DNA molecules are a natural substrate for fluidic manipulations given their enormous persistence length (approximately 500 angstroms), and intrinsic girth--a typical human chromosome contains a DNA molecule that spans about 1 inch, and forms a random coil with dimensions approaching approximately 10 mm. Given these physical properties, microfluidic devices will be easily engineered to elongate chains or direct their deposition onto surfaces for further analysis.
The aim of this proposed research to fabricate, evaluate, and employ new devices based on recent insights drawn from sophisticated simulation studies of the dynamics of large DNA molecules within confined environments typified by micro and nanofluidic devices. New PDMS devices will feature a combination of nano approaches to molecular confinement combined with the simplicity of microscale devices to engender these new findings within a high-throughput, single molecule environment. Proven high-throughput single molecule analysis systems will be employed and extended to guide this development through the creation of statistically meaningful datasets with aims devoted to the development of new modalities for studying single molecule biochemistries. These new systems will be applied to transcriptional studies, and new approaches for the in vitro construction of very large single DNA molecule constructs. Together these new technologies bode well for the future of personalized medicine through the analysis of whole genome over large populations

Agency
National Institute of Health (NIH)
Institute
National Human Genome Research Institute (NHGRI)
Type
Research Project (R01)
Project #
5R01HG000225-11
Application #
6902575
Study Section
Genome Study Section (GNM)
Program Officer
Schloss, Jeffery
Project Start
1991-01-01
Project End
2007-04-30
Budget Start
2005-05-01
Budget End
2006-04-30
Support Year
11
Fiscal Year
2005
Total Cost
$501,821
Indirect Cost
Name
University of Wisconsin Madison
Department
Miscellaneous
Type
Other Domestic Higher Education
DUNS #
161202122
City
Madison
State
WI
Country
United States
Zip Code
53715
Krerowicz, Samuel J W; Hernandez-Ortiz, Juan P; Schwartz, David C (2018) Microscale Objects via Restructuring of Large, Double-Stranded DNA Molecules. ACS Appl Mater Interfaces :
Kounovsky-Shafer, Kristy L; Hernandez-Ortiz, Juan P; Potamousis, Konstantinos et al. (2017) Electrostatic confinement and manipulation of DNA molecules for genome analysis. Proc Natl Acad Sci U S A 114:13400-13405
Lequieu, Joshua; Schwartz, David C; de Pablo, Juan J (2017) In silico evidence for sequence-dependent nucleosome sliding. Proc Natl Acad Sci U S A 114:E9197-E9205
Lequieu, Joshua; Córdoba, Andrés; Schwartz, David C et al. (2016) Tension-Dependent Free Energies of Nucleosome Unwrapping. ACS Cent Sci 2:660-666
Li, Yang; Zhou, Shiguo; Schwartz, David C et al. (2016) Allele-Specific Quantification of Structural Variations in Cancer Genomes. Cell Syst 3:21-34
Mendelowitz, Lee M; Schwartz, David C; Pop, Mihai (2016) Maligner: a fast ordered restriction map aligner. Bioinformatics 32:1016-22
Park, Dong-Wook; Kim, Hyungsoo; Bong, Jihye et al. (2016) Flexible bottom-gate graphene transistors on Parylene C substrate and the effect of current annealing. Appl Phys Lett 109:152105
Lee, Seonghyun; Oh, Yeeun; Lee, Jungyoon et al. (2016) DNA binding fluorescent proteins for the direct visualization of large DNA molecules. Nucleic Acids Res 44:e6
Zhou, Shiguo; Goldstein, Steve; Place, Michael et al. (2015) A clone-free, single molecule map of the domestic cow (Bos taurus) genome. BMC Genomics 16:644
Hernández-Ortiz, Juan P; de Pablo, Juan J (2015) Self-consistent description of electrokinetic phenomena in particle-based simulations. J Chem Phys 143:014108

Showing the most recent 10 out of 60 publications