Meng Ran
Program in Computational Biology and Bioinformatics, Yale University, New Haven, CT, USA.
Department of Molecular Biophysics and Biochemistry, Yale University, New Haven, CT, USA.
Bio Protoc. 2024 Oct 20;14(20):e5094. doi: 10.21769/BioProtoc.5094.
Single-stranded RNA bacteriophages (ssRNA phages) infect their hosts by binding to the host receptor pili. Purification of pili usually involves mechanical shearing of pili from cells followed by precipitation. However, previous methods often result in low efficiency or unstable results due to pili retraction. This protocol presents an optimized method for purifying receptor type IV pili from (), incorporating enhancements in shearing and collection steps to achieve high yields. We found that repeated passage through syringe needles increases yield, and temperature control is crucial during purification. Additionally, the CsCl density gradient was optimized specifically for this specific strain. The purified type IV pili are suitable for cryogenic electron microscopy (cryo-EM) and various biochemical experiments. Key features • Pili purification for single-particle cryo-electron microscopy (Cryo-EM) analysis • This protocol builds upon the F-pili purification method developed by Costa et al. [1] extending its application to the 16. • It is optimized for higher and more stable pili yields, as well as increased reproducibility. • The method is tested on various bacterial species and can be adapted to purify different types of pili.
单链RNA噬菌体(ssRNA噬菌体)通过与宿主受体菌毛结合来感染宿主。菌毛的纯化通常包括从细胞中机械剪切菌毛,然后进行沉淀。然而,由于菌毛回缩,以前的方法往往效率低下或结果不稳定。本方案提出了一种从()中纯化IV型受体菌毛的优化方法,在剪切和收集步骤中进行了改进以实现高产率。我们发现,反复通过注射器针头可提高产量,并且在纯化过程中温度控制至关重要。此外,CsCl密度梯度针对该特定菌株进行了专门优化。纯化的IV型菌毛适用于低温电子显微镜(cryo-EM)和各种生化实验。关键特性 • 用于单颗粒低温电子显微镜(Cryo-EM)分析的菌毛纯化 • 本方案基于Costa等人[1]开发的F菌毛纯化方法,将其应用扩展到16。 • 针对更高且更稳定的菌毛产量以及更高的重现性进行了优化。 • 该方法已在多种细菌物种上进行测试,并且可适用于纯化不同类型的菌毛。