Journal article
Identification of an amyloid fibril forming peptide comprising residues 46-59 of apolipoprotein A-I
YQ Wong, KJ Binger, GJ Howlett, MDW Griffin
FEBS Letters | Published : 2012
Abstract
Apolipoprotein A-I (apoA-I) is deposited as amyloid within various major organs in hereditary apoA-I amyloidosis, and in arterial plaques associated with atherosclerosis. We have identified a tryptic fragment of apoA-I, apoA-I 46-59, that retains the ability to form amyloid-like fibrils with cross-β structure. ApoA-I 46-59 corresponds closely to a conformationally extended segment in the crystal structure of apoA-IΔ(185-243) and is located in the N-terminal region of apoA-I, which accumulates in hereditary apoA-I amyloidosis. Our results provide direct experimental evidence that this region of apoA-I is amyloidogenic and integral to initiation and propagation of amyloid formation by the prot..
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Awarded by Australian Research Council
Funding Acknowledgements
This research was supported by the Australian Research Council's Discovery Projects funding scheme (project number DP110103528). M. D. W. G. is the recipient of an Australian Research Council Post Doctoral Fellowship. Part of this research was undertaken at the MX1 beam-line of the Australian Synchrotron. The authors wish to thank John Karas for peptide synthesis.