Analysis of lysosomal hydrolase trafficking and activity in human iPSC-derived neuronal models

Summary: Lysosomes are critical for maintaining protein homeostasis and cellular metabolism. Lysosomal dysfunction and disrupted protein trafficking contribute to cell death in neurodegenerative disorders, including Parkinson's disease and dementia. We describe three complementary protocols—the...

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Main Authors: Leah K. Cuddy, Joseph R. Mazzulli
Format: Article
Language:English
Published: Elsevier 2021-03-01
Series:STAR Protocols
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2666166721000472
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spelling doaj-972f185adfbb4c6c81836d8c77165e642021-03-22T12:53:19ZengElsevierSTAR Protocols2666-16672021-03-0121100340Analysis of lysosomal hydrolase trafficking and activity in human iPSC-derived neuronal modelsLeah K. Cuddy0Joseph R. Mazzulli1The Ken and Ruth Davee Department of Neurology, Northwestern University Feinberg School of Medicine, Chicago, IL 60611, USA; Corresponding authorThe Ken and Ruth Davee Department of Neurology, Northwestern University Feinberg School of Medicine, Chicago, IL 60611, USA; Corresponding authorSummary: Lysosomes are critical for maintaining protein homeostasis and cellular metabolism. Lysosomal dysfunction and disrupted protein trafficking contribute to cell death in neurodegenerative disorders, including Parkinson's disease and dementia. We describe three complementary protocols—the use of protein glycosylation, western blotting, immunofluorescence, and hydrolase activity measurement—to analyze the trafficking and activity of lysosomal proteins in patient-derived neurons differentiated from iPSCs. These methods should help to identify lysosomal phenotypes in patient-derived cultures and aid the discovery of therapeutics that augment lysosomal function.For complete details on the use and execution of this protocol, please refer to Cuddy et al. (2019).http://www.sciencedirect.com/science/article/pii/S2666166721000472NeuroscienceProtein biochemistryStem cells
collection DOAJ
language English
format Article
sources DOAJ
author Leah K. Cuddy
Joseph R. Mazzulli
spellingShingle Leah K. Cuddy
Joseph R. Mazzulli
Analysis of lysosomal hydrolase trafficking and activity in human iPSC-derived neuronal models
STAR Protocols
Neuroscience
Protein biochemistry
Stem cells
author_facet Leah K. Cuddy
Joseph R. Mazzulli
author_sort Leah K. Cuddy
title Analysis of lysosomal hydrolase trafficking and activity in human iPSC-derived neuronal models
title_short Analysis of lysosomal hydrolase trafficking and activity in human iPSC-derived neuronal models
title_full Analysis of lysosomal hydrolase trafficking and activity in human iPSC-derived neuronal models
title_fullStr Analysis of lysosomal hydrolase trafficking and activity in human iPSC-derived neuronal models
title_full_unstemmed Analysis of lysosomal hydrolase trafficking and activity in human iPSC-derived neuronal models
title_sort analysis of lysosomal hydrolase trafficking and activity in human ipsc-derived neuronal models
publisher Elsevier
series STAR Protocols
issn 2666-1667
publishDate 2021-03-01
description Summary: Lysosomes are critical for maintaining protein homeostasis and cellular metabolism. Lysosomal dysfunction and disrupted protein trafficking contribute to cell death in neurodegenerative disorders, including Parkinson's disease and dementia. We describe three complementary protocols—the use of protein glycosylation, western blotting, immunofluorescence, and hydrolase activity measurement—to analyze the trafficking and activity of lysosomal proteins in patient-derived neurons differentiated from iPSCs. These methods should help to identify lysosomal phenotypes in patient-derived cultures and aid the discovery of therapeutics that augment lysosomal function.For complete details on the use and execution of this protocol, please refer to Cuddy et al. (2019).
topic Neuroscience
Protein biochemistry
Stem cells
url http://www.sciencedirect.com/science/article/pii/S2666166721000472
work_keys_str_mv AT leahkcuddy analysisoflysosomalhydrolasetraffickingandactivityinhumanipscderivedneuronalmodels
AT josephrmazzulli analysisoflysosomalhydrolasetraffickingandactivityinhumanipscderivedneuronalmodels
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