Solid-phase cloning for high-throughput assembly of single and multiple DNA parts

被引:12
作者
Lundqvist, Magnus [1 ]
Edfors, Fredrik [1 ]
Sivertsson, Asa [1 ]
Hallstrom, Bjorn M. [1 ]
Hudson, Elton P. [2 ]
Tegel, Hanna [1 ]
Holmberg, Anders [1 ]
Uhlen, Mathias [1 ,2 ,3 ]
Rockberg, Johan [1 ]
机构
[1] KTH Royal Inst Technol, AlbaNova Univ Ctr, Sch Biotechnol, S-10691 Stockholm, Sweden
[2] KTH Royal Inst Technol, Sci Life Lab, S-17165 Stockholm, Sweden
[3] Tech Univ Denmark, Novo Nordisk Fdn Ctr Biosustainabil, DK-2970 Horsholm, Denmark
关键词
MAGNETIC BEADS; PCR; PROTEIN; POLYMERASE; CONSTRUCTION; EXPRESSION; MOLECULES; EMULSION;
D O I
10.1093/nar/gkv036
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We describe solid-phase cloning (SPC) for high-throughput assembly of expression plasmids. Our method allows PCR products to be put directly into a liquid handler for capture and purification using paramagnetic streptavidin beads and conversion into constructs by subsequent cloning reactions. We present a robust automated protocol for restriction enzyme based SPC and its performance for the cloning of >60 000 unique human gene fragments into expression vectors. In addition, we report on SPC-based single-strand assembly for applications where exact control of the sequence between fragments is needed or where multiple inserts are to be assembled. In this approach, the solid support allows for head-to-tail assembly of DNA fragments based on hybridization and polymerase fill-in. The usefulness of head-to-tail SPC was demonstrated by assembly of >150 constructs with up to four DNA parts at an average success rate above 80%. We report on several applications for SPC and we suggest it to be particularly suitable for high-throughput efforts using laboratory workstations.
引用
收藏
页数:11
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