Yehle C O, Patterson W L, Boguslawski S J, Albarella J P, Yip K F, Carrico R J
Ames Division, Miles Laboratories, Inc., Elkhart, IN 46515.
Mol Cell Probes. 1987 Jun;1(2):177-93. doi: 10.1016/0890-8508(87)90026-0.
Rapid, convenient and non-isotopic nucleic-acid hybridization methods are needed for this technology to have practical use in clinical diagnostic tests. A method for hybridization of RNA with a DNA probe in solution followed by capture and measurement of the hybrid is described. DNA probes complementary to 23S rRNAs from Escherichia coli and Bacillus subtilis were labeled with a photoactivable biotin reagent. Hybridization of the biotinylated probes with rRNA was complete in less than 5 min. The resultant hybrids were allowed to bind simultaneously to succinylated avidin immobilized on latex and to beta-galactosidase-labeled Fab' fragments of a monoclonal antibody-specific for DNA:RNA. Finally, beta-galactosidase associated with the captured hybrids was measured colorimetrically. The hybridization method can detect less than 1000 bacteria per assay and has broad specificity to permit detection of the various genera of bacteria that infect the urinary tract.
为使该技术在临床诊断测试中具有实际用途,需要快速、便捷且非同位素的核酸杂交方法。本文描述了一种在溶液中使RNA与DNA探针杂交,随后捕获并检测杂交体的方法。与大肠杆菌和枯草芽孢杆菌的23S rRNA互补的DNA探针用可光活化的生物素试剂进行标记。生物素化探针与rRNA的杂交在不到5分钟内即可完成。使所得杂交体同时与固定在乳胶上的琥珀酰化抗生物素蛋白以及对DNA:RNA具有特异性的单克隆抗体的β-半乳糖苷酶标记的Fab'片段结合。最后,通过比色法测定与捕获的杂交体相关的β-半乳糖苷酶。该杂交方法每次检测可检测到少于1000个细菌,并且具有广泛的特异性,能够检测出感染尿道的各种细菌属。