Racemization: its biological significance on neuropathogenesis of Alzheimer's disease - PubMed (original) (raw)
Comparative Study
. 1994 Nov;174(3):251-62.
doi: 10.1620/tjem.174.251.
Affiliations
- PMID: 7761990
- DOI: 10.1620/tjem.174.251
Free article
Comparative Study
Racemization: its biological significance on neuropathogenesis of Alzheimer's disease
H Mori et al. Tohoku J Exp Med. 1994 Nov.
Free article
Abstract
Amyloid beta protein (A beta) in neuritic plaques of Alzheimer's disease has been found to be racemized and/or isomerized at their Asp residues. To elucidate the effect of racemization on the aggregation properties of A beta, we synthesized three kinds of A beta peptides in which D-Asp was substituted for L-Asp residues, i.e, normal A beta 1-40, [D-Asp7]A beta 1-40 and [D-Asp23]A beta 1-40. The aggregation and fibril formation of each peptide was examined by means of spectrofluorometry and electron microscopy. Of the three peptides, normal A beta showed the gradual increase of aggregation while [D-Asp7]A beta 1-40 and [D-Asp23] A beta 1-40 showed more enhanced aggregation at the final stage when the fibril formations were detected in all peptides solutions by electron microscopy. A comparative immunohistochemical study by anti-racemized A beta antibody and anti-A beta 1-42/43 antibody further showed the in vivo incorporation of D-Asp in senile plaques of Alzheimer's disease brains, which may be involved in plaque formation at the later stage than the deposition of the longer form of A beta (A beta 1-42/43). Taken together with the recent accumulated evidence on the aggregation mechanisms of A beta, the data presented here suggest that racemization may occur after the amyloid fibril formation but enhance the aggregation process by shifting the equilibrium of A beta from the soluble form to the insoluble form in Alzheimer's disease.
Similar articles
- Racemization of Asp23 residue affects the aggregation properties of Alzheimer amyloid beta protein analogues.
Tomiyama T, Asano S, Furiya Y, Shirasawa T, Endo N, Mori H. Tomiyama T, et al. J Biol Chem. 1994 Apr 8;269(14):10205-8. J Biol Chem. 1994. PMID: 8144598 - Site-specific aspartic acid isomerization regulates self-assembly and neurotoxicity of amyloid-β.
Sugiki T, Utsunomiya-Tate N. Sugiki T, et al. Biochem Biophys Res Commun. 2013 Nov 15;441(2):493-8. Biochem Biophys Res Commun. 2013. PMID: 24383085 - Isoaspartate formation and neurodegeneration in Alzheimer's disease.
Shimizu T, Watanabe A, Ogawara M, Mori H, Shirasawa T. Shimizu T, et al. Arch Biochem Biophys. 2000 Sep 15;381(2):225-34. doi: 10.1006/abbi.2000.1955. Arch Biochem Biophys. 2000. PMID: 11032409 Review. - Physicochemical characteristics of soluble oligomeric Abeta and their pathologic role in Alzheimer's disease.
Watson D, Castaño E, Kokjohn TA, Kuo YM, Lyubchenko Y, Pinsky D, Connolly ES Jr, Esh C, Luehrs DC, Stine WB, Rowse LM, Emmerling MR, Roher AE. Watson D, et al. Neurol Res. 2005 Dec;27(8):869-81. doi: 10.1179/016164105X49436. Neurol Res. 2005. PMID: 16354549 Review.
Cited by
- Fundamental Clock of Biological Aging: Convergence of Molecular, Neurodegenerative, Cognitive and Psychiatric Pathways: Non-Equilibrium Thermodynamics Meet Psychology.
Dyakin VV, Dyakina-Fagnano NV, Mcintire LB, Uversky VN. Dyakin VV, et al. Int J Mol Sci. 2021 Dec 28;23(1):285. doi: 10.3390/ijms23010285. Int J Mol Sci. 2021. PMID: 35008708 Free PMC article. Review. - Racemization in Post-Translational Modifications Relevance to Protein Aging, Aggregation and Neurodegeneration: Tip of the Iceberg.
Dyakin VV, Wisniewski TM, Lajtha A. Dyakin VV, et al. Symmetry (Basel). 2021 Mar;13(3):455. doi: 10.3390/sym13030455. Epub 2021 Mar 11. Symmetry (Basel). 2021. PMID: 34350031 Free PMC article. - Chiral Interface of Amyloid Beta (Aβ): Relevance to Protein Aging, Aggregation and Neurodegeneration.
Dyakin VV, Wisniewski TM, Lajtha A. Dyakin VV, et al. Symmetry (Basel). 2020 Apr;12(4):585. doi: 10.3390/sym12040585. Epub 2020 Apr 7. Symmetry (Basel). 2020. PMID: 34327009 Free PMC article. - Transient dynamics of Aβ contribute to toxicity in Alzheimer's disease.
Hubin E, van Nuland NA, Broersen K, Pauwels K. Hubin E, et al. Cell Mol Life Sci. 2014 Sep;71(18):3507-21. doi: 10.1007/s00018-014-1634-z. Epub 2014 May 7. Cell Mol Life Sci. 2014. PMID: 24803005 Free PMC article. Review. - N-truncated amyloid β (Aβ) 4-42 forms stable aggregates and induces acute and long-lasting behavioral deficits.
Bouter Y, Dietrich K, Wittnam JL, Rezaei-Ghaleh N, Pillot T, Papot-Couturier S, Lefebvre T, Sprenger F, Wirths O, Zweckstetter M, Bayer TA. Bouter Y, et al. Acta Neuropathol. 2013 Aug;126(2):189-205. doi: 10.1007/s00401-013-1129-2. Epub 2013 May 18. Acta Neuropathol. 2013. PMID: 23685882 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical