• More insight into how vision works

    From ScienceDaily@1:317/3 to All on Mon Jan 3 21:30:38 2022
    More insight into how vision works

    Date:
    January 3, 2022
    Source:
    Paul Scherrer Institute
    Summary:
    Scientists have shed light on an important component of the eye:
    a protein in the rod cells of the retina which helps us see in
    dim light.

    Acting as an ion channel in the cell membrane, the protein is
    responsible for relaying the optical signal from the eye to the
    brain. If a genetic disorder disrupts the molecular function in
    a person, they will go blind.

    Scientists have deciphered the protein's three-dimensional
    structure, preparing the way for innovative medical treatments.



    FULL STORY ==========================================================================
    PSI scientists have shed light on an important component of the eye:
    a protein in the rod cells of the retina which helps us see in dim
    light. Acting as an ion channel in the cell membrane, the protein is responsible for relaying the optical signal from the eye to the brain. If
    a genetic disorder disrupts the molecular function in a person, they will
    go blind. Scientists have deciphered the protein's three-dimensional
    structure, preparing the way for innovative medical treatments. The
    study is published in the scientific journal Nature Structural &
    Molecular Biology.


    ========================================================================== "It's thanks to the rod cells in our eye that we can observe the stars in
    the night sky," explains Jacopo Marino, a biologist with PSI's Laboratory
    of Biomolecular Research. "These photo cells are so sensitive to light
    that they can detect even a single photon reaching us from a very remote
    part of the universe -- a truly incredible feat." The ability of our
    brain to eventually translate these light beams into a visual impression
    is partly down to the cyclic nucleotide-gated (CNG) ion channels whose three-dimensional structure has now been illuminated by a PSI research
    group led by Jacopo Marino.

    The ion channel acts as a gatekeeper controlling whether specific
    particles are allowed through to the interior of the receptor cell. It
    is embedded in the protein-rich shell -- the cell membrane -- of the
    rod cells. In darkness, the ion channel, and thus the gate to the cell,
    is completely open. But when light hits the eye, it triggers a cascade
    of processes in the rod cells. This ultimately causes the gate to close,
    with the result that positively charged particles, such as calcium ions,
    can no longer enter into the cell.

    This electrochemical signal continues via the nerve cells into the
    brain's visual cortex, where a visual impression -- such as a flash of
    light -- is created. "The idea of solving the structure of this channel
    dates back to nearly 20 years ago, when Gebhard Schertler and Benjamin
    Kaupp already collaborated on this topic," says Jacopo Marino. Both are co-authors of the new study.

    Endurance paid off PhD student Diane Barret first had to extract the
    channel protein from cows' eyes supplied by an abattoir -- a complicated
    and arduous process. "This was a very challenging task, as the protein
    is extremely sensitive and decomposes very quickly. In addition, it
    is only available in tiny quantities in the source material," Barret
    explains. It took a whole two years to obtain enough protein to work
    with. "We were both too stubborn to simply give up," says Jacopo Marino, laughing. "But in the end that stubbornness paid off." The scientists
    then used cryo-electron microscopy to reveal the three- dimensional
    structure of the ion channel. "In contrast to previous studies on the
    structure of the ion channel, we investigated the native protein as it
    exists in the eye. We are therefore much closer to the real conditions
    that exist in living creatures," Diane Barret says.

    One of the reasons why a clearer understanding of the channel protein's
    natural structure is important is to advance the development of treatments
    for genetic disorders for which there is no known cure, such as retinitis pigmentosa. With this disease, photoreceptors gradually die off, leaving
    people blind. One possible cause is that the body is unable to correctly produce the CNG channel protein due to a genetic defect. As a result, the
    ion channel does not close completely when light hits the eye, disrupting
    the cell's electrochemical balance and causing the cells to die.

    "If we could find molecules that affect the protein in such a way that
    the channel would completely close, we could prevent the cells from dying
    -- and thus stop people going blind," explains Jacopo Marino. Now that researchers have identified the precise structure of the protein they
    are able to search specifically for such molecules.

    Additional barrier The protein comprises four parts: three lots of subunit
    A, and one lot of subunit B. A correctly functioning ion channel is
    only possible in this combination. In their study, PSI scientists show
    why the B subunit seems to play such an important role: a side arm of
    the protein -- a single amino acid - - protrudes from the rest of the
    protein, like a barrier across a gateway. This narrows the passage in
    the channel to the point where no ions can pass through.

    "No one expected that -- it came as a total surprise," says Diane
    Barret. Other narrow places already exist in the A subunit -- like
    main gateways -- which were previously thought to be the only ones. It
    is interesting to note that the additional barrier is found not only
    in the protein from the cow's eye, but seems to apply to all types of
    animal, as the scientists showed. Whether crocodiles, eagles or humans
    -- all living creatures with an ion channel in their eye have the same protruding amino acid at this position in the protein.

    As it has been preserved so consistently during evolution, it must be
    essential for the functioning of the channel.

    special promotion Explore the latest scientific research on sleep and
    dreams in this free online course from New Scientist -- Sign_up_now_>>> academy.newscientist.com/courses/science-of-sleep-and-dreams ========================================================================== Story Source: Materials provided by Paul_Scherrer_Institute. Original
    written by Brigitte Osterath. Note: Content may be edited for style
    and length.


    ========================================================================== Journal Reference:
    1. Diane C. A. Barret, Gebhard F. X. Schertler, U. Benjamin Kaupp,
    Jacopo
    Marino. The structure of the native CNGA1/CNGB1 CNG channel from
    bovine retinal rods. Nature Structural & Molecular Biology, 2021;
    DOI: 10.1038/ s41594-021-00700-8 ==========================================================================

    Link to news story: https://www.sciencedaily.com/releases/2022/01/220103121742.htm
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