Small molecule modulation of a redox-sensitive stress granule protein dissolves stress granules with beneficial outcomes for familial amyotrophic lateral sclerosis models
Uechi H., Sridharan S., Nijssen J., Bilstein J., Iglesias-Artola J., Kishigami S., Casablancas-Antras V., Poser I., Martinez E., Boczek E., Wagner M., Tomschke N., de Jesus Domingues A., Pal A., Doeleman T., Kour S., Anderson EN., Stein F., Lee H., Zhang X., Fritsch A., Jahnel M., Fürsch J., Murthy A., Alberti S., Bickle M., Fawzi N., Nadler A., David D., Pandey U., Hermann A., Stengel F., Davis B., Baldwin A., Savitski M., Hyman A., Wheeler R.
Neurodegeneràve diseases such as amyotrophic lateral sclerosis (ALS) are oten associated with mutàons in proteins that are associated with stress granules. Stress granules are condensates formed by liquid-liquid phase separàon which, when aberrant, can lead to altered condensàon behaviours and disease phenotypes. Here, we identified lipoamide, a small molecule which specifically prevents cytoplasmic condensàon of stress granule proteins. Thermal proteome profiling showed that lipoamide preferentially stabilises intrinsically disordered domain-containing proteins. These include SRSF1 and SFPQ, stress granule proteins necessary for lipoamide activity. The redox state of SFPQ correlates with its condensate-dissolving behaviour, in concordance with the importance of the dithiolane ring for lipoamide activity. In animals, lipoamide ameliorates aging-associated aggregàon of a stress granule reporter, improves neuronal morphology, and recovers motor defects caused by expression of ALS-associated FUS and TDP-43 mutants. In conclusion, lipoamide is a well-tolerated small molecule modulator of stress granule condensàon and dissection of its molecular mechanism identified a cellular pathway for redox regulàon of stress granule formàon.