Literature DB >> 17028131

Time-dependent DNA condensation induced by amyloid beta-peptide.

Haijia Yu1, Jinsong Ren, Xiaogang Qu.   

Abstract

The major protein component of the amyloid deposition in Alzheimer's disease is a 39-43 residue peptide, amyloid beta (Abeta). Abeta is toxic to neurons, although the mechanism of neurodegeneration is uncertain. Evidence exists for non-B DNA conformation in the hippocampus of Alzheimer's disease brains, and Abeta was reportedly able to transform DNA conformation in vitro. In this study, we found that DNA conformation was altered in the presence of Abeta, and Abeta induced DNA condensation in a time-dependent manner. Furthermore, Abeta sheets, serving as condensation nuclei, were crucial for DNA condensation, and Cu(2+) and Zn(2+) ions inhibited Abeta sheet-induced DNA condensation. Our results suggest DNA condensation as a mechanism of Abeta toxicity.

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Year:  2006        PMID: 17028131      PMCID: PMC1697842          DOI: 10.1529/biophysj.106.093559

Source DB:  PubMed          Journal:  Biophys J        ISSN: 0006-3495            Impact factor:   4.033


  45 in total

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2.  Cu(2+) Inhibits the Aggregation of Amyloid beta-Peptide(1-42) in vitro We thank JEOL for the AFM measurement. This work was supported in part by Grants-in-Aid from the Japanese Ministry of Education, Science, Sports, and Culture, and a Grant from "Research for the Future" Program of the Japan Society for the Promotion of Science to N.S.

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6.  Secondary structural complementarity between DNA and proteins.

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4.  Binding with nucleic acids or glycosaminoglycans converts soluble protein oligomers to amyloid.

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Review 8.  Functional Reciprocity of Amyloids and Antimicrobial Peptides: Rethinking the Role of Supramolecular Assembly in Host Defense, Immune Activation, and Inflammation.

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9.  Ascovirus P64 Homologs: A Novel Family of Large Cationic Proteins That Condense Viral Genomic DNA for Encapsidation.

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10.  Prion Protein PRNP: A New Player in Innate Immunity? The Aβ Connection.

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