Single-molecule approaches can be used to achieve a fundamental understanding of biological processes occurring at the nanometer (nm) scale, in the millisecond (ms) time domain and at the piconewton (pN) force level. In this study, we will develop novel uses of single-pair Fluorescence Resonance Energy Transfer (spFRET), Magnetic Tweezers (MT) and combination instruments for the analysis of DNA-structure specific helicases, essential motor proteins for life. We will develop combination scanning confocal fluorescence microscope/magnetic tweezers (SCFM/MT) to study interactions between helicase and helicase-protein complexes and DNA, and a scanning confocal fluorescence microscope (SCFM) that can follow spFRET of two dye pairs on the same molecule. We will also develop a horizontal MT to follow tether length changes of the torsionally constrained DNA molecule induced by the immobilized helicase activity directly in the x- and y- plane as well as rotation of the DNA molecule in real time, and novel spFRET assays to understand the mechanism of action of a helicase. We will utilize the PcrA helicase in these studies. Helicases play critical roles in DNA and RNA metabolism, including DNA replication, repair, recombination and transcription. The genomes of Gram-positive bacteria encode an essential, conserved helicase, PcrA, which is involved in DNA repair and in plasmid rolling-circle replication, and also in as yet unidentified essential cellular processes. The experiments described in this proposal are likely to lead to the development of new instruments capable of combining the strengths of MT and spFRET, expand the ability of a SCFM to follow double spFRET, arid expand the use of MT to follow longitudinal and rotational movements generated by a motor protein on DNA. These instruments will allow studies on not only DNA helicases but also other motor proteins that act on nucleic acids, such as DNA and RNA polymerases, DNA repair and recombination factors, chromatin remodeling factors, etc. The experiments described here will also increase our understanding of the mechanism of action of an important group of motor proteins as exemplified by the PcrA helicase which is involved in a number of DNA transactions.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
3R01GM077872-04S1
Application #
7931210
Study Section
Special Emphasis Panel (ZRG1-BCMB-R (50))
Program Officer
Lewis, Catherine D
Project Start
2009-09-30
Project End
2011-04-30
Budget Start
2009-09-30
Budget End
2011-04-30
Support Year
4
Fiscal Year
2009
Total Cost
$227,250
Indirect Cost
Name
University of Pittsburgh
Department
Physiology
Type
Schools of Medicine
DUNS #
004514360
City
Pittsburgh
State
PA
Country
United States
Zip Code
15213
Rodriguez-Collazo, Pedro; Leuba, Sanford; Karahanian, Eduardo et al. (2014) Salt-urea, sulfopropyl-sepharose, and covalent chromatography methods for histone isolation and fractionation. Methods Mol Biol 1094:295-307
Fagerburg, Matt V; Schauer, Grant D; Thickman, Karen R et al. (2012) PcrA-mediated disruption of RecA nucleoprotein filaments--essential role of the ATPase activity of RecA. Nucleic Acids Res 40:8416-24
Lan, Li; Nakajima, Satoshi; Kapetanaki, Maria G et al. (2012) Monoubiquitinated histone H2A destabilizes photolesion-containing nucleosomes with concomitant release of UV-damaged DNA-binding protein E3 ligase. J Biol Chem 287:12036-49
Graham, Brian W; Schauer, Grant D; Leuba, Sanford H et al. (2011) Steric exclusion and wrapping of the excluded DNA strand occurs along discrete external binding paths during MCM helicase unwinding. Nucleic Acids Res 39:6585-95
Erb, Teresa M; Schneider, Corinne; Mucko, Sara E et al. (2011) Paracrine and epigenetic control of trophectoderm differentiation from human embryonic stem cells: the role of bone morphogenic protein 4 and histone deacetylases. Stem Cells Dev 20:1601-14
Fagerburg, Matt V; Leuba, Sanford H (2011) Optimal practices for surface-tethered single molecule total internal reflection fluorescence resonance energy transfer analysis. Methods Mol Biol 749:273-89
Fujimoto, Satoru; Tomschik, Miroslav; Zlatanova, Jordanka (2009) Does BLM helicase unwind nucleosomal DNA? Biochem Cell Biol 87:875-82
Leuba, Sanford H; Wheeler, Travis B; Cheng, Chao-Min et al. (2009) Structure and dynamics of single DNA molecules manipulated by magnetic tweezers and or flow. Methods 47:214-22
Rodriguez-Collazo, Pedro; Leuba, Sanford H; Zlatanova, Jordanka (2009) Robust methods for purification of histones from cultured mammalian cells with the preservation of their native modifications. Nucleic Acids Res 37:e81
Cheng, Chao-Min; Kim, Yongtae; Yang, Jui-Ming et al. (2009) Dynamics of individual polymers using microfluidic based microcurvilinear flow. Lab Chip 9:2339-47

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