This subproject is one of many research subprojects utilizing theresources provided by a Center grant funded by NIH/NCRR. The subproject andinvestigator (PI) may have received primary funding from another NIH source,and thus could be represented in other CRISP entries. The institution listed isfor the Center, which is not necessarily the institution for the investigator.Many types of bacteria propel themselves through liquid media using whip-like structures known as flagella (www.ks.uiuc.edu/Research/flagellum/). The bacterial flagellum is a huge (several micrometers long, 20 nm wide), multiprotein assembly built of three domains: a basal body, acting as a motor; a hook, acting as a joint; and a filament, which makes up the bulk of the length of the flagellum and interacts with solvent to propel the bacterium. Depending on the direction of the torque applied by the basal body, the filament assumes different helical shapes. Under counter-clockwise rotation (as viewed from the exterior of the cell), several flagella form a single helical bundle which propels the cell along a straight line, referred to as running mode [1]. Under clockwise rotation, the individual flagella dissociate from the bundle and form separate right-handed helices, causing the cell to tumble. Varying the duration of running and tumbling, bacteria can move up or down a gradient of an attractant or repellent by a biased random walk. One of the unresolved questions about the flagellum is how the reversal of torque applied by the motor results in a switching between the helical shapes of the filament. This switching is a result of polymorphic transitions in the filament, when individual protein units slide against each other [2], but its molecular mechanism remains poorly understood despite extensive experimental work [3, 2, 4] and a recent computational study [5].

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Biotechnology Resource Grants (P41)
Project #
2P41RR005969-18
Application #
7601255
Study Section
Special Emphasis Panel (ZRG1-BCMB-E (40))
Project Start
2007-08-15
Project End
2008-07-31
Budget Start
2007-08-15
Budget End
2008-07-31
Support Year
18
Fiscal Year
2007
Total Cost
$41,269
Indirect Cost
Name
University of Illinois Urbana-Champaign
Department
Type
Organized Research Units
DUNS #
041544081
City
Champaign
State
IL
Country
United States
Zip Code
61820
Shim, Jiwook; Banerjee, Shouvik; Qiu, Hu et al. (2017) Detection of methylation on dsDNA using nanopores in a MoS2 membrane. Nanoscale 9:14836-14845
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Decker, Karl; Page, Martin; Aksimentiev, Aleksei (2017) Nanoscale Ion Pump Derived from a Biological Water Channel. J Phys Chem B 121:7899-7906
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Sun, Chang; Taguchi, Alexander T; Vermaas, Josh V et al. (2016) Q-Band Electron-Nuclear Double Resonance Reveals Out-of-Plane Hydrogen Bonds Stabilize an Anionic Ubisemiquinone in Cytochrome bo3 from Escherichia coli. Biochemistry 55:5714-5725
Belkin, Maxim; Aksimentiev, Aleksei (2016) Molecular Dynamics Simulation of DNA Capture and Transport in Heated Nanopores. ACS Appl Mater Interfaces 8:12599-608
Poudel, Kumud R; Dong, Yongming; Yu, Hang et al. (2016) A time course of orchestrated endophilin action in sensing, bending, and stabilizing curved membranes. Mol Biol Cell 27:2119-32
Vermaas, Josh V; Taguchi, Alexander T; Dikanov, Sergei A et al. (2015) Redox potential tuning through differential quinone binding in the photosynthetic reaction center of Rhodobacter sphaeroides. Biochemistry 54:2104-16
Belkin, Maxim; Chao, Shu-Han; Jonsson, Magnus P et al. (2015) Plasmonic Nanopores for Trapping, Controlling Displacement, and Sequencing of DNA. ACS Nano 9:10598-611
Shen, Rong; Han, Wei; Fiorin, Giacomo et al. (2015) Structural Refinement of Proteins by Restrained Molecular Dynamics Simulations with Non-interacting Molecular Fragments. PLoS Comput Biol 11:e1004368

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