Development of mass spectrometry for rapid detection of DNA fragments
Conference
·
OSTI ID:559852
- Oak Ridge National Lab., TN (United States)
Identifying the presence of a specific DNA fragment is becoming increasingly critical in medicine, law enforcement, consumer safety, and other applications. Regions in DNA that are diagnostic for a targeted genetic disease, individual, or microorganism are amplified using the Polymerase Chain Reaction (PCR) or other reactions. These products, which contain a specific number of nucleotide units, are currently analyzed by electrophoresis or hybridization. Mass spectrometry has the potential of characterizing the PCR products faster and more confidently than these methods. We have been investigating matrix assisted laser desorption/ionization (MALDI) mass spectrometry for the detection of DNA fragments, with the goal of developing an analytical method that can be used to screen many samples quickly and reliably. We have demonstrated the efficacy of this approach by detecting PCR products isolated from both human and microbial samples. We are currently investigating approaches for improving sample preparation, enhancing ionization, extending mass range, and increasing mass resolution.
- OSTI ID:
- 559852
- Report Number(s):
- CONF-970443--
- Country of Publication:
- United States
- Language:
- English
Similar Records
Molecular diagnostics via mass spectrometry of PCR-amplified DNA products
Rapid mass spectrometric DNA diagnostics for assessing microbial community activity during bioremediation. 1997 annual progress report
Fast DNA analysis by laser mass spectrometry for human genome analysis
Conference
·
Sat Dec 30 23:00:00 EST 1995
·
OSTI ID:210617
Rapid mass spectrometric DNA diagnostics for assessing microbial community activity during bioremediation. 1997 annual progress report
Technical Report
·
Tue Dec 31 23:00:00 EST 1996
·
OSTI ID:13428
Fast DNA analysis by laser mass spectrometry for human genome analysis
Journal Article
·
Fri Mar 31 23:00:00 EST 1995
· AIP Conference Proceedings
·
OSTI ID:76384