Klajnert B, Cladera J, Bryszewska M
Department of General Biophysics, University of Lodz, Poland.
Biomacromolecules. 2006 Jul;7(7):2186-91. doi: 10.1021/bm060229s.
The formation of amyloid plaques is a key pathological event in neurodegenerative disorders, such as prion and Alzheimer's diseases. Dendrimers are considered promising therapeutic agents in these disorders. In the present work, we have studied the effect of polypropyleneimine dendrimers on the formation of amyloid fibrils as a function of pH in order to gain further insight in the aggregation mechanism and its inhibition. Amyloid fibrils from prion peptide PrP 185-208 and Alzheimer's peptide Abeta 1-28 were produced in vitro, and their formation was monitored using the dye thioflavin T (ThT). The results showed that the level of protonation of His, Glu, and Asp residues is important for the final effect, especially at low dendrimer concentration when their inhibiting capacity depends on the pH. At the highest concentrations, dendrimers were very effective against fibril formations for both prion and Alzheimer's peptides.
淀粉样斑块的形成是神经退行性疾病(如朊病毒病和阿尔茨海默病)中的关键病理事件。树枝状聚合物被认为是治疗这些疾病的有前景的药物。在本研究中,我们研究了聚丙烯亚胺树枝状聚合物对淀粉样纤维形成的影响,并将其作为pH的函数,以便进一步深入了解聚集机制及其抑制作用。在体外产生了来自朊病毒肽PrP 185 - 208和阿尔茨海默病肽Abeta 1 - 28的淀粉样纤维,并用染料硫黄素T(ThT)监测它们的形成。结果表明,His、Glu和Asp残基的质子化水平对最终效果很重要,特别是在低树枝状聚合物浓度下,此时它们的抑制能力取决于pH。在最高浓度下,树枝状聚合物对朊病毒肽和阿尔茨海默病肽的纤维形成都非常有效。