Dey Supratim, Gireesan Saurabh, Solovou Theodora, Inniss Nicole L, Satchell Karla J F
Department of Microbiology-Immunology and Center for Structural Biology of Infectious Diseases, Feinberg School of Medicine, Northwestern University, Chicago, Illinois.
Curr Protoc. 2025 Jul;5(7):e70188. doi: 10.1002/cpz1.70188.
High-throughput protein expression and purification can now take advantage of the copious expansion of genes from extensive genomics and metagenomic surveillance programs. This article outlines a pipeline that involves strategic selection of a large repertoire of protein targets for cloning by commercial synthetic services, followed by high-throughput transformation, expression, and solubility screening. This pipeline will be applicable to structural and functional genomics approaches, as well as any project that requires large-scale screening for production of soluble proteins in a time-efficient manner. The protocols involve transformation, protein expression and solubility determination in a high-throughput fashion in a 96-well plate format. Proteins screened in this pipeline are then able to be purified for any assay needed. © 2025 The Author(s). Current Protocols published by Wiley Periodicals LLC. Basic Protocol 1: Target optimization Basic Protocol 2: High-throughput transformation Basic Protocol 3: High-throughput expression and solubility screening.
高通量蛋白质表达和纯化现在可以利用广泛的基因组学和宏基因组监测计划中大量扩增的基因。本文概述了一种流程,该流程包括通过商业合成服务从大量蛋白质靶标中进行战略选择以进行克隆,然后进行高通量转化、表达和溶解性筛选。该流程将适用于结构和功能基因组学方法,以及任何需要以高效方式大规模筛选可溶性蛋白质生产的项目。这些方案涉及以96孔板形式进行高通量转化、蛋白质表达和溶解性测定。在此流程中筛选出的蛋白质随后能够被纯化以用于任何所需的分析。© 2025作者。由Wiley Periodicals LLC出版的《当前方案》。基本方案1:靶标优化 基本方案2:高通量转化 基本方案3:高通量表达和溶解性筛选