Brown Phyllis R, Robb Christina S, Geldart Susan E
Department of Chemistry, University of Rhode Island, Kingston 02881, USA.
J Chromatogr A. 2002 Aug 2;965(1-2):163-73. doi: 10.1016/s0021-9673(01)01561-8.
The recent mapping of the human genome was a tremendous achievement made possible to a large degree by the development of analytical methods for sequencing purine and pyrimidine bases in nucleic acids. In the last 3 decades, the number of analyses of nucleic acids and their constituents by HPLC and capillary electrophoresis (CE) has exploded. These techniques have been used not only for genomics, but also for the determination of free nucleotides, nucleosides and their bases in body fluids and tissues. Although a large number of HPLC and CE papers have been published on nucleic acid constituent applications, relatively little has been written on the mechanisms of the separations. However, to optimize analytical conditions knowledgeably and rapidly, it is important to know why and how these separations occur and the factors that affect them. The HPLC methods for the analysis of nucleic acid constituents and the information available on some of the mechanisms of separation of nucleotides, nucleosides and their bases, as well as the analysis of these compounds by CE and the factors that affect these separations are discussed.
近期人类基因组图谱的绘制是一项巨大成就,这在很大程度上得益于核酸中嘌呤和嘧啶碱基测序分析方法的发展。在过去三十年里,利用高效液相色谱法(HPLC)和毛细管电泳法(CE)对核酸及其成分进行分析的数量呈爆炸式增长。这些技术不仅用于基因组学,还用于测定体液和组织中的游离核苷酸、核苷及其碱基。尽管已经发表了大量关于核酸成分应用的HPLC和CE论文,但关于分离机制的论述相对较少。然而,为了明智且迅速地优化分析条件,了解这些分离为何以及如何发生以及影响它们的因素很重要。本文将讨论用于分析核酸成分的HPLC方法、关于核苷酸、核苷及其碱基某些分离机制的现有信息,以及通过CE对这些化合物的分析和影响这些分离的因素。