Peng Xiujuan, Leal Jasmim, Mohanty Rashmi, Soto Melissa, Ghosh Debadyuti
Division of Molecular Pharmaceutics and Drug Delivery, College of Pharmacy, University of Texas at Austin.
Division of Molecular Pharmaceutics and Drug Delivery, College of Pharmacy, University of Texas at Austin;
J Vis Exp. 2018 Sep 27(139):58165. doi: 10.3791/58165.
This protocol describes the use of quantitative PCR (qPCR) to enumerate T7 phages from phage selection experiments (i.e., "biopanning"). qPCR is a fluorescence-based approach to quantify DNA, and here, it is adapted to quantify phage genomes as a proxy for phage particles. In this protocol, a facile phage DNA preparation method is described using high-temperature heating without additional DNA purification. The method only needs small volumes of heat-treated phages and small volumes of the qPCR reaction. qPCR is high-throughput and fast, able to process and obtain data from a 96-well plate of reactions in 2-4 h. Compared to other phage enumeration approaches, qPCR is more time-efficient. Here, qPCR is used to enumerate T7 phages identified from biopanning against in vitro cystic fibrosis-like mucus model. The qPCR method can be extended to quantify T7 phages from other experiments, including other types of biopanning (e.g., immobilized protein binding, in vivo phage screening) and other sources (e.g., water systems or body fluids). In summary, this protocol can be modified to quantify any DNA-encapsulated viruses.
本方案描述了使用定量聚合酶链反应(qPCR)从噬菌体筛选实验(即“生物淘选”)中对T7噬菌体进行计数的方法。qPCR是一种基于荧光的DNA定量方法,在此,它被用于通过对噬菌体基因组进行定量来替代对噬菌体颗粒的定量。在本方案中,描述了一种简便的噬菌体DNA制备方法,该方法使用高温加热,无需额外的DNA纯化。该方法仅需要少量经热处理的噬菌体和少量的qPCR反应体系。qPCR具有高通量和快速的特点,能够在2-4小时内处理并从96孔板反应中获取数据。与其他噬菌体计数方法相比,qPCR更具时间效率。在此,qPCR用于对从针对体外囊性纤维化样黏液模型的生物淘选中鉴定出的T7噬菌体进行计数。qPCR方法可扩展用于对来自其他实验的T7噬菌体进行定量,包括其他类型的生物淘选(如固定化蛋白结合、体内噬菌体筛选)以及其他来源(如水系统或体液)。总之,本方案可经修改用于对任何DNA包裹的病毒进行定量。