This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. Primary support for the subproject and the subproject's principal investigator may have been provided by other sources, including other NIH sources. The Total Cost listed for the subproject likely represents the estimated amount of Center infrastructure utilized by the subproject, not direct funding provided by the NCRR grant to the subproject or subproject staff. The Protein Production and Biophysical Characterization Core encompasses the production component in the name of the COBRE as well as aspects of characterization. Specifically, the Core covers membrane protein expression, extraction, purification and, if necessary, reconstitution, as well as sufficient characterization to ensure their suitability for more detailed structural and functional analysis. Some research on protein-detergent complexes and their interactions, leading to crystallization, is part of the biophysical characterization effort as well. The Core provides instrumentation as well as scientific support, with a new element being a facility to assist investigators in developing and optimizing expression systems for proteins. A particular component of the characterization effort is devoted to scattering methods, of which it is especially X-ray and neutron scattering that represent distinctive and powerful capabilities that can shed considerable light on membrane proteins in solution. The COBRE is collaborating on neutron scattering methods with the Center for Neutron Science at the University of Delaware, which operates under a cooperative agreement with the National Center for Neutron Science.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Center Core Grants (P30)
Project #
5P30RR031160-02
Application #
8364942
Study Section
Special Emphasis Panel (ZRR1-RI-2 (01))
Project Start
2011-09-01
Project End
2012-08-31
Budget Start
2011-09-01
Budget End
2012-08-31
Support Year
2
Fiscal Year
2011
Total Cost
$294,094
Indirect Cost
Name
University of Delaware
Department
Engineering (All Types)
Type
Schools of Engineering
DUNS #
059007500
City
Newark
State
DE
Country
United States
Zip Code
19716
Naranjo, Andrea N; McNeely, Patrick M; Katsaras, John et al. (2016) Impact of purification conditions and history on A2A adenosine receptor activity: The role of CHAPS and lipids. Protein Expr Purif 124:62-7
Choi, Yong Seok; Lee, Kelvin H (2016) Multiple reaction monitoring assay based on conventional liquid chromatography and electrospray ionization for simultaneous monitoring of multiple cerebrospinal fluid biomarker candidates for Alzheimer's disease. Arch Pharm Res 39:390-7
Modla, Shannon; Caplan, Jeffrey L; Czymmek, Kirk J et al. (2015) Localization of fluorescently tagged protein to plasmodesmata by correlative light and electron microscopy. Methods Mol Biol 1217:121-33
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Cui, Weier; Wang, Xu; Lee, Jung-Youn (2015) Drop-ANd-See: a simple, real-time, and noninvasive technique for assaying plasmodesmal permeability. Methods Mol Biol 1217:149-56
Min, Lie; Choe, Leila H; Lee, Kelvin H (2015) Improved protease digestion conditions for membrane protein detection. Electrophoresis 36:1690-8
Naranjo, Andrea N; Chevalier, Amy; Cousins, Gregory D et al. (2015) Conserved disulfide bond is not essential for the adenosine A2A receptor: Extracellular cysteines influence receptor distribution within the cell and ligand-binding recognition. Biochim Biophys Acta 1848:603-14
Guo, Changmiao; Hou, Guangjin; Lu, Xingyu et al. (2014) Fast magic angle spinning NMR with heteronucleus detection for resonance assignments and structural characterization of fully protonated proteins. J Biomol NMR 60:219-29
Suiter, Christopher L; Paramasivam, Sivakumar; Hou, Guangjin et al. (2014) Sensitivity gains, linearity, and spectral reproducibility in nonuniformly sampled multidimensional MAS NMR spectra of high dynamic range. J Biomol NMR 59:57-73
Lee, Jung-Youn (2014) New and old roles of plasmodesmata in immunity and parallels to tunneling nanotubes. Plant Sci 221-222:13-20

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