Mohammad Mohammad M, Movileanu Liviu
Department of Physics, Syracuse University, Syracuse, NY, USA.
Methods Mol Biol. 2012;870:21-37. doi: 10.1007/978-1-61779-773-6_2.
The use of nanopores is a powerful new frontier in single-molecule sciences. Nanopores have been used effectively in exploring various biophysical features of small polypeptides and proteins, such as their folding state and structure, ligand interactions, and enzymatic activity. In particular, the α-hemolysin (αHL) protein pore has been used extensively for the detection, characterization, and analysis of polypeptides because this protein nanopore is highly robust, versatile, and tractable under various experimental conditions. Inspired by the mechanisms of protein translocation across the outer membrane translocases of mitochondria, we have shown the ability to use nanopore-probe techniques in controlling a single protein using engineered αHL pores. Here, we provide a detailed protocol for the preparation of αHL protein nanopores. Moreover, we demonstrate that placing attractive electrostatic traps is instrumental in tackling single-molecule stochastic sensing of folded proteins.
纳米孔的应用是单分子科学领域一个强大的新前沿。纳米孔已被有效地用于探索小多肽和蛋白质的各种生物物理特性,如它们的折叠状态和结构、配体相互作用以及酶活性。特别是,α-溶血素(αHL)蛋白孔已被广泛用于多肽的检测、表征和分析,因为这种蛋白质纳米孔在各种实验条件下都具有高度的稳定性、通用性和易处理性。受蛋白质跨线粒体外膜转运酶转运机制的启发,我们已经展示了使用纳米孔探针技术通过工程化的αHL孔来控制单个蛋白质的能力。在这里,我们提供了一份详细的αHL蛋白纳米孔制备方案。此外,我们证明设置有吸引力的静电陷阱有助于解决折叠蛋白的单分子随机传感问题。