Mansfield E S, Worley J M, McKenzie S E, Surrey S, Rappaport E, Fortina P
Molecular Dynamics, Inc., Sunnyvale, CA, USA.
Mol Cell Probes. 1995 Jun;9(3):145-56. doi: 10.1006/mcpr.1995.0023.
Nucleic acid probe-based assays are now widely used in genetic research, human identification, forensics and in a broad spectrum of clinical assays in the fields of microbiology, haematology/oncology and virology. Labelled probes are used in a variety of assay formats including dot-blots, Southern blots (DNA target), Northern blots (RNA target), Western blots (protein target), in situ hybridization, plaque or colony screening and immobilized arrays on silicon or glass surfaces. Traditionally, the probes used in these assays have a radioactive 32phosphorous label that has a short shelf-life, is dangerous, has high disposal costs and, when labelled to high specific-activity, may be unstable. Extensive efforts to develop alternative labelling techniques have resulted in colorimetric, chemiluminescent and fluorescent assay formats. This review summarizes the properties desired in a probe, describes the advantages and disadvantages of the different non-radioactive labelling strategies, and illustrates examples of probe-based assays in which detection is facilitated by imaging samples using a general purpose fluorescence scanner.
基于核酸探针的检测方法目前广泛应用于基因研究、人类身份鉴定、法医学以及微生物学、血液学/肿瘤学和病毒学等广泛领域的临床检测中。标记探针用于多种检测形式,包括斑点印迹、Southern印迹(DNA靶标)、Northern印迹(RNA靶标)、Western印迹(蛋白质靶标)、原位杂交、噬菌斑或菌落筛选以及硅或玻璃表面的固定化阵列。传统上,这些检测中使用的探针带有放射性32磷标记,其保质期短、危险、处置成本高,并且当标记到高比活度时可能不稳定。开发替代标记技术的大量努力已产生了比色、化学发光和荧光检测形式。本综述总结了探针所需的特性,描述了不同非放射性标记策略的优缺点,并举例说明了基于探针的检测方法,其中使用通用荧光扫描仪对样品进行成像有助于检测。