Combatting Proteostasis Imbalance in Age-Related Neurodegenerative Disorders: Targeted Modulation of Molecular Chaperone Networks

Authors

  • Avery Parker PhD
  • Henry Wood Professor
  • Cameron Phillips Associate Professor

Keywords:

Proteostasis, Neurodegeneration, Molecular Chaperones, CRISPR-Cas9, Protein Misfolding, Alzheimer's Disease, Parkinson's Disease

Abstract

Proteostasis imbalance is a hallmark of age-related neurodegenerative diseases. This study investigates the modulation of molecular chaperone networks to restore proteostasis in cellular models of Alzheimer's and Parkinson's diseases. Using cutting-edge CRISPR-Cas9 gene editing and proteomics, we identified key chaperones capable of ameliorating protein misfolding. The results demonstrate that targeted chaperone modulation can significantly reduce proteotoxic stress, offering insights into therapeutic strategies for neurodegeneration.

Author Biographies

Avery Parker, PhD

PhD
Harvard University
Cambridge, MA 02138, USA

Henry Wood, Professor

Professor
Oxford University
Oxford OX1 2JD, United Kingdom

Cameron Phillips, Associate Professor

Associate Professor
University of Toronto
Toronto, ON M5S, Canada

References

Kumar, R. V., Sharma, V. K., Chattopadhyay, B., & Chakraborty, S. (2012). An improved plant regeneration and Agrobacterium-mediated transformation of red pepper (Capsicum annuum L.). Physiology and Molecular Biology of Plants, 18(4), 357-364.

Sharma, V., Zheng, W., Huang, J., & Cook, D. E. (2020). CRISPR-Cas RNA targeting using transient Cas13a expression in Nicotiana benthamiana. In RNA Abundance Analysis: Methods and Protocols (pp. 1-18). New York, NY: Springer US.

Published

2024-12-24

Issue

Section

Articles