Suppr超能文献

通过基质辅助激光解吸/电离飞行时间质谱法分析酶促DNA测序反应。

Analysis of enzymatic DNA sequencing reactions by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry.

作者信息

Shaler T A, Tan Y, Wickham J N, Wu K J, Becker C H

机构信息

Molecular Physics Laboratory, SRI International, Menlo Park, CA 94025, USA.

出版信息

Rapid Commun Mass Spectrom. 1995;9(10):942-7. doi: 10.1002/rcm.1290091015.

Abstract

The products from base-specific, dideoxy-nucleotide chain-termination DNA sequencing reactions catalyzed by the modified T7 DNA polymerase have been analyzed by using the technique of matrix-assisted laser desorption/ionization (MALDI) time-of-flight mass spectrometry. Preliminary experiments were performed to determine detection limits for a synthetic mixture of mixed-base single-stranded DNA which contained a 14-mer, a 21-mer, and a 41-mer; acceptable spectra, showing peaks for each component, were obtainable for samples that contained as little as 5 fmol per component. Initial sequencing reactions were therefore carried out on 2-pmol amounts of a short synthetic template that was 45 nucleotides in length, employing 2 pmol of 12-mer as the primer strand. This provided readable sequence information out to the 19th base past the primer. Using a 21-mer primer, nearly the entire sequence of the template could be read.

摘要

利用基质辅助激光解吸/电离(MALDI)飞行时间质谱技术,对经修饰的T7 DNA聚合酶催化的碱基特异性双脱氧核苷酸链终止DNA测序反应产物进行了分析。进行了初步实验,以确定含有14聚体、21聚体和41聚体的混合碱基单链DNA合成混合物的检测限;对于每种成分低至5 fmol的样品,可获得显示各成分峰的可接受光谱。因此,最初的测序反应是在2 pmol长度为45个核苷酸的短合成模板上进行的,使用2 pmol的12聚体作为引物链。这提供了可读的序列信息,直至引物后的第19个碱基。使用21聚体引物,可以读取模板几乎整个序列。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验