Literature DB >> 29339442

Specific Substrate for the Assay of Lysosomal Acid Lipase.

Sophia Masi1, Naveen Chennamaneni1, Frantisek Turecek1, C Ronald Scott2, Michael H Gelb3.   

Abstract

BACKGROUND: Deficiency of lysosomal acid lipase (LAL) causes Wolman disease and cholesterol ester storage disease. With the recent introduction of enzyme replacement therapy to manage LAL deficiency comes the need for a reliable assay of LAL enzymatic activity that can be applied to dried blood spots (DBS).
METHODS: We prepared and tested a library of analogs of palmitoyl 4-methylumbelifferyl esters to find a highly active and specific substrate for LAL in DBS. The LAL assay was optimized leading to both LC-MS/MS and fluorometric assay of LAL. We tested the new assay on DBS from healthy and LAL-deficient patients.
RESULTS: The ester formed between palmitic acid and 4-propyl-8-methyl-7-hydroxycoumarin (P-PMHC) was found to be >98% selective for LAL in DBS based on the sensitivity of its activity to the LAL-specific inactivator Lalistat-2 and the fact that the activity was close to zero using DBS from patients previously shown to be LAL-deficient. Use of P-PMHC and heavy isotope-labeled internal standard with optimized assay conditions led to an approximately 2-fold increase in the specific activity of LAL compared with the previously reported LAL assay. Patients deficient in LAL were readily distinguished from normal persons with the new LAL assay using UPLC-MS/MS or fluorometric assay platforms.
CONCLUSIONS: The new assay can measure LAL in DBS with a single measurement compared with the previous method involving 2 assays done in parallel.
© 2017 American Association for Clinical Chemistry.

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Year:  2018        PMID: 29339442      PMCID: PMC6383652          DOI: 10.1373/clinchem.2017.282251

Source DB:  PubMed          Journal:  Clin Chem        ISSN: 0009-9147            Impact factor:   8.327


  11 in total

1.  Direct multiplex assay of lysosomal enzymes in dried blood spots for newborn screening.

Authors:  Yijun Li; C Ronald Scott; Nestor A Chamoles; Ahmad Ghavami; B Mario Pinto; Frantisek Turecek; Michael H Gelb
Journal:  Clin Chem       Date:  2004-08-03       Impact factor: 8.327

2.  Tandem mass spectrometry for the direct assay of lysosomal enzymes in dried blood spots: application to screening newborns for mucopolysaccharidosis II (Hunter Syndrome).

Authors:  Brian J Wolfe; Sophie Blanchard; Martin Sadilek; C Ronald Scott; Frantisek Turecek; Michael H Gelb
Journal:  Anal Chem       Date:  2010-12-30       Impact factor: 6.986

3.  Expression and functional characterization of human lysosomal acid lipase gene (LIPA) mutation responsible for cholesteryl ester storage disease (CESD) phenotype.

Authors:  Francis Rajamohan; Allan R Reyes; Wanida Ruangsiriluk; Lise R Hoth; Seungil Han; Nicole Caspers; Meihua Tu; Jessica Ward; Ravi G Kurumbail
Journal:  Protein Expr Purif       Date:  2015-01-22       Impact factor: 1.650

Review 4.  Gastric lipase: crystal structure and activity.

Authors:  S Canaan; A Roussel; R Verger; C Cambillau
Journal:  Biochim Biophys Acta       Date:  1999-11-23

5.  A new method for the measurement of lysosomal acid lipase in dried blood spots using the inhibitor Lalistat 2.

Authors:  John Hamilton; Iain Jones; Rajeev Srivastava; Peter Galloway
Journal:  Clin Chim Acta       Date:  2012-03-29       Impact factor: 3.786

6.  New spectrophotometric assays of acid lipase and their use in the diagnosis of Wolman and cholesteryl ester storage diseases.

Authors:  A Nègre; R Salvayre; A Dagan; C Borrone; S Gatt
Journal:  Anal Biochem       Date:  1985-03       Impact factor: 3.365

7.  Tandem Mass Spectrometry Has a Larger Analytical Range than Fluorescence Assays of Lysosomal Enzymes: Application to Newborn Screening and Diagnosis of Mucopolysaccharidoses Types II, IVA, and VI.

Authors:  Arun Babu Kumar; Sophia Masi; Farideh Ghomashchi; Naveen Kumar Chennamaneni; Makoto Ito; C Ronald Scott; Frantisek Turecek; Michael H Gelb; Zdenek Spacil
Journal:  Clin Chem       Date:  2015-09-14       Impact factor: 8.327

8.  Survival in infants treated with sebelipase Alfa for lysosomal acid lipase deficiency: an open-label, multicenter, dose-escalation study.

Authors:  Simon A Jones; Sandra Rojas-Caro; Anthony G Quinn; Mark Friedman; Sachin Marulkar; Fatih Ezgu; Osama Zaki; J Jay Gargus; Joanne Hughes; Dominique Plantaz; Roshni Vara; Stephen Eckert; Jean-Baptiste Arnoux; Anais Brassier; Kim-Hanh Le Quan Sang; Vassili Valayannopoulos
Journal:  Orphanet J Rare Dis       Date:  2017-02-08       Impact factor: 4.123

9.  Pilot study of newborn screening for six lysosomal storage diseases using Tandem Mass Spectrometry.

Authors:  Susan Elliott; Norman Buroker; Jason J Cournoyer; Anna M Potier; Joseph D Trometer; Carole Elbin; Mack J Schermer; Jaana Kantola; Aaron Boyce; Frantisek Turecek; Michael H Gelb; C Ronald Scott
Journal:  Mol Genet Metab       Date:  2016-05-20       Impact factor: 4.797

Review 10.  Targeting Wolman Disease and Cholesteryl Ester Storage Disease: Disease Pathogenesis and Therapeutic Development.

Authors:  Francis Aguisanda; Natasha Thorne; Wei Zheng
Journal:  Curr Chem Genom Transl Med       Date:  2017-01-30
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2.  Quantification of 11 enzyme activities of lysosomal storage disorders using liquid chromatography-tandem mass spectrometry.

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Journal:  Mol Genet Metab Rep       Date:  2018-09-07

3.  A kinetic assay of total lipase activity for detecting lysosomal acid lipase deficiency (LAL-D) and the molecular characterization of 18 LAL-D patients from Russia.

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Journal:  JIMD Rep       Date:  2019-06-03

4.  Early diagnosis of infantile-onset lysosomal acid lipase deficiency in the advent of available enzyme replacement therapy.

Authors:  Jennifer L Cohen; Jessica Burfield; Karen Valdez-Gonzalez; Angela Samuels; Arianna K Stefanatos; Marc Yudkoff; Helio Pedro; Can Ficicioglu
Journal:  Orphanet J Rare Dis       Date:  2019-08-14       Impact factor: 4.123

5.  Sebelipase alfa enzyme replacement therapy in Wolman disease: a nationwide cohort with up to ten years of follow-up.

Authors:  Tanguy Demaret; Florence Lacaille; Camille Wicker; Jean-Baptiste Arnoux; Juliette Bouchereau; Claire Belloche; Cyril Gitiaux; David Grevent; Christine Broissand; Dalila Adjaoud; Marie-Thérèse Abi Warde; Dominique Plantaz; Soumeya Bekri; Pascale de Lonlay; Anaïs Brassier
Journal:  Orphanet J Rare Dis       Date:  2021-12-14       Impact factor: 4.123

6.  LC-MS/MS-based enzyme assay for lysosomal acid lipase using dried blood spots.

Authors:  Mari Ohira; Marianne Barr; Torayuki Okuyama; Ryuichi Mashima
Journal:  Mol Genet Metab Rep       Date:  2022-08-26

7.  A Case of Lysosomal Acid Lipase Deficiency Confirmed by Response to Sebelipase Alfa Therapy.

Authors:  Joseph J Shen; Jessica L Davis; Xinying Hong; Fred H Laningham; Michael H Gelb; Grace E Kim
Journal:  J Pediatr Gastroenterol Nutr       Date:  2020-12       Impact factor: 3.288

Review 8.  Biomarkers for Lysosomal Storage Disorders with an Emphasis on Mass Spectrometry.

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Journal:  Int J Mol Sci       Date:  2020-04-14       Impact factor: 5.923

  8 in total

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