Piazza Roberto, Pierno Matteo, Iacopini Sara, Mangione Palma, Esposito Gennaro, Bellotti Vittorio
Dipartimento di Ingegneria Nucleare, Politecnico di Milano, via Ponzio 34/3, 20133, Milano, Italy.
Eur Biophys J. 2006 May;35(5):439-45. doi: 10.1007/s00249-006-0051-0. Epub 2006 Mar 7.
We show that beta(2)-microglobulin solutions in physiological conditions contain a tiny fraction of aggregates, which can hardly be filtered out and tend to re-form spontaneously. At physiological pH the fractional amount and size distribution of the latter aggregates do not depend on temperature. Conversely, in the pH range typical of the peri-articular tissue acidosis that often occurs in hemodialysis, temperature increase leads to fast and irreversible growth of the aggregates. Quite similar, but strongly enhanced aggregation effects can be induced even in physiological conditions by adding a very small amount of DeltaN6, a naturally occurring truncated isoform of beta(2)-m known to promote fibrillogenesis.
我们发现,在生理条件下,β2-微球蛋白溶液中含有一小部分聚集体,这些聚集体几乎无法被过滤掉,并且倾向于自发重新形成。在生理pH值下,后一种聚集体的分数含量和尺寸分布不依赖于温度。相反,在血液透析中经常出现的关节周围组织酸中毒的典型pH范围内,温度升高会导致聚集体快速且不可逆地生长。即使在生理条件下,通过添加极少量的DeltaN6(一种已知可促进纤维形成的β2-微球蛋白天然截短异构体),也可以诱导出非常相似但强烈增强的聚集效应。