Hill Elisabeth K, Krebs Benjamin, Goodall Dianna G, Howlett Geoffrey J, Dunstan Dave E
Department of Chemical & Biomolecular Engineering and Department of Biochemistry & Molecular Biology, University of Melbourne, Victoria 3010, Australia.
Biomacromolecules. 2006 Jan;7(1):10-3. doi: 10.1021/bm0505078.
Shear flow is indirectly implicated in amyloid formation in vitro. Despite the association between amyloid fibrils and disease, and the prevalence of flow in physiological systems, the effect of this parameter is uncharacterized. We designed a novel Couette cell to quantitatively investigate shear exposure during fibrillogenesis. Amyloid formation by beta-lactoglobulin was monitored in situ with real-time fluorescence measurements across a range of shear rates. We demonstrate shear-induced aggregation of spheroidal seed-like species. These seeds enhance fibril formation in native beta-lactoglobulin, thereby demonstrating that shear flow generates an amyloidogenic precursor. Furthermore, preformed fibrils are degraded by exposure to high shear rates. Our results have implications for the mechanism of amyloid formation in physiological flow conditions.
在体外,剪切流与淀粉样蛋白的形成存在间接关联。尽管淀粉样纤维与疾病之间存在关联,且生理系统中普遍存在流动现象,但该参数的影响尚未得到明确表征。我们设计了一种新型库埃特流动腔,以定量研究原纤维形成过程中的剪切暴露情况。通过实时荧光测量,在一系列剪切速率下原位监测β-乳球蛋白的淀粉样蛋白形成过程。我们证明了剪切诱导的球状种子样物质的聚集。这些种子增强了天然β-乳球蛋白中原纤维的形成,从而表明剪切流产生了一种淀粉样蛋白生成前体。此外,预先形成的原纤维会因暴露于高剪切速率而降解。我们的研究结果对生理流动条件下淀粉样蛋白形成的机制具有启示意义。