Scientists Discover Mechanism of Hearing in Near-Atomic Detail

2022-10-21

For the first time and in near-atomic detail, scientists at Oregon Health & Science University (OHSU) have revealed the structure of the key part of the inner ear responsible for hearing.

“This is the last sensory system in which that fundamental molecular machinery has remained unknown,” said senior author Eric Gouaux, Ph.D. He is a senior scientist with the OHSU Vollum Institute and a Howard Hughes Medical Institute investigator. “The molecular machinery that carries out this absolutely amazing process has been unresolved for decades.”

Until now.

Through years of meticulous research to isolate the process that enables the inner ear to convert vibrations into sound, known as the mechanosensory transduction complex, scientists were about to painstakingly piece together the structure.

Published on October 12 in the journal Nature, the study revealed the structure of the key part of the inner ear responsible for hearing through cryo-electron microscopy. This discovery could point the way toward developing fresh treatments for hearing impairments, which affect more than 460 million people worldwide.

“The auditory neuroscience field has been waiting for these results for decades, and now that they are right here — we are ecstatic.” — Peter Barr-Gillespie, Ph.D.

Revealed in the study is the detailed architecture of the inner ear complex that converts vibrations into electrical impulses that the brain translates as sound. Known as mechanosensory transduction, the process is responsible for the sensations of balance and sound.

To make the discovery, scientists exploited the fact that the roundworm Caenorhabditis elegans harbors a mechanosensory complex very similar to that of humans.

Resolving the basic structure is the first step, according to Gouaux.

“It immediately suggests mechanisms by which one might be able to compensate for those deficits,” Gouaux said. “If a mutation gives rise to a defect in the transduction channel that causes hearing loss, it’s possible to design a molecule that fits into that space and rescues the defect. Or it may mean we can strengthen interactions that have been weakened.”

Hearing loss can be inherited through gene mutations that alter the proteins comprising the mechanosensory transduction complex. Or it can occur from damage, including sustained exposure to loud noise. In either case, OHSU researchers’ discovery allows scientists to visualize the complex for the first time.

The finding is an extraordinary achievement, said one leading neuroscience researcher at OHSU who was not directly involved in the research.

“The auditory neuroscience field has been waiting for these results for decades, and now that they are right here — we are ecstatic,” said Peter Barr-Gillespie, Ph.D., an OHSU research scientist and national leader in hearing research. “The results from this paper immediately suggest new avenues of research, and so will invigorate the field for years to come.”

Barr-Gillespie also serves as the chief research officer and executive vice president at OHSU.

Researchers resolved the puzzle through careful cultivation and isolation techniques involving 60 million worms over almost five years.

“We spent several years optimizing worm-growth and protein-isolation methods, and had many ‘rock-bottom’ moments when we considered giving up,” co-first author Sarah Clark, Ph.D., a postdoctoral fellow in the Gouaux lab, wrote in a research brief published by Nature.

Sci Tech Daily, 21 October 2022
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