LIGHT-GENERATED OLIGONUCLEOTIDE ARRAYS FOR RAPID DNA-SEQUENCE ANALYSIS

被引:1024
作者
PEASE, AC [1 ]
SOLAS, D [1 ]
SULLIVAN, EJ [1 ]
CRONIN, MT [1 ]
HOLMES, CP [1 ]
FODOR, SPA [1 ]
机构
[1] AFFYMAX RES INST,PALO ALTO,CA 94304
关键词
SEQUENCING BY HYBRIDIZATION; COMBINATORIAL CHEMISTRY; DNA DIAGNOSTICS;
D O I
10.1073/pnas.91.11.5022
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
In many areas of molecular biology there is a need to rapidly extract and analyze genetic information; however, current technologies for DNA sequence analysis are slow and labor intensive. We report here how modern photolithographic techniques can be used to facilitate sequence analysis by generating miniaturized arrays of densely packed oligonucleotide probes. These probe arrays, or DNA chips, can then be applied to parallel DNA hybridization analysis, directly yielding sequence information. In a preliminary experiment, a 1.28 x 1.28 cm array of 256 different octanucleotides was produced in 16 chemical reaction cycles, requiring 4 hr to complete. The hybridization pattern of fluorescently labeled oligonucleotide targets was then detected by epifluorescence microscopy. The fluorescence signals from complementary probes were 5-35 times stronger than those with single or double base-pair hybridization mismatches, demonstrating specificity in the identification of complementary sequences. This method should prove to be a powerful tool for rapid investigations in human genetics and diagnostics, pathogen detection, and DNA molecular recognition.
引用
收藏
页码:5022 / 5026
页数:5
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