Berti L, Xie J, Medintz I L, Glazer A N, Mathies R A
Department of Chemistry, University of California, Berkeley 94720, USA.
Anal Biochem. 2001 May 15;292(2):188-97. doi: 10.1006/abio.2001.5069.
Fluorescence energy transfer (ET) primers and terminators are the reagents of choice for multiplex DNA sequencing and analysis. We present here the design, synthesis and evaluation of a four-color set of ET cassettes, fluorescent labeling reagents that can be quantitatively coupled to a thiol-activated target through a disulfide exchange reaction. The ET cassette consists of a sugar-phosphate spacer with a FAM donor at the 3'-end, an acceptor linked to a modified T-base at the 5'-end of the spacer and a mixed disulfide for coupling to a thiol at the 5'-end. The acceptor dye emission intensities of ET labeled primers produced in this manner are comparable to commercial ET primers. The utility of our ET cassette-labeled primers is demonstrated by performing four-color capillary electrophoresis sequencing with the M13(-21)forward primer and by generating and analyzing a set of single-nucleotide-polymorphism-specific PCR amplicons.
荧光能量转移(ET)引物和终止剂是多重DNA测序和分析的首选试剂。我们在此展示了一组四色ET盒的设计、合成和评估,这些荧光标记试剂可通过二硫键交换反应定量偶联到硫醇活化的靶标上。ET盒由一个在3'端带有FAM供体的糖磷酸间隔区、一个连接到间隔区5'端修饰T碱基的受体以及一个用于在5'端偶联硫醇的混合二硫键组成。以这种方式产生的ET标记引物的受体染料发射强度与商业ET引物相当。通过使用M13(-21)正向引物进行四色毛细管电泳测序,以及生成和分析一组单核苷酸多态性特异性PCR扩增子,证明了我们的ET盒标记引物的实用性。