Design and fabrication of microwell array chips for a solution-based, photogenerated acid-catalyzed parallel oligonuclotide DNA synthesis

被引:12
|
作者
Srivannavit, O
Gulari, M
Gulari, E [1 ]
LeProust, E
Pellois, JP
Gao, XL
Zhou, XC
机构
[1] Univ Michigan, Dept Chem Engn, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Dept Elect Engn, Ann Arbor, MI 48109 USA
[3] Univ Houston, Dept Chem, Houston, TX 77004 USA
[4] Atact Technol Inc, Houston, TX 77030 USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
oligonucleotide DNA microarray; micromachining; microwell; photogenerated acid;
D O I
10.1016/j.sna.2004.04.025
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
Development of synthesis methods using high yield acid-labile rather than photolabile group protected monomers is desirable to produce microarrays of superior quality, general adaptability and reduced cost of genetic research. However, using solution photochemistry for acid-labile deprotection requires the reaction sites being isolated from each other to prevent diffusion of reagents during a photolytic reaction. We present fabrication methods of two types of microwell array chips with different isolation strategies for carrying out parallel oligonucleotide DNA (oDNA) synthesis in the liquid phase: electroplated microwell array chips with an isolation wall and a mechanical sealing, and etched patterned microwell array chips with surface tension isolation. Both surface and bulk micromachining technologies were used for fabrication of those chips. We also discuss various problems regarding fabrication and use. The validated fidelity from the single mismatch detection of oligonucleotide DNA microwell array chips is also given to prove successful isolation of the liquid during a photolytic reaction. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:150 / 160
页数:11
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