Screening methods for identifying pharmacological chaperones

Min Hyeon Shin, Hyun Suk Lim

Research output: Contribution to journalReview article

11 Scopus citations

Abstract

Protein folding is crucial for most proteins to achieve their correct three-dimensional conformations and function properly. Defects in protein folding frequently caused by mutations lead to a range of protein misfolding diseases, including Alzheimer's disease, Parkinson's disease, cystic fibrosis, amyloidosis, Gaucher disease, etc. One approach to treat these devastating diseases would be to use pharmacological chaperones, which are small-molecules that bind to and stabilize misfolded proteins, thereby correcting their pathogenic misfolding and rescuing their functions. As such, pharmacological chaperone therapy holds great promise for the treatment of numerous protein misfolding diseases. In this review, we highlight recent strategies for identifying small-molecules that act as pharmacological chaperones and revert protein misfolding diseases, with a focus on reports within the last five years.

Original languageEnglish (US)
Pages (from-to)638-647
Number of pages10
JournalMolecular BioSystems
Volume13
Issue number4
DOIs
StatePublished - Jan 1 2017
Externally publishedYes

ASJC Scopus subject areas

  • Biotechnology
  • Molecular Biology

Fingerprint Dive into the research topics of 'Screening methods for identifying pharmacological chaperones'. Together they form a unique fingerprint.

  • Cite this