The broad, long-term objective of the PI is to achieve ultrasensitivity in amperometric biosensing. This project is the first step toward this direction.
The specific aims of this project are: 1. To assemble protein/enzyme molecules directly on the bare surface of nanoscale spatially confined regions on electrodes to reduce denaturation of the molecules and to form nanoscale (from 1 mu m to 100 nm) assemblies, 2. To demonstrate reduced protein denaturation and enhanced (several orders of magnitude) electron transfer across the molecule-electrode interface of the nanoscale assemblies. To accomplish specific aim 1, SPM-based fabrication techniques will be used to generate nanoscale templates on the surface of semiconductor and metallic electrodes. The templates will contain nanoscale spatially confined regions. Protein/enzyrnes molecules will be immobilized using different mechanisms into these regions to make physical contact with the bare surface of the electrodes. In-situ SPM imaging with submolecular resolution will be used to characterize the immobilized molecules in relation to preservation of their native conformation.To accomplish specific aim 2, electrochemical characterization of the nanoscale assemblies will be carried out to measure the current flowing across the molecule-electrode interface. Electrochemical characterization will indicate the enhancement of current level and the degree of reduction of denaturation. Electrochemical characterization will be performed using the ultrahigh sensitivity of a potentiostat that has current resolution on the femtoampere level. More precise characterization of electron transfer across regions of the interface will be made using in-situ scanning tunneling spectroscopy. This highly localized tunneling will be used to probe the interaction between electrons and the active centers of protein/enzyme molecules, allowing a fundamental study of electron transfer rate and hence the limiting factor for electron transfer. This project investigates an essential requirement for achieving ultrasensifivity in amperometric biosensing. Amperometric biosensors with significantly improved sensitivity are demanded in clinical and environmental applications, including detecting extremely small amounts of adrenaline in treatment of tumors, monitoring pesticides, and the realization of in-vivo and implantable subcutaneous sensors. Also, nanoscale sensing schemes provides additional improvement of sensitivity and allows measurement of small amount of samples. It is expected that the results of this project will be used as a general approach for obtaining enhanced electron transfer rate via immobilized proteins.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Minority Biomedical Research Support - MBRS (S06)
Project #
5S06GM060654-08
Application #
7391708
Study Section
Minority Programs Review Committee (MPRC)
Project Start
Project End
Budget Start
2007-04-01
Budget End
2008-03-31
Support Year
8
Fiscal Year
2007
Total Cost
$186,196
Indirect Cost
Name
Hunter College
Department
Type
DUNS #
620127915
City
New York
State
NY
Country
United States
Zip Code
10065
Luine, Victoria; Gomez, Juan; Beck, Kevin et al. (2017) Sex differences in chronic stress effects on cognition in rodents. Pharmacol Biochem Behav 152:13-19
Gupta, Rupal; Huang, Wenlin; Francesconi, Lynn C et al. (2017) Effect of positional isomerism and vanadium substitution on 51V magic angle spinning NMR Spectra Of Wells-Dawson polyoxotungstates. Solid State Nucl Magn Reson 84:28-33
Luine, Victoria (2016) Estradiol: Mediator of memories, spine density and cognitive resilience to stress in female rodents. J Steroid Biochem Mol Biol 160:189-95
Frankfurt, Maya; Luine, Victoria (2015) The evolving role of dendritic spines and memory: Interaction(s) with estradiol. Horm Behav 74:28-36
Luine, Victoria (2015) Recognition memory tasks in neuroendocrine research. Behav Brain Res 285:158-64
DeCicco, Jennifer M; O'Toole, Laura J; Dennis, Tracy A (2014) The late positive potential as a neural signature for cognitive reappraisal in children. Dev Neuropsychol 39:497-515
Luine, Victoria N (2014) Estradiol and cognitive function: past, present and future. Horm Behav 66:602-18
Garcia, Miguel; Ray, Sibnath; Brown, Isaiah et al. (2014) PakD, a putative p21-activated protein kinase in Dictyostelium discoideum, regulates actin. Eukaryot Cell 13:119-26
O'Toole, Laura J; DeCicco, Jennifer M; Berthod, Samantha et al. (2013) The N170 to angry faces predicts anxiety in typically developing children over a two-year period. Dev Neuropsychol 38:352-63
Garcia, Rebecca; Nguyen, Liem; Brazill, Derrick (2013) Dictyostelium discoideum SecG interprets cAMP-mediated chemotactic signals to influence actin organization. Cytoskeleton (Hoboken) 70:269-80

Showing the most recent 10 out of 202 publications