Recent Microscopy Advances and the Applications to Huntington's Disease Research.

Fluorescence microscopy Huntingtin/HAP40 atomic force microscopy live cell imaging super-resolution microscopy tissue clearing

Journal

Journal of Huntington's disease
ISSN: 1879-6400
Titre abrégé: J Huntingtons Dis
Pays: Netherlands
ID NLM: 101589965

Informations de publication

Date de publication:
2022
Historique:
pubmed: 19 7 2022
medline: 9 9 2022
entrez: 18 7 2022
Statut: ppublish

Résumé

Huntingtin is a 3144 amino acid protein defined as a scaffold protein with many intracellular locations that suggest functions in these compartments. Expansion of the CAG DNA tract in the huntingtin first exon is the cause of Huntington's disease. An important tool in understanding the biological functions of huntingtin is molecular imaging at the single-cell level by microscopy and nanoscopy. The evolution of these technologies has accelerated since the Nobel Prize in Chemistry was awarded in 2014 for super-resolution nanoscopy. We are in a new era of light imaging at the single-cell level, not just for protein location, but also for protein conformation and biochemical function. Large-scale microscopy-based screening is also being accelerated by a coincident development of machine-based learning that offers a framework for truly unbiased data acquisition and analysis at very large scales. This review will summarize the newest technologies in light, electron, and atomic force microscopy in the context of unique challenges with huntingtin cell biology and biochemistry.

Identifiants

pubmed: 35848031
pii: JHD220536
doi: 10.3233/JHD-220536
pmc: PMC9484089
doi:

Substances chimiques

Huntingtin Protein 0
Nerve Tissue Proteins 0

Types de publication

Journal Article Review Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

269-280

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Auteurs

Mouhanad Babi (M)

McMaster Centre for Advanced Light Microscopy (CALM) McMaster University, Hamilton, Canada.

Kaitlyn Neuman (K)

Department of Biochemistry and Biomedical Sciences, McMaster University, Hamilton, Canada.

Christina Y Peng (CY)

Department of Biochemistry and Biomedical Sciences, McMaster University, Hamilton, Canada.

Tamara Maiuri (T)

Department of Biochemistry and Biomedical Sciences, McMaster University, Hamilton, Canada.

Celeste E Suart (CE)

Department of Biochemistry and Biomedical Sciences, McMaster University, Hamilton, Canada.

Ray Truant (R)

Department of Biochemistry and Biomedical Sciences, McMaster University, Hamilton, Canada.
McMaster Centre for Advanced Light Microscopy (CALM) McMaster University, Hamilton, Canada.

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Classifications MeSH