The long-term goal of our laboratory is to determine how a hair cell assembles and operate its mechanically sensitive hair bundle, and to determine how defects in genes responsible for bundle structure and function lead to deafness. In this project, we propose to finally accomplish biochemical purification of the hair cell?s transduction complex, the assembly of proteins?including the transduction channel itself?that mediates the mechanical-to-electrical transduction that is the key event in hearing and balance. In addition, as recent evidence has shown that Ca2+ entry through transduction channels fine-tunes stereocilia length and hence perfects the stereocilia staircase, we will purify the protein complexes that control stereocilia dimensions and determine whether they are regulated by transduction through Ca2+ entry. Finally, we will expand our computational model for tip-link regeneration to include stereocilia length regulation, with the goal of simulating the process of final adjustment of the stereocilia staircase. Predictions of this model will be tested in by examining tip links and stereocilia length in the chick cochlea, a robust experimental system for examining hair- bundle development. This project uses advanced biochemical purification techniques, including a new method for elution from immunoaffinity columns that allows sequential antibody purification steps without the use of harsh conditions. We also continue to pioneer the application of high sensitivity mass spectrometry methods for identifying and quantifying proteins in the inner ear. Even though the number of hair cells is limited in the inner ear and the molecules mediating transduction and stereocilia length regulation are scarce, these sensitive methods allow us to use a biochemical approach to investigate these processes. We expect that this project will determine the molecular composition of the transduction apparatus, including stoichiometry of the constituent proteins, and to define the steps in stereocilia dimension regulation that are controlled by Ca2+. Our computational model for transduction?s fine-tuning of stereocilia length should then set the stage for a future comprehensive model that can describe assembly of the hair bundle and its transduction apparatus.

Public Health Relevance

Public Health Relevance Hearing loss is a major health problem that significantly affects the life quality of affected individuals. Many forms of hearing loss arise from damage to hair cells, the cells that convert vibrations from sound or accelerations from head movements into electrical signals. We propose here to identify components of the machinery that regulates hair cell development and function, and show how those components interact to make the machinery mechanically sensitive.

Agency
National Institute of Health (NIH)
Institute
National Institute on Deafness and Other Communication Disorders (NIDCD)
Type
Research Project (R01)
Project #
5R01DC002368-26
Application #
9952113
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Freeman, Nancy
Project Start
1994-07-01
Project End
2023-06-30
Budget Start
2020-07-01
Budget End
2021-06-30
Support Year
26
Fiscal Year
2020
Total Cost
Indirect Cost
Name
Oregon Health and Science University
Department
Otolaryngology
Type
Schools of Medicine
DUNS #
096997515
City
Portland
State
OR
Country
United States
Zip Code
97239
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Krey, Jocelyn F; Drummond, Meghan; Foster, Sarah et al. (2016) Annexin A5 is the Most Abundant Membrane-Associated Protein in Stereocilia but is Dispensable for Hair-Bundle Development and Function. Sci Rep 6:27221
Geszvain, Kati; Smesrud, Logan; Tebo, Bradley M (2016) Identification of a Third Mn(II) Oxidase Enzyme in Pseudomonas putida GB-1. Appl Environ Microbiol 82:3774-3782

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