Effects of a modified dye-labeled nucleotide spacer arm on incorporation by thermophilic DNA polymerases

被引:23
作者
Lacenere, CJ
Garg, NK
Stoltz, BM
Quake, SR
机构
[1] Stanford Univ, Dept Bioengn, Stanford, CA 94305 USA
[2] CALTECH, Dept Appl Phys, Pasadena, CA 91125 USA
[3] CALTECH, Div Biol, Pasadena, CA 91125 USA
[4] CALTECH, Div Chem & Chem Engn, Pasadena, CA 91125 USA
基金
美国国家卫生研究院;
关键词
DNA polymerase; fluorescent nucleotide; sequencing by synthesis;
D O I
10.1080/15257770500377714
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The ability of eight commercially available thermophilic DNA polymerases to sequentially incorporate fluorescently labeled nucleotides sequentially was analyzed by a gel based primer extension assay. Cy5-dUTP or a variant nucleotide in which the linker had been lengthened by 14 atoms between the dye and the nucleobase were compared. We found that the Cy5-dUTP with a longer linker resulted in longer primer extension lengths. Furthermore, some of the assayed polymerases are capable of extending the primer to the full or near full length of 30 nucleotides using dye-labeled nucleotides exclusively.
引用
收藏
页码:9 / 15
页数:7
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