A breakthrough in understanding metabolite regulation of a central stress sensor - Calico Skip to content 0% Calico Research & Technology Research & Technology Publications Drug Development Drug Development Patients Partnering Leadership Careers Job Openings PostDoc Program Mission and Values Leadership Research & Technology Drug Development Patients Partnering Collaborator Profiles People Publications News & Media Press Releases Calico Stories Life at Calico Careers Job Openings PostDoc Program Contact Us Back to Stories Calico Stories A breakthrough in understanding metabolite regulation of a central stress sensor Understanding homeostasis in aging and disease could lead to the ability to target specific biological pathways involved in the pathology of disease. That’s why Calico scientists, led by Carmela Sidrauski, have been studying the integrated stress response (ISR) pathway since 2014, and specifically the protein complex eIF2B, which is inhibited when cells sense a variety of insults. By understanding how the stress sensor eIF2B is regulated in cells, it may be possible to develop modulators that attenuate the chronic expression of stress proteins that can lead to neurological conditions like Vanishing White Matter Disease (VWMD) or possibly ALS and restore the proteome to a functional state. Calico had breakthrough results when we brought our target — eIF2B — and associated expertise to a multiyear collaboration among various Calico labs, the University of Utah and biopharmaceutical partner AbbVie. Together, we uncovered that binding of sugar phosphates to eIF2B can activate it, suggesting a novel and direct link between nutrient status and the rate of protein synthesis in cells. Calico had already found that synthetic small molecules could activate the eIF2B complex and wondered if there were natural ligands in the cell that would also inhibit or activate it. Based on this hypothesis, the question was, are cellular metabolites directly modulating our target? Research revealed that eIF2B senses how much sugar a cell is getting and tells the cell to adjust the amount of protein it makes based on its energy status. “This is a significant, fundamental discovery, and it has definitely caught the attention of the academic community,” says Carmela. “This protein complex is ancestral, existing in yeasts, worms, mice and humans. Up to this point, we didn’t know that this is a way it’s regulated and it’s probably regulated like this in every species.” The implications of this discovery are still unfolding. Next is to explore the physiological relevance of metabolite regulation, which Calico will be doing along with others in the scientific community. Read the paper here. Join Our Team Join Our Team More stories November 23, 2021 Understanding cardiometabolic diseases using abdominal MRI scans Cardiometabolic diseases are an increasing global health burden. And Calico scientists, led by Madeleine Cule, are working with the University of Westminster and ... Keep Reading April 15, 2020 DCAF15: Understanding how natural killer cells may work The human immune system can recognize and kill cancer cells growing in the body by sensing mutated proteins on the surface of cancer ... Keep Reading See All Stories About Us Research & Technology Drug Development Leadership Partnering Our Story Life at Calico Resources Publications Calico Stories News & Media Patients Contact Us Contact Us Join Us Follow Us X LinkedIn Privacy Policy Notice at Collection Terms of Use Code of Conduct 2026 Calico Life Sciences LLC. All rights reserved. Close