Hsp70 and the Unfolded Protein Response as a Challenging Drug Target and an Inspiration for Probe Molecule Development
Leila Terrab, Peter Wipf
Abstract
The unfolded protein response (UPR) is a cellular stress response mechanism that is critical for cell survival. Pharmacological modulation of the ATPase activity of the chaperone Hsp70 can trigger UPR-mediated cell death, thus removing pathogenic cells in human malignancies, or, alternatively, stimulate survival, thereby preventing apoptosis in neuronal cells and slowing the progress of inflammation, neurodegeneration, and aging. This Viewpoint highlights the complexity of the protein homeostasis network and discusses different approaches for modulating Hsp70 activity, including the use of a chemical reaction development-inspired library of Hsp70 agonists and antagonists.
Topics & Concepts
Unfolded protein responseNeurodegenerationHsp70Drug discoveryCell biologyChaperone (clinical)InflammationApoptosisProgrammed cell deathNeuroscienceDrug developmentSmall moleculeDrugHeat shock proteinBiologyEndoplasmic reticulumMedicineBioinformaticsPharmacologyImmunologyBiochemistryDiseaseGenePathologyHeat shock proteins researchComputational Drug Discovery MethodsProtein Structure and Dynamics