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用于多重生物测定的组合荧光能量转移标签。

Combinatorial fluorescence energy transfer tags for multiplex biological assays.

作者信息

Tong A K, Li Z, Jones G S, Russo J J, Ju J

机构信息

Laboratory of DNA Sequencing and Chemical Biology, Columbia Genome Center, Columbia University College of Physicians and Surgeons, New York, NY 10032, USA.

出版信息

Nat Biotechnol. 2001 Aug;19(8):756-9. doi: 10.1038/90810.

Abstract

We report an approach for developing combinatorial fluorescence energy transfer (CFET) tags by tuning the tags' fluorescence emission signatures. The tags can all be excited at a single wavelength and analyzed by a simple optical system. We constructed eight CFET tags with unique fluorescence signatures, detected by a three-color capillary array electrophoresis (CAE) system with 488 nm excitation, using only three fluorescent dyes. A 1',2'-dideoxyribose phosphate spacer was used to separate the donor and acceptor to tune the energy transfer efficiency, generating unique fluorescence signatures. The spacer also served as an electrophoretic mobility tag to tune the mobility of CFET-labeled DNA for multiplex detection of single-nucleotide polymorphisms (SNPs). Six nucleotide variations were identified simultaneously using six CFET tags on synthetic DNA templates and on a PCR product from the retinoblastoma tumor suppressor gene.

摘要

我们报告了一种通过调整组合荧光能量转移(CFET)标签的荧光发射特征来开发此类标签的方法。这些标签都可以在单一波长下激发,并通过一个简单的光学系统进行分析。我们构建了八个具有独特荧光特征的CFET标签,仅使用三种荧光染料,通过488 nm激发的三色毛细管阵列电泳(CAE)系统进行检测。使用1',2'-二脱氧核糖磷酸间隔物来分离供体和受体,以调整能量转移效率,从而产生独特的荧光特征。该间隔物还用作电泳迁移率标签,以调整CFET标记的DNA的迁移率,用于单核苷酸多态性(SNP)的多重检测。在合成DNA模板和视网膜母细胞瘤肿瘤抑制基因的PCR产物上,使用六个CFET标签同时鉴定了六个核苷酸变异。

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