| Literature DB >> 31341020 |
Chiharu Mizuguchi1, Miho Nakagawa1, Norihiro Namba1, Misae Sakai1, Naoko Kurimitsu1, Ayane Suzuki1, Kaho Fujita1, Sayaka Horiuchi1, Teruhiko Baba2, Takashi Ohgita1, Kazuchika Nishitsuji3, Hiroyuki Saito4.
Abstract
The N-terminal (1-83) fragment of the major constituent of plasma high-density lipoprotein, apolipoprotein A-I (apoA-I), strongly tends to form amyloid fibrils, leading to systemic amyloidosis. Here, using a series of deletion variants, we examined the roles of two major amyloidogenic segments (residues 14-22 and 50-58) in the aggregation and fibril formation of an amyloidogenic G26R variant of the apoA-I 1-83 fragment (apoA-I 1-83/G26R). Thioflavin T fluorescence assays and atomic force microscopy revealed that elimination of residues 14-22 completely inhibits fibril formation of apoA-I 1-83/G26R, whereas Δ32-40 and Δ50-58 variants formed fibrils with markedly reduced nucleation and fibril growth rates. CD measurements revealed structural transitions from random coil to β-sheet structures in all deletion variants except for the Δ14-22 variant, indicating that residues 14-22 are critical for the β-transition and fibril formation. Thermodynamic analysis of the kinetics of fibril formation by apoA-I 1-83/G26R indicated that both nucleation and fibril growth are enthalpically unfavorable, whereas entropically, nucleation is favorable, but fibril growth is unfavorable. Interestingly, the nucleation of the Δ50-58 variant was entropically unfavorable, indicating that residues 50-58 entropically promote the nucleation step in fibril formation of apoA-I 1-83/G26R. Moreover, a residue-level structural investigation of apoA-I 1-83/G26R fibrils with site-specific pyrene labeling indicated that the two amyloidogenic segments are in close proximity to form an amyloid core structure, whereas the N- and C-terminal tail regions are excluded from the amyloid core. These results provide critical insights into the aggregation mechanism and fibril structure of the amyloidogenic N-terminal fragment of apoA-I.Entities:
Keywords: G26R variant; activation energy; amyloid; apolipoprotein; apolipoprotein A-I; fibril; hereditary systemic amyloidosis; protein aggregation; protein structure; pyrene labeling
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Year: 2019 PMID: 31341020 PMCID: PMC6737231 DOI: 10.1074/jbc.RA119.008000
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157