Hoarau Marie, Malbert Yannick, Irague Romain, Hureau Christelle, Faller Peter, Gras Emmanuel, André Isabelle, Remaud-Siméon Magali
Laboratoire d'Ingénierie des Systèmes Biologiques et Procédés, Université de Toulouse, CNRS, INRA, INSA, Toulouse, France.
Laboratoire de Chimie de Coordination, CNRS, Université de Toulouse, INPT, Toulouse, France.
PLoS One. 2016 Aug 17;11(8):e0161209. doi: 10.1371/journal.pone.0161209. eCollection 2016.
An improved production and purification method for Alzheimer's disease related methionine-modified amyloid-β 1-40 and 1-42 peptides is proposed, taking advantage of the formation of inclusion body in Escherichia coli. A Thioflavin-S assay was set-up to evaluate inclusion body formation during growth and optimize culture conditions for amyloid-β peptides production. A simple and fast purification protocol including first the isolation of the inclusion bodies and second, two cycles of high pH denaturation/ neutralization combined with an ultrafiltration step on 30-kDa cut-off membrane was established. Special attention was paid to purity monitoring based on a rational combination of UV spectrophotometry and SDS-PAGE analyses at the various stages of the process. It revealed that this chromatography-free protocol affords good yield of high quality peptides in term of purity. The resulting peptides were fully characterized and are appropriate models for highly reproducible in vitro aggregation studies.
提出了一种改进的生产和纯化与阿尔茨海默病相关的甲硫氨酸修饰淀粉样β蛋白1-40和1-42肽的方法,该方法利用了大肠杆菌中包涵体的形成。建立了硫黄素-S检测法,以评估生长过程中包涵体的形成,并优化淀粉样β肽生产的培养条件。建立了一种简单快速的纯化方案,首先分离包涵体,其次进行两个高pH变性/中和循环,并结合在30 kDa截留膜上的超滤步骤。在该过程的各个阶段,基于紫外分光光度法和SDS-PAGE分析的合理组合,特别关注纯度监测。结果表明,这种无色谱方法在纯度方面能提供高质量肽的良好产率。所得肽经过全面表征,是用于高度可重复的体外聚集研究的合适模型。