GENOME SEQUENCING VIA ION TRAP/TIME-OF-FLIGHT MASS SPEC
Project Number2R01HG000685-03
Former Number1R01HG001301-01
Contact PI/Project LeaderLUBMAN, DAVID M.
Awardee OrganizationUNIVERSITY OF MICHIGAN AT ANN ARBOR
Description
Abstract Text
DESCRIPTION (Adapted from Investigator's Abstract): Dr. Lubman proposes
to develop new methodology for the rapid sequencing of DNA, involving
a combination of biochemical methods and mass analysis via the ion trap
storage/reflection time-of-flight hybrid mass spectrometer. The method
will involve using mass analysis to sequence the DNA fragments produced
by the Sanger method rather than gel electrophoretic techniques. The
sequence is encoded in the mass of the DNA strands produced, which can
be rapidly separated and identified based upon electrostatic acceleration
in a time-of-flight device. Using this methodology it is estimated that
at least 50 kbases can be sequenced per day with a desired ultimate goal
of 200 kbases per day. This sequencing rate will be based upon matrix-
assisted laser desorption/ionization (MALDI) of DNA strands of at least
200 base pairs which can be mass resolved and identified and a
multisample desorption probe which will provide rapid sample throughput.
The MALDI process will involve using 3- hydroxypicolinic acid on a Nafion
polymer substrate for vaporization and ionization of intact DNA strands.
In order to enhance the sensitivity of the method to detect the low
femtomolar levels of each DNA strand available from biochemical
degradation, ion trap storage technology has been interfaced to a
reflectron time-of-flight device to allow integration of the signal over
multiple laser pulses. In addition, the ion trap storage method has been
shown to be essential for attaining enhanced resolution and for
minimizing metastable decomposition for the highly energetic ions
produced by the MALDI process. Further development of the ion
trap/reTOF for storage and analysis of the high mass range required for
DNA will be proposed as part of this work. This will involve the use of
low frequency RF on the ring electrode and various modifications to the
trap and reTOF designs. Ultimately, additional methods for
volatilization and ionization of DNA using MALDI from liquid or solid
doped matrices will be studied and optimized for these experiments in
order to enhance the analytical throughput.
Public Health Relevance Statement
Data not available.
NIH Spending Category
No NIH Spending Category available.
Project Terms
DNAbiomedical equipment developmentelectrospray ionization mass spectrometrygas chromatography mass spectrometrymass spectrometrynucleic acid sequence
No Sub Projects information available for 2R01HG000685-03
Publications
Publications are associated with projects, but cannot be identified with any particular year of the project or fiscal year of funding. This is due to the continuous and cumulative nature of knowledge generation across the life of a project and the sometimes long and variable publishing timeline. Similarly, for multi-component projects, publications are associated with the parent core project and not with individual sub-projects.
No Publications available for 2R01HG000685-03
Patents
No Patents information available for 2R01HG000685-03
Outcomes
The Project Outcomes shown here are displayed verbatim as submitted by the Principal Investigator (PI) for this award. Any opinions, findings, and conclusions or recommendations expressed are those of the PI and do not necessarily reflect the views of the National Institutes of Health. NIH has not endorsed the content below.
No Outcomes available for 2R01HG000685-03
Clinical Studies
No Clinical Studies information available for 2R01HG000685-03
News and More
Related News Releases
No news release information available for 2R01HG000685-03
History
No Historical information available for 2R01HG000685-03
Similar Projects
No Similar Projects information available for 2R01HG000685-03