: 4412
• Publication Date: 2016-09-16
• Subjects: Alzheimer's disease -- Amyloid beta-peptides -- deuterium/hydrogen exchange -- mass spectrometry -- transmembrane helix; Chemistry -- Periodicals; 540.5
• DOI: 10.1002/slct.201601090
• Languages: English
• ISSNs: 2365-6549

Abstract

Abstract: The transmembrane helix of the amyloid precursor protein is subject to proteolytic cleavages by γ‐secretase at different sites resulting in Aβ peptides of different length and toxicity. A number of point mutations within this transmembrane helix alter the cleavage pattern thus enhancing production of toxic Aβ peptide species that are at the root of familial Alzheimer's disease. Here, we investigated how one of the most devastating mutations, the 'Austrian' mutation T43I, affects this transmembrane helix. Site‐resolved deuterium/hydrogen amide exchange experiments reveal that the mutation destabilizes amide hydrogen bonds in the hinge which connects dimerization and cleavage regions. Weaker intrahelical hydrogen bonds at the hinge may enhance helix bending and thereby affect recognition of the transmembrane substrate by the enzyme and/or presentation of its cleavage sites to the catalytic cleft. Abstract : The 'Austrian' mutation T43I within the transmembrane helix of the amyloid precursor protein influences its hinge region. We suggest a mechanism by which T43I may accelerate the development of Alzheimer's disease in affected patients.