Murakami A, Tada J, Yamagata K, Takano J
Central Research Laboratory, Shimadzu Corporation, Nakagyoku, Japan.
Nucleic Acids Res. 1989 Jul 25;17(14):5587-95. doi: 10.1093/nar/17.14.5587.
In order to develop non-radioactive oligonucleotide derivatives and to examine their utility as a diagnostic tool, namely as DNA-probe, an enzyme-linked oligonucleotide was synthesized. Oligonucleotide complementary to M13mp8 phage DNA was linked to alkaline phosphatase via a crosslinker and a spacer. M13mp8 phage DNA (single strand) immobilized on the nitrocellulose membrane was hybridized with the enzyme-linked oligonucleotide. The hybrid was detected with three detection methods; (1)colorimetric detection in solution, (2)colorimetric one on membranes, and (3)fluorometric one in solution. Methods(2) and (3) gave high sensitivities to detect as low as several to several tens attomoles of DNA and it was found that those methods with enzyme-linked oligonucleotides are potent for DNA-probe methodology from the viewpoint of automation.
为了开发非放射性寡核苷酸衍生物并检验其作为诊断工具(即作为DNA探针)的效用,合成了一种酶联寡核苷酸。与M13mp8噬菌体DNA互补的寡核苷酸通过交联剂和间隔基与碱性磷酸酶相连。固定在硝酸纤维素膜上的M13mp8噬菌体DNA(单链)与酶联寡核苷酸杂交。用三种检测方法检测杂交体:(1)溶液中的比色检测,(2)膜上的比色检测,以及(3)溶液中的荧光检测。方法(2)和(3)具有高灵敏度,能够检测低至几到几十阿托摩尔的DNA,并且发现从自动化的角度来看,那些使用酶联寡核苷酸的方法在DNA探针方法学中很有效。