TY - JOUR
T1 - Superresolution fluorescence imaging of mutant huntingtin aggregation in cells
AU - Vonk, Willianne
AU - Sahl, Steffen J.
PY - 2019
Y1 - 2019
N2 - Fluorescence-based nanoscopy methods (also known as "superresolution" microscopy) have substantially expanded our options to examine the distributions of molecules inside cells with nanometer-scale resolution and molecular specificity. In the biophysical analysis of aggregation-prone misfolded proteins and peptides, this has enabled the visualization of distinct populations of aggregated species such as fibrillar assemblies within intact neuronal cells, well below previous limits of sensitivity and resolution. With the Huntington's disease protein, polyglutamine-expanded mutant huntingtin, as an example, we provide sample preparation and imaging protocols for superresolution microscopy down to the ~30 nm-level.
AB - Fluorescence-based nanoscopy methods (also known as "superresolution" microscopy) have substantially expanded our options to examine the distributions of molecules inside cells with nanometer-scale resolution and molecular specificity. In the biophysical analysis of aggregation-prone misfolded proteins and peptides, this has enabled the visualization of distinct populations of aggregated species such as fibrillar assemblies within intact neuronal cells, well below previous limits of sensitivity and resolution. With the Huntington's disease protein, polyglutamine-expanded mutant huntingtin, as an example, we provide sample preparation and imaging protocols for superresolution microscopy down to the ~30 nm-level.
KW - amyloid
KW - cellular superresolution imaging
KW - fibrillar aggregates
KW - fibrils
KW - fluorescence nanoscopy
KW - Huntington's disease
KW - inclusion bodies
KW - oligomers
KW - polyglutamine expansion
KW - trinucleotide repeat disorders
M3 - Article
SN - 1064-3745
VL - 1873
SP - 241
JO - Methods in molecular biology (Clifton, N.J.)
JF - Methods in molecular biology (Clifton, N.J.)
M1 - doi: 10.1007/978-1-4939-8820-4_15
ER -