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New Tools

BAG1-BAG6

New Tools for Proteostasis Research

We (the Proteostasis Consortium) are pleased to share the development of new tools for the community.  These tools are designed for your open access here on the Proteostasis Consortium Website.  We invite you to participate in our community effort by sharing your insights. 

Human Proteostasis Network Annotation

Human Proteostasis Network Annotation

Human Proteostasis Network Annotation

The human proteostasis network has been annotation gene-by-gene by members of the Proteostasis Consortium.  Chapter 1. Components of Translation, Protein Folding, and Organelle-Specific Systems will be available on the website and on bioRxiv. Shortly thereafter, we will post and submit to bioRxiv Chapter 2. Components of the Ubiquitin-Proteasome System, Chapter 3. Components of the Autophagy Lysosomal Pathway and Chapter 4. Analysis of Expression Patterns of the Human Proteostasis Network in Aging and Neurodegenerative Diseases.

Proteostasis Pharmacology Subgroup

P3 PR Table Aug 2022

Proteostasis Pharmacology Subgroup

The Proteostasis Pharmacology Subgroup of the Proteostasis Consortium was formed to coordinate the discovery, characterization and use of small molecule modulators of the Proteostasis Network. Our goals are to (i) develop new chemical probes for high value targets in the Proteostasis Network, (ii) share current information about the best validated chemical probes with members of the Proteostasis Consortium and beyond (iii) build and maintain a collection of best-in-class chemical probes for a range of targets in the Proteostasis Network. The long term goal of our subgroup is to identify ways of using small molecules to delay or reverse age-dependent neurodegenerative diseases.

Towards these goals, the Proteostasis Pharmacology Subgroup is currently developing two resources (see New Tools tab). The first resource is an annotated list of small molecules that have undergone rigorous evaluation as chemical probes. The second is to an up-to-date list of publicly available small molecules that perturb targets in the Protoestasis Network. This validated collection, once established and fully characterized, will be made available to the proteostasis research community at-large.

Finally, research programs being conducted within the Proteostasis Consortium and our collaborators are building new tools for targeting the major degradation pathways (e.g., autophagy and the proteasome). As these tools advance, they will also be shared with the wider research community.

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