Simultaneous detection of diverse analytes with an aptazyme ligase array

被引:50
|
作者
Hesselberth, JR [1 ]
Robertson, MP [1 ]
Knudsen, SM [1 ]
Ellington, AD [1 ]
机构
[1] Univ Texas, Inst Mol & Cellular Biol, Dept Chem & Biochem, Austin, TX 78712 USA
关键词
allosteric ribozyme; aptazyme; array; aptamer; in vitro selection; SELEX;
D O I
10.1016/S0003-2697(02)00441-4
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Allosteric ribozymes (aptazymes) can transduce the noncovalent recognition of analytes into the catalytic generation of readily observable signals. Aptazymes are easily engineered, can detect diverse classes of biologically relevant molecules, and have high signal-to-noise ratios. These features make aptazymes useful candidates for incorporation into biosensor arrays. Allosteric ribozyme ligases that can recognize a variety of analytes ranging from small organics to proteins have been generated. Upon incorporation into an array format, multiple different aptazyme ligases were able to simultaneously detect their cognate analytes with high specificity. Analyte concentrations could be accurately measured into the nanomolar range. The fact that analytes induced the formation of new covalent bonds in aptazyme ligases (as opposed to noncovalent bonds in antibodies) potentiated stringent washing of the array, leading to improved signal-to-noise ratios and limits of detection. (C) 2003 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:106 / 112
页数:7
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