Affinity purification of plasmid DNA by temperature-triggered precipitation

被引:20
作者
Kostal, J [1 ]
Mulchandani, A [1 ]
Chen, W [1 ]
机构
[1] Univ Calif Riverside, Dept Environm Chem & Engn, Riverside, CA 92521 USA
关键词
DNA cloning; plasmid binding; plasmid purification; affinity precipitation; elastin-like proteins (ELPs);
D O I
10.1002/bit.10890
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
This report describes a new plasmid DNA purification method, which takes advantage of the DNA-binding affinity and specificity of the bacterial metalloregulatory protein MerR, and of the temperature responsiveness of elastin-like proteins (ELPs). Upon increasing the temperature, ELP undergoes a reversible phase transition from water-soluble forms into aggregates, and this property was exploited for the precipitation of plasmid DNA containing the MerR recognition sequence by a simple temperature trigger. In one purification step, plasmid DNA was purified from E. coli cell lysates to a better purity than that prepared by a standard alkaline purification method, with no contaminating chromosomal DNA and cellular proteins. This protein-based approach, in combination with the reversible phase transition feature of ELP, makes the outlined method a promising candidate for large-scale purification of plasmid DNA for sensitive applications such as nonviral gene therapy or DNA vaccines. (C) 2004 Wiley Periodicals, Inc.
引用
收藏
页码:293 / 297
页数:5
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