发布: 2016年08月05日第6卷第15期 DOI: 10.21769/BioProtoc.1888 浏览次数: 10183
评审: Valentine V TrotterEsteban Paredes-OssesAnonymous reviewer(s)
相关实验方案
从大肠杆菌中大规模纯化III型毒素-抗毒素核糖蛋白复合物及其成分,用于生物物理学研究
Parthasarathy Manikandan [...] Mahavir Singh
2023年07月05日 834 阅读
Abstract
Heavy metals can cause damage to biomolecules such as proteins and DNA in multiple ways. Cells therefore strive for keeping intracellular (heavy) metal ions bound to specific proteins that are capable of handling detoxification, export or integration as cofactors. Metal binding proteins usually provide specific coordination sites that bind certain ions with ultrahigh affinity, with the thermodynamic driving force being the stability of organometallic complexes. However, the metal binding properties of these proteins can be highly variable. Therefore the transfer of specific ions between separate proteins or even between distinct binding sites located on one and the same protein does not always follow affinity gradients, but depends on particular protein interactions that are difficult to predict. We established a method suitable to probe metal transfer between two proteins, provided the proteins are amenable to purification and in vitro handling. It consists of the loading with metals, the co-incubation and the separation of metal-exchanging proteins with subsequent determination of bound metal content. The method is exemplified by experimental data of ours probing the transfer of copper(I) between the membrane-extrinsic metal binding domain MBD2 and the transmembrane domain of CopA, a copper export ATPase from Escherichia coli (Drees et al., 2015).
Keywords: Copper-binding protein (铜结合蛋白)Materials and Reagents
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文章信息
版权信息
© 2016 The Authors; exclusive licensee Bio-protocol LLC.
如何引用
Drees, S. L. and Lübben, M. (2016). Analytical Gel Filtration for Probing Heavy Metal Transfer between Proteins. Bio-protocol 6(15): e1888. DOI: 10.21769/BioProtoc.1888.
分类
生物化学 > 蛋白质 > 相互作用
微生物学 > 微生物生物化学 > 蛋白质
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