amyloid-beta-peptides and triazacyclononane

amyloid-beta-peptides has been researched along with triazacyclononane* in 1 studies

Other Studies

1 other study(ies) available for amyloid-beta-peptides and triazacyclononane

Article	Year
Two nitrogen-containing ligands as inhibitors of metal-induced amyloid β-peptide aggregation. CNS & neurological disorders drug targets, 2014, Volume: 13, Issue:1 Abnormal interactions of Zn(2+) and Cu(2+) with the amyloid β-peptide (Aβ) are proposed to play an important role in the neuropathogenesis of Alzheimer's disease (AD). Metal chelators are potential therapeutic agents for AD because they could sequester metals ions from Aβ aggregates and reverse the aggregation. In this study, two nitrogencontaining ligands, TACN and BPA, have been investigated as possible metal chelators in the therapy of Alzheimer's disease. The interactions between the chelators and Aβ40 aggregates are studied by turbidometry, thioflavin T (ThT) fluorescence spectroscopy, inductively coupled plasma mass spectrometry (ICP-MS), BCA protein assay, circular dichroism spectroscopy (CD), and atomic force microscopy (AFM). The results demonstrates that TACN and BPA are capable of both disrupting and preventing Zn(2+) or Cu(2+)-induced Aβ40 aggregation. Moreover, they can also suppress the production of H2O2 induced by Cu-Aβ40, associated with toxic oxidative stress in AD. Topics: Amyloid beta-Peptides; Aza Compounds; Boron Compounds; Chelating Agents; Copper; Dose-Response Relationship, Drug; Humans; Metals; Microscopy, Atomic Force; Peptide Fragments; Phenylalanine; Piperidines; Protein Conformation; Spectrometry, Fluorescence; Zinc	2014

Article

Year

Two nitrogen-containing ligands as inhibitors of metal-induced amyloid β-peptide aggregation.

CNS & neurological disorders drug targets, 2014, Volume: 13, Issue:1

Abnormal interactions of Zn(2+) and Cu(2+) with the amyloid β-peptide (Aβ) are proposed to play an important role in the neuropathogenesis of Alzheimer's disease (AD). Metal chelators are potential therapeutic agents for AD because they could sequester metals ions from Aβ aggregates and reverse the aggregation. In this study, two nitrogencontaining ligands, TACN and BPA, have been investigated as possible metal chelators in the therapy of Alzheimer's disease. The interactions between the chelators and Aβ40 aggregates are studied by turbidometry, thioflavin T (ThT) fluorescence spectroscopy, inductively coupled plasma mass spectrometry (ICP-MS), BCA protein assay, circular dichroism spectroscopy (CD), and atomic force microscopy (AFM). The results demonstrates that TACN and BPA are capable of both disrupting and preventing Zn(2+) or Cu(2+)-induced Aβ40 aggregation. Moreover, they can also suppress the production of H2O2 induced by Cu-Aβ40, associated with toxic oxidative stress in AD.

Topics: Amyloid beta-Peptides; Aza Compounds; Boron Compounds; Chelating Agents; Copper; Dose-Response Relationship, Drug; Humans; Metals; Microscopy, Atomic Force; Peptide Fragments; Phenylalanine; Piperidines; Protein Conformation; Spectrometry, Fluorescence; Zinc

2014