A novel fluorescent method for detection of subpicogram quantities of nucleic acids
| Project/Area Number |
02559002
|
|---|
| Research Category |
Grant-in-Aid for Developmental Scientific Research (B)
|
| Allocation Type | Single-year Grants |
|---|
| Research Field |
広領域
|
|---|
| Research Institution | Hokkaido University |
|---|
Principal Investigator |
HORI Hiroshi Hokkaido University Science Synthesis of Coumarin and Perylene derivatives, 理学部, 教授 (40000814)
|
|---|
| Co-Investigator(Kenkyū-buntansha) |
YOSHIDA Kiyohito Hokkaido University Science Synthesis of Naphthol derivatives, 理学部, 助手 (40210687)
YOSHIDA Michihiro Hokkaido University Science Screening, 理学部, 教授 (60001765)
SHIRAHAMA Haruhisa Hokkaido University Science Instruction in synthesis, 理学部, 教授 (00000802)
高木 信夫 北海道大学, 遺伝子実験施設, 助教授 (20001852)
|
|---|
| Project Period (FY) |
1990 – 1991
|
| Project Status |
Completed (Fiscal Year 1991)
|
| Budget Amount *help |
¥6,700,000 (Direct Cost: ¥6,700,000)
Fiscal Year 1991: ¥2,600,000 (Direct Cost: ¥2,600,000)
Fiscal Year 1990: ¥4,100,000 (Direct Cost: ¥4,100,000)
|
|---|
| Keywords | Detection of nucleic acid / Non-RI / Fluorescent substrate |
|---|
| Research Abstract |
In recombinant DNA techniques, it is required to detect a very small amount of nucleic acids. In standard protocols this is accomplished by the use of radio-labeled nucleic acids as probes. However, the inherent drawbacks of radiolabeled probes, such as chemical lability due to radiolytic decomposition, personnel safety and disposal problems, short half-life and duration of autoradiographic exposure limit the usefulness of radio-labeled probes in conventional laboratories. It is therefore desirable to have sensitive, non-radioisotope methods for detecting nucleic acids. Recontly, efforts have been made in a number of laboratories to innovate a new non-radioisotopic methods and a variety of methods have been proposed. Among these, the Boehringer's Digoxigenin-alkaline phosphosphatase method utilizing either BCIP-Nitro BT or a chemiluminescent substrate, AMPPD as a substrate appears to be most reliable and sensitive method. However, the method is still lower in sensitivity than the RI method. To improve the sensitivity of thenon-RI method, we have attempted in this profect to synthesize fluorogenic substrates for alkalien phosphatase which upon hydrolysis yield insoluble, highly fluorescent products. As a result, HNPP (3-hydroxy-N-2-biphenylyl-2-naphthalenecarboxamide phosphate) was found to be the most useful substrate among a total of 86 fluorochromes synthesized. With this substrate, it is possible to detact as small as 10fg of DNA by spot tests, and 70fg of DNA by southern blots. The method ustilizing HNPP is superior to any available techniques with respect to resolution, speed, ease of reaction monitoring, data storage, reprobing and stability of reagents.
|
Report
(3 results)
Research Products
(3 results)
