The Penn State Protein Ladder system for inexpensive protein molecular weight markers

被引:1
作者
Santilli, Ryan T. [1 ,2 ]
Williamson, John E., III [1 ]
Shibata, Yoshitaka [1 ,2 ]
Sowers, Rosalie P. [1 ,2 ]
Fleischman, Andrew N. [1 ,2 ,3 ]
Tan, Song [1 ]
机构
[1] Penn State Univ, Ctr Eukaryot Gene Regulat, Dept Biochem & Mol Biol, University Pk, PA 16802 USA
[2] Penn State Univ, Schreyer Honors Coll, University Pk, PA 16802 USA
[3] Thomas Jefferson Univ, 111 South 11th St,Suite 8490 Gibbon, Philadelphia, PA 19107 USA
关键词
ESCHERICHIA-COLI; EXPRESSION;
D O I
10.1038/s41598-021-96051-x
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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.
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页数:10
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