Calero Miguel, Rostagno Agueda, Ghiso Jorge
Centro Nacional de Microbiología, Instituto de Salud Carlos III, Majadahonda, Madrid, Spain.
Methods Mol Biol. 2012;849:213-23. doi: 10.1007/978-1-61779-551-0_15.
'Amyloid binging proteins' is a generic term used to designate proteins that interact with different forms of amyloidogenic peptides or proteins and that, as a result, may modulate their physiological and pathological functions by altering solubility, transport, clearance, degradation, and fibril formation. We describe a simple affinity chromatography protocol to isolate and characterize amyloid-binding proteins based on the use of sequential elution steps that may provide further information on the type of binding interaction. As an example, we depict the application of this protocol to the study of Alzheimer's amyloid β (Aβ) peptide-binding proteins derived from human plasma. Biochemical analysis of the proteins eluted under different conditions identified serum amyloid P component (SAP) and apolipoprotein J (clusterin) as the main plasma Aβ-binding proteins while various apolipoproteins (apoA-IV, apoE, and apoA-I), as well as albumin (HSA) and fibulin were identified as minor contributors.
“淀粉样蛋白结合蛋白”是一个通用术语,用于指代与不同形式的淀粉样生成肽或蛋白相互作用的蛋白,因此,它们可能通过改变溶解度、转运、清除、降解和纤维形成来调节其生理和病理功能。我们描述了一种简单的亲和色谱方法,用于基于连续洗脱步骤来分离和表征淀粉样蛋白结合蛋白,这些步骤可能会提供有关结合相互作用类型的更多信息。作为一个例子,我们描述了该方法在研究源自人血浆的阿尔茨海默病淀粉样β(Aβ)肽结合蛋白中的应用。对在不同条件下洗脱的蛋白质进行生化分析,确定血清淀粉样蛋白P成分(SAP)和载脂蛋白J(簇集蛋白)是主要的血浆Aβ结合蛋白,而各种载脂蛋白(载脂蛋白A-IV、载脂蛋白E和载脂蛋白A-I)以及白蛋白(HSA)和纤连蛋白是次要贡献者。