echemi logo
Product
  • Product
  • Supplier
  • Inquiry
    Home > Active Ingredient News > Study of Nervous System > PNAS: Significant progress!

    PNAS: Significant progress!

    • Last Update: 2021-03-24
    • Source: Internet
    • Author: User
    Search more information of high quality chemicals, good prices and reliable suppliers, visit www.echemi.com

    News February 27, 2021/bioon.
    com" target="_blank">/---The protein tau helps stabilize the internal skeleton of neurons in the brain.
    In Alzheimer's disease (AD), toxic tau protein aggregates called tau oligomers promote disease progression and memory loss.
    In a new study, researchers from Boston University School of Medicine in the United States showed how these tau oligomers are formed and, accordingly, how to prevent them.
    The relevant research results were published online in the PNAS journal on February 22, 2021.
    The title of the paper is "TIA1 potentiates tau phase separation and promotes generation of toxic oligomeric tau".

    bioon.
    com" target="_blank">


    The RNA binding protein TIA1 replaces the crowding agent and allows the tau phase to separate.


    The picture is from PNAS, 2021, doi:10.



    This research is based on an emerging field in biology called "phase separation", which is based on the discovery that proteins form droplets, just like "oil in vinegar".
    The corresponding author of the paper, Dr.
    Benjamin Wolozin, Professor of Pharmacology and Experimental Therapeutics at Boston University School of Medicine, explained, “We found that droplets containing the RNA-binding protein TIA1 related to AD (and amyotrophic lateral sclerosis) form toxic tau.
    Oligomers provide the foundation.
    "

    Tau oligomers form droplets in TIA1 droplets and selectively form droplets with TIA1; other RNA binding proteins will not stimulate the formation of tau droplets or tau oligomers.
    "This study shows that mixing tau with TIA1 produces tau oligomers that are very lethal to neurons.
    These results answer the basic question of how tau becomes toxic.
    It also provides a powerful tool for screening Compounds capable of inhibiting the formation of toxic tau oligomers.
    "

    These researchers produced pure proteins in order to conduct experiments in solutions containing only the specific ingredients under study.
    Then they mixed these proteins together and tracked the formation of small droplets under a microscope.
    Surprisingly, they found that tau formed droplets in the larger TIA1 droplets, but not in the droplets of other proteins.
    They also measured the amount of toxic tau oligomers, and the results showed that the tau in the TIA1 droplets formed many toxic tau oligomers.

    According to Wolozin, tau and TIA1 appear together in pathology, and TIA1 is one of the few RNA binding proteins bioon.
    com/course_video/zhong-guo-ren-qun-ying-yang-he-yi-chuan-yin416058.
    html">genetically related to AD .
    He believes that this research can now be used to advance drug discovery in order to discover compounds that prevent the formation of tau oligomers.
    (Bioon.
    com)

    bioon.
    com/course_video/zhong-guo-ren-qun-ying-yang-he-yi-chuan-yin416058.
    html">Genetic

    Reference materials: Peter EA Ash et al.


    TIA1 potentiates tau phase separation and promotes generation of toxic oligomeric tau .
    PNAS, 2021,doi:10.


    Reference materials: Peter EA Ash et al.
    TIA1 potentiates tau phase separation and promotes generation of toxic oligomeric tau .
    PNAS, 2021,doi:10.
    1073/pnas.
    2014188118.
    Researchers identify biochemical process responsible for producing toxic tau
    https://medicalxpress.
    com /news/2021-02-biochemical-responsible-toxic-tau.
    html TIA1 potentiates tau phase separation and promotes generation of toxic oligomeric tau
    This article is an English version of an article which is originally in the Chinese language on echemi.com and is provided for information purposes only. This website makes no representation or warranty of any kind, either expressed or implied, as to the accuracy, completeness ownership or reliability of the article or any translations thereof. If you have any concerns or complaints relating to the article, please send an email, providing a detailed description of the concern or complaint, to service@echemi.com. A staff member will contact you within 5 working days. Once verified, infringing content will be removed immediately.

    Related Articles

    Contact Us

    The source of this page with content of products and services is from Internet, which doesn't represent ECHEMI's opinion. If you have any queries, please write to service@echemi.com. It will be replied within 5 days.

    Moreover, if you find any instances of plagiarism from the page, please send email to service@echemi.com with relevant evidence.