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用带有大体积荧光团的正交离子配对反相液相色谱法纯化寡核苷酸。

Orthogonal ion pairing reversed phase liquid chromatography purification of oligonucleotides with bulky fluorophores.

机构信息

Roche Molecular Diagnostics, 4300 Hacienda Drive, Pleasanton, CA 94588, USA.

出版信息

J Chromatogr A. 2014 Feb 14;1329:78-82. doi: 10.1016/j.chroma.2013.12.072. Epub 2014 Jan 10.

Abstract

A dual labeled oligonucleotide used as TaqMan® or 5' nuclease probe for in vitro diagnostic has been purified through orthogonal ion-pairing reversed phase chromatography, using polymeric semi-preparative and preparative PRP-1 column. We studied the mechanism of separation of oligonucleotides using ion-pairing reversed phase chromatography. We found that elution profiles of dye labeled oligonucleotides can be controlled by use of specific ion-pairing reagents. Here, we report a method for purification of an oligonucleotide containing an internally positioned rhodamine dye using two orthogonal chromatographic steps, in which the primary step resolves mostly by differences in hydrophobicity by using a weak ion-pairing reagent, and a secondary step uses a strong ion-pairing reagent for separation of length variants. Purification is demonstrated for both 1 and 15μmol scale syntheses, and amenable to further scale up for commercial lot production.

摘要

一种双标记寡核苷酸,用作 TaqMan®或 5'核酸酶探针,用于体外诊断,已通过正交离子对反相色谱法,使用聚合半制备和制备 PRP-1 柱进行纯化。我们研究了使用离子对反相色谱法分离寡核苷酸的机制。我们发现,使用特定的离子对试剂可以控制染料标记寡核苷酸的洗脱曲线。在这里,我们报告了一种使用两种正交色谱步骤纯化含有内部定位罗丹明染料的寡核苷酸的方法,其中主要步骤主要通过使用弱离子对试剂的疏水性差异来区分,而次要步骤使用强离子对试剂来分离长度变体。已针对 1μmol 和 15μmol 规模的合成进行了纯化,并且可进一步放大规模以用于商业批量生产。

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