期刊
MOLECULAR BIOTECHNOLOGY
卷 40, 期 2, 页码 119-126出版社
HUMANA PRESS INC
DOI: 10.1007/s12033-008-9096-x
关键词
phosphorothioate; primer; stereochemistry; PCR; DNA polymerase; single base extension; P-chirality; exonuclease; chemical synthesis; stereocontrolled synthesis; oxathiaphospholane synthesis; diastereomers; PS-oligonucleotide
资金
- Ministry of Science and Higher Education
- Polish Academy of Sciences [70/E-63/SN-014/2006, PBZ-MNiSW-07/I/2007]
Influence of stereochemistry of the 3'-terminal phosphorothioate (PS)-modified primers was studied in a single base extension (SBE) assay to evaluate any improvements in specificity. SBE reactions were catalyzed by members of the high fidelity Pfu family of DNA polymerases with (exo+) or without (exo-) 3' -> 5' exonucleolytic activity. The diastereomerically pure PS-labeled primers used in these studies were obtained either by the stereospecific chemical synthesis invented in our laboratory or by the more conventional ion-exchange chromatographic method for separation of a mixture of diastereomers (R-P and S-P). When the SBE reaction was performed in the presence of mispaired 2'-deoxyribonucleoside triphosphates (dNTPs), the racemic 3'-phosphorothioate primer mixture resulted in a lower level of 3' -> 5' exonuclease-mediated cleavage products in comparison to the SBE reactions carried out with the corresponding unmodified primer. When the diastereomerically pure R-P 3'-phosphorothioate primer was examined, the results were largely the same as for the racemic 3'-phosphorothioate primer mixture. In contrast, a 3'-PS primer of S-P configuration displayed significantly improved performance in the SBE reaction. This included the lack of 3' -> 5' proofreading products, less mispriming, and improved yield of incorporation of the correct nucleotide.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据