Oser A, Roth W K, Valet G
Mildred-Scheel-Labor für Krebszellforschung, Martinsried, FRG.
Nucleic Acids Res. 1988 Feb 11;16(3):1181-96. doi: 10.1093/nar/16.3.1181.
A new labelling method for cloned DNA probes used in hybridization assays is described. The DNA insert of recombinant plasmid DNA was made partially single-stranded for the labelling reaction by a restriction enzyme digest, followed by a controlled exonuclease III incubation. A thiol-containing psoralen derivative was covalently bound through irradiation with UV-light to the remaining double-stranded region of the plasmid DNA. The psoralen-SH groups were labelled with a large number of metal chelators (diethylentriamine pentaacetic acid, DTPA) using poly-L-lysine as a macromolecular carrier. The main advantage of the labelling procedure is that a high degree of labelling is achieved without modification of the single-stranded DNA hybridizing sequences. The specific hybrids were labelled after filter hybridization with europium ions through the chelating groups of DTPA. The europium ions were quantitatively detected by time-resolved fluorometry. The sensitivity of the assay for target DNA detection was in the low picogram range, comparable to radioactively labelled DNA probes.
本文描述了一种用于杂交分析的克隆DNA探针的新标记方法。通过限制性内切酶消化使重组质粒DNA的DNA插入片段部分单链化,用于标记反应,随后进行受控的核酸外切酶III孵育。通过紫外线照射,将含硫醇的补骨脂素衍生物共价结合到质粒DNA的剩余双链区域。使用聚-L-赖氨酸作为大分子载体,用大量金属螯合剂(二乙三胺五乙酸,DTPA)标记补骨脂素-SH基团。标记过程的主要优点是在不修饰单链DNA杂交序列的情况下实现了高度标记。通过DTPA的螯合基团与铕离子进行滤膜杂交后,特异性杂交体被标记。通过时间分辨荧光法对铕离子进行定量检测。用于检测靶DNA的分析方法的灵敏度在低皮克范围内,与放射性标记的DNA探针相当。