TY - CHAP
T1 - An Optimized Stress Granule Detection Method
T2 - Investigation of UBQLN2 Effect on Stress Granule Formation
AU - Alexander, Elizabeth J.
AU - Wang, Jiou
N1 - Publisher Copyright:
© 2023, Springer Science+Business Media, LLC, part of Springer Nature.
PY - 2023
Y1 - 2023
N2 - Stress granules (SGs) are cytosolic ribonucleoprotein granules that form via a liquid–liquid phase separation in response to environmental stresses such as heat, oxidative, and osmotic changes. Due to the condensation of low complexity, hydrophobic regions in core SG components in these highly dynamic granules, defects in SG maintenance and formation have been linked to toxic aggregate formation in neurodegenerative diseases such as amyotrophic lateral sclerosis and frontotemporal dementia. However, efforts to dissect mechanisms regulating SG formation and maintenance have been limited by methods of tracking protein–SG localization. Here we describe a method for detecting and quantifying recruitment of cytosolically enriched proteins to SGs by indirect immunofluorescence microscopy. Using this method, we tracked the transient recruitment of the cytosolically enriched ubiquitin-like protein, ubiquilin 2 (UBQLN2), and a number of other factors into SGs, demonstrating its utility (Alexander et al., Proc Natl Acad Sci U S A 115:E11485–E11494, 2018).
AB - Stress granules (SGs) are cytosolic ribonucleoprotein granules that form via a liquid–liquid phase separation in response to environmental stresses such as heat, oxidative, and osmotic changes. Due to the condensation of low complexity, hydrophobic regions in core SG components in these highly dynamic granules, defects in SG maintenance and formation have been linked to toxic aggregate formation in neurodegenerative diseases such as amyotrophic lateral sclerosis and frontotemporal dementia. However, efforts to dissect mechanisms regulating SG formation and maintenance have been limited by methods of tracking protein–SG localization. Here we describe a method for detecting and quantifying recruitment of cytosolically enriched proteins to SGs by indirect immunofluorescence microscopy. Using this method, we tracked the transient recruitment of the cytosolically enriched ubiquitin-like protein, ubiquilin 2 (UBQLN2), and a number of other factors into SGs, demonstrating its utility (Alexander et al., Proc Natl Acad Sci U S A 115:E11485–E11494, 2018).
KW - Colocalization analysis
KW - Immunofluorescence
KW - Simultaneous fixation and permeabilization
KW - Stress granule
KW - UBQLN2
KW - Ubiquilin
UR - https://www.scopus.com/pages/publications/85141005202
UR - https://www.scopus.com/pages/publications/85141005202#tab=citedBy
U2 - 10.1007/978-1-0716-2597-2_33
DO - 10.1007/978-1-0716-2597-2_33
M3 - Chapter
C2 - 36310224
AN - SCOPUS:85141005202
T3 - Methods in Molecular Biology
SP - 543
EP - 560
BT - Methods in Molecular Biology
PB - Humana Press Inc.
ER -