Center for Eukaryotic Gene Regulation, Department of Biochemistry and Molecular Biology, The Pennsylvania State University, University Park, PA, 16802, USA.
Schreyer Honors College, The Pennsylvania State University, University Park, PA, 16802, USA.
Sci Rep. 2021 Aug 18;11(1):16703. doi: 10.1038/s41598-021-96051-x.
We have created the Penn State Protein Ladder system to produce protein molecular weight markers easily and inexpensively (less than a penny a lane). The system includes plasmids which express 10, 15, 20, 30, 40, 50, 60, 80 and 100 kD proteins in E. coli. Each protein migrates appropriately on SDS-PAGE gels, is expressed at very high levels (10-50 mg per liter of culture), is easy to purify via histidine tags and can be detected directly on Western blots via engineered immunoglobulin binding domains. We have also constructed plasmids to express 150 and 250 kD proteins. For more efficient production, we have created two polycistronic expression vectors which coexpress the 10, 30, 50, 100 kD proteins or the 20, 40, 60, 80 kD proteins. 50 ml of culture is sufficient to produce 20,000 lanes of individual ladder protein or 3750 lanes of each set of coexpressed ladder proteins. These Penn State Protein Ladder expression plasmids also constitute useful reagents for teaching laboratories to demonstrate recombinant expression in E. coli and affinity protein purification, and to research laboratories desiring positive controls for recombinant protein expression and purification.
我们创建了宾夕法尼亚州立蛋白梯系统,以便轻松且廉价地(每条泳道不到一美分)生产蛋白质分子量标记物。该系统包括在大肠杆菌中表达 10、15、20、30、40、50、60、80 和 100 kD 蛋白质的质粒。每种蛋白质在 SDS-PAGE 凝胶中迁移适当,表达水平非常高(每升培养物 10-50 毫克),易于通过组氨酸标签纯化,并可通过工程化免疫球蛋白结合结构域直接在 Western 印迹中检测到。我们还构建了表达 150 和 250 kD 蛋白质的质粒。为了提高生产效率,我们创建了两个多顺反子表达载体,可共表达 10、30、50、100 kD 蛋白质或 20、40、60、80 kD 蛋白质。50 毫升培养物足以产生 20000 条单独的梯状蛋白质泳道,或 3750 条共表达的梯状蛋白质泳道。这些宾夕法尼亚州立蛋白梯表达质粒也构成了教学实验室用于展示大肠杆菌中重组表达和亲和蛋白纯化的有用试剂,以及希望对重组蛋白表达和纯化进行阳性对照的研究实验室的有用试剂。