Real-Time Detection of Glutamate using Templated Polymers as Shape-Changing Target Receptors

Information

  • Research Project
  • 10195790
  • ApplicationId
    10195790
  • Core Project Number
    R21EB031433
  • Full Project Number
    1R21EB031433-01
  • Serial Number
    031433
  • FOA Number
    PAR-20-084
  • Sub Project Id
  • Project Start Date
    4/1/2021 - 3 years ago
  • Project End Date
    12/31/2023 - 5 months ago
  • Program Officer Name
    ATANASIJEVIC, TATJANA
  • Budget Start Date
    4/1/2021 - 3 years ago
  • Budget End Date
    12/31/2021 - 2 years ago
  • Fiscal Year
    2021
  • Support Year
    01
  • Suffix
  • Award Notice Date
    3/18/2021 - 3 years ago

Real-Time Detection of Glutamate using Templated Polymers as Shape-Changing Target Receptors

PROJECT SUMMARY / ABSTRACT There is a great demand for a new sensing technology that can monitor neurochemicals in brain continuously in real-time with high temporal resolution. While electrochemical detection of electroactive neurotransmitters (such as dopamine and serotonin) have been successful using high frequency voltammetric methods (such as fast- scan cyclic voltammetry), measurement of non-electroactive species (such as glutamate) still remain a great challenge for achieving real-time monitoring with high time resolution. The goal of this project is to implement a new electrochemical sensing platform that can monitor glutamate, a well-known non-electroactive neurotransmitter, with physiologically relevant detection range and high temporal resolution. The proposed sensing approach can serve as an alternative to enzymatic sensing or microdialysis which have some limitations with respect to time resolution and stability. Motivated in part by the aptamer-based electrochemical sensors, the proposed sensing mechanism utilizes a novel synthetic target receptor as both a target recognition unit and a signal transducer. The glutamate receptor is formed by a single-chain stimuli-responsive templated polymer that binds specifically to its template molecule, namely, glutamate. Furthermore, upon selective target recognition, the polymer undergoes conformation change (from linear to folded shape). This change in polymer morphology can be electrochemically detected through the use of a redox reporter (such as ferrocene) attached to the polymer. For validation of the proposed sensing approach, the developed sensor will be compared against two well-established methods, a patch clamp and a microdialysis technique. A patch clamp system is ideal for measuring fast dynamics (milliseconds) of chemical exchange at the synaptic cleft of the neurons, however, lacks chemical specificity. A microdialysis in conjunction with liquid chromatography and mass spectrometry provides exceptional chemical specificity, however, the temporal resolution is poor (on the order of minutes). It is expected that the developed sensor platform will be able to bridge the gap between these two existing methods and to provide versatility in sensing performances. The goals of this project will be achieved by pursuing the following specific aims: (1) optimization of the templated polymer-based glutamate receptor to meet the desired performance metrics; and (2) validation of the developed glutamate sensor in a physiological environment. The successful outcome of this project will be the development of a new general platform technology for detection of neurochemicals in real-time with a time resolution that is sufficient for studying synaptic communications as well as for monitoring chemicals in the extracellular regions in the brain tissue.

IC Name
NATIONAL INSTITUTE OF BIOMEDICAL IMAGING AND BIOENGINEERING
  • Activity
    R21
  • Administering IC
    EB
  • Application Type
    1
  • Direct Cost Amount
    125000
  • Indirect Cost Amount
    54571
  • Total Cost
    179571
  • Sub Project Total Cost
  • ARRA Funded
    False
  • CFDA Code
    286
  • Ed Inst. Type
    BIOMED ENGR/COL ENGR/ENGR STA
  • Funding ICs
    NIBIB:179571\
  • Funding Mechanism
    Non-SBIR/STTR RPGs
  • Study Section
    BNVT
  • Study Section Name
    Bioengineering of Neuroscience, Vision and Low Vision Technologies Study Section
  • Organization Name
    UNIVERSITY OF NEW HAMPSHIRE
  • Organization Department
    ENGINEERING (ALL TYPES)
  • Organization DUNS
    111089470
  • Organization City
    DURHAM
  • Organization State
    NH
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    038242620
  • Organization District
    UNITED STATES