Progress in gene assembly from a MAS-driven DNA microarray

被引:11
作者
Kim, C.
Kaysen, J.
Richmond, K.
Rodesch, M.
Binkowski, B.
Chu, L.
Li, M.
Heinrich, K.
Blair, S.
Belshaw, P.
Sussman, M.
Cerrina, F. [1 ]
机构
[1] Univ Wisconsin, Ctr Nanotechnol, Madison, WI 53706 USA
[2] Univ Wisconsin, Ctr Biotechnol, Madison, WI 53706 USA
[3] Univ Wisconsin, Dept Elect & Comp Engn, Madison, WI 53706 USA
[4] Univ Wisconsin, Dept Chem, Madison, WI 53706 USA
[5] Univ Wisconsin, Dept Biochem, Madison, WI 53706 USA
基金
美国国家卫生研究院;
关键词
maskless array synthesizer; image locking; inverse capping; gene assembly; DNA microarray; sequence error prevention/correction; smGFP assembly; MutS filtering; consensus shuffling;
D O I
10.1016/j.mee.2006.01.143
中图分类号
TM [电工技术]; TN [电子技术、通信技术];
学科分类号
0808 ; 0809 ;
摘要
We report the progress on 765 bp full green fluorescent protein (GFP) gene assembly of oligonucleotides from a single DNA microarray, using the amplification and assembly of chip-eluted DNA (AACED) strategy. The chip was fabricated with maskless array synthesizer (MAS) via 2-nitrophenylpropoxycarbonyl (NPPOC)-driven light-directed synthesis. Upon the recognition of the strong dependence of final assembly yield on the purity of construct oligonucleotides, we put a large effort in developing error reduction methods with a considerable improvement in the purity of chip-oligonucleotides in terms of exposure image quality, synthesis protocols and mask design. In addition to the synthesis improvement (as an error prevention), a post-assembly error filtering method was devised and developed-consensus shuffling using MutS-protein filtering. The preliminary demonstrations indicate their potential uses in more rapid and efficient DNA assembly process. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:1613 / 1616
页数:4
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