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A helix-to-coil transition at the ε-cut site in the transmembrane dimer of the amyloid precursor protein is required for proteolysis |
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| Authors: | Takeshi Sato Tzu-chun Tang Gabriella Reubins Jeffrey Z Fei Taiki Fujimoto Pascal Kienlen-Campard Stefan N Constantinescu Jean-Noel Octave Saburo Aimoto and Steven O Smith |
| Institution: | aDepartment of Biochemistry and Cell Biology, Center for Structural Biology, Stony Brook University, Stony Brook, NY 11794-5115; ;bInstitute for Protein Research, Osaka University, 3-2 Yamadaoka, Suita, Osaka 565-0871, Japan; ;cInstitute of Neuroscience, Université catholique de Louvain, Brussels 1200, Belgium; and ;dLudwig Institute for Cancer Research and de Duve Institute, Université catholique de Louvain, Brussels 1200, Belgium |
| Abstract: | Processing of amyloid precursor protein (APP) by γ-secretase is the last step in the formation of the Aβ peptides associated Alzheimer's disease. Solid-state NMR spectroscopy is used to establish the structural features of the transmembrane (TM) and juxtamembrane (JM) domains of APP that facilitate proteolysis. Using peptides corresponding to the APP TM and JM regions (residues 618–660), we show that the TM domain forms an α-helical homodimer mediated by consecutive GxxxG motifs. We find that the APP TM helix is disrupted at the intracellular membrane boundary near the ε-cleavage site. This helix-to-coil transition is required for γ-secretase processing; mutations that extend the TM α-helix inhibit ε cleavage, leading to a low production of Aβ peptides and an accumulation of the α- and β-C-terminal fragments. Our data support a progressive cleavage mechanism for APP proteolysis that depends on the helix-to-coil transition at the TM-JM boundary and unraveling of the TM α-helix. |
| Keywords: | Alzheimer''s disease GxxxG motifs progressive cleavage solid-state-NMR spectroscopy |