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Validation and assessment of preanalytical factors of a fluorometric in vitro assay for glucocerebrosidase activity in human cerebrospinal fluid
by
Maple-Grødem, Jodi
, Førland, Marthe Gurine Gunnarsdatter
, Oftedal, Linn
, Alves, Guido
, Lange, Johannes
in
631/1647/2196
/ 692/53
/ 692/617/375
/ alpha-Synuclein - deficiency
/ alpha-Synuclein - genetics
/ Cerebrospinal fluid
/ Dementia disorders
/ Enzymatic activity
/ Enzymes
/ Fluorometry - methods
/ Freeze-thawing
/ Glucosylceramidase
/ Glucosylceramidase - cerebrospinal fluid
/ Glucosylceramidase - genetics
/ Humanities and Social Sciences
/ Humans
/ In Vitro Techniques
/ Lewy bodies
/ Lewy Bodies - enzymology
/ Lewy Bodies - pathology
/ Lysosomes - genetics
/ Lysosomes - pathology
/ Movement disorders
/ multidisciplinary
/ Mutation - genetics
/ Neurodegenerative diseases
/ Parkinson Disease - cerebrospinal fluid
/ Parkinson Disease - diagnosis
/ Parkinson Disease - pathology
/ Parkinson's disease
/ Risk Factors
/ Science
/ Science (multidisciplinary)
2020
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Validation and assessment of preanalytical factors of a fluorometric in vitro assay for glucocerebrosidase activity in human cerebrospinal fluid
by
Maple-Grødem, Jodi
, Førland, Marthe Gurine Gunnarsdatter
, Oftedal, Linn
, Alves, Guido
, Lange, Johannes
in
631/1647/2196
/ 692/53
/ 692/617/375
/ alpha-Synuclein - deficiency
/ alpha-Synuclein - genetics
/ Cerebrospinal fluid
/ Dementia disorders
/ Enzymatic activity
/ Enzymes
/ Fluorometry - methods
/ Freeze-thawing
/ Glucosylceramidase
/ Glucosylceramidase - cerebrospinal fluid
/ Glucosylceramidase - genetics
/ Humanities and Social Sciences
/ Humans
/ In Vitro Techniques
/ Lewy bodies
/ Lewy Bodies - enzymology
/ Lewy Bodies - pathology
/ Lysosomes - genetics
/ Lysosomes - pathology
/ Movement disorders
/ multidisciplinary
/ Mutation - genetics
/ Neurodegenerative diseases
/ Parkinson Disease - cerebrospinal fluid
/ Parkinson Disease - diagnosis
/ Parkinson Disease - pathology
/ Parkinson's disease
/ Risk Factors
/ Science
/ Science (multidisciplinary)
2020
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Validation and assessment of preanalytical factors of a fluorometric in vitro assay for glucocerebrosidase activity in human cerebrospinal fluid
by
Maple-Grødem, Jodi
, Førland, Marthe Gurine Gunnarsdatter
, Oftedal, Linn
, Alves, Guido
, Lange, Johannes
in
631/1647/2196
/ 692/53
/ 692/617/375
/ alpha-Synuclein - deficiency
/ alpha-Synuclein - genetics
/ Cerebrospinal fluid
/ Dementia disorders
/ Enzymatic activity
/ Enzymes
/ Fluorometry - methods
/ Freeze-thawing
/ Glucosylceramidase
/ Glucosylceramidase - cerebrospinal fluid
/ Glucosylceramidase - genetics
/ Humanities and Social Sciences
/ Humans
/ In Vitro Techniques
/ Lewy bodies
/ Lewy Bodies - enzymology
/ Lewy Bodies - pathology
/ Lysosomes - genetics
/ Lysosomes - pathology
/ Movement disorders
/ multidisciplinary
/ Mutation - genetics
/ Neurodegenerative diseases
/ Parkinson Disease - cerebrospinal fluid
/ Parkinson Disease - diagnosis
/ Parkinson Disease - pathology
/ Parkinson's disease
/ Risk Factors
/ Science
/ Science (multidisciplinary)
2020
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Validation and assessment of preanalytical factors of a fluorometric in vitro assay for glucocerebrosidase activity in human cerebrospinal fluid
Journal Article
Validation and assessment of preanalytical factors of a fluorometric in vitro assay for glucocerebrosidase activity in human cerebrospinal fluid
2020
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Overview
Lysosomal dysfunction is an emerging feature in the pathology of Parkinson’s disease and Dementia with Lewy bodies. Mutations in the
GBA
gene, encoding the enzyme Glucocerebrosidase (GCase), have been identified as a genetic risk factor for these synucleinopathies. As a result, there has been a growing interest in the involvement of GCase in these diseases. This GCase activity assay is based on the catalytic hydrolysis of 4-methylumbelliferyl β-
d
-glucopyranoside that releases the highly fluorescent 4-methylumbelliferyl (4-MU). The final assay protocol was tested for the following parameters: Lower limit of quantification (LLOQ), precision, parallelism, linearity, spike recovery, number of freeze–thaw events, and sample handling stability. The GCase activity assay is within acceptable criteria for parallelism, precision and spike recovery. The LLOQ of this assay corresponds to an enzymatic activity of generating 0.26 pmol 4-MU/min/ml. The enzymatic activity was stable when samples were processed and frozen at − 80 °C within 4 h after the lumbar puncture procedure. Repetitive freeze–thaw events significantly decreased enzyme activity. We present the validation of an optimized in vitro GCase activity assay, based on commercially available components, to quantify its enzymatic activity in human cerebrospinal fluid and the assessment of preanalytical factors.
Publisher
Nature Publishing Group UK,Nature Publishing Group,Nature Portfolio
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