Molecular characterization and gene disruption of mouse lysosomal putative serine carboxypeptidase 1

Kollmann K, Damme M, Deuschl F, Kahle J, D'Hooge R, Lüllmann-Rauch R, Lübke T (2009)
Febs Journal 276(5): 1356-1369.

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DOI
Autor*in
Kollmann, Katrin; Damme, MarkusUniBi; Deuschl, Florian; Kahle, Jörg; D'Hooge, Rudi; Lüllmann-Rauch, Renate; Lübke, TorbenUniBi
Einrichtung
Centrum für Biotechnologie > Institut für Biochemie und Biotechnik
Fakultät für Chemie > Biochemie I
Erscheinungsjahr
2009
Zeitschriftentitel
Febs Journal
Band
276
Ausgabe
5
Seite(n)
1356-1369
ISSN
1742-464X
Page URI
https://pub.uni-bielefeld.de/record/1940533

Zitieren

Kollmann K, Damme M, Deuschl F, et al. Molecular characterization and gene disruption of mouse lysosomal putative serine carboxypeptidase 1. Febs Journal. 2009;276(5):1356-1369.
Kollmann, K., Damme, M., Deuschl, F., Kahle, J., D'Hooge, R., Lüllmann-Rauch, R., & Lübke, T. (2009). Molecular characterization and gene disruption of mouse lysosomal putative serine carboxypeptidase 1. Febs Journal, 276(5), 1356-1369. https://doi.org/10.1111/j.1742-4658.2009.06877.x
Kollmann, Katrin, Damme, Markus, Deuschl, Florian, Kahle, Jörg, D'Hooge, Rudi, Lüllmann-Rauch, Renate, and Lübke, Torben. 2009. “Molecular characterization and gene disruption of mouse lysosomal putative serine carboxypeptidase 1”. Febs Journal 276 (5): 1356-1369.
Kollmann, K., Damme, M., Deuschl, F., Kahle, J., D'Hooge, R., Lüllmann-Rauch, R., and Lübke, T. (2009). Molecular characterization and gene disruption of mouse lysosomal putative serine carboxypeptidase 1. Febs Journal 276, 1356-1369.
Kollmann, K., et al., 2009. Molecular characterization and gene disruption of mouse lysosomal putative serine carboxypeptidase 1. Febs Journal, 276(5), p 1356-1369.
K. Kollmann, et al., “Molecular characterization and gene disruption of mouse lysosomal putative serine carboxypeptidase 1”, Febs Journal, vol. 276, 2009, pp. 1356-1369.
Kollmann, K., Damme, M., Deuschl, F., Kahle, J., D'Hooge, R., Lüllmann-Rauch, R., Lübke, T.: Molecular characterization and gene disruption of mouse lysosomal putative serine carboxypeptidase 1. Febs Journal. 276, 1356-1369 (2009).
Kollmann, Katrin, Damme, Markus, Deuschl, Florian, Kahle, Jörg, D'Hooge, Rudi, Lüllmann-Rauch, Renate, and Lübke, Torben. “Molecular characterization and gene disruption of mouse lysosomal putative serine carboxypeptidase 1”. Febs Journal 276.5 (2009): 1356-1369.

14 Zitationen in Europe PMC

Daten bereitgestellt von Europe PubMed Central.

Chemical Proteomic Analysis of Serine Hydrolase Activity in Niemann-Pick Type C Mouse Brain.
van Rooden EJ, van Esbroeck ACM, Baggelaar MP, Deng H, Florea BI, Marques ARA, Ottenhoff R, Boot RG, Overkleeft HS, Aerts JMFG, van der Stelt M., Front Neurosci 12(), 2018
PMID: 30018533
Mice, double deficient in lysosomal serine carboxypeptidases Scpep1 and Cathepsin A develop the hyperproliferative vesicular corneal dystrophy and hypertrophic skin thickenings.
Pan X, Wang Y, Lübke T, Hinek A, Pshezhetsky AV., PLoS One 12(2), 2017
PMID: 28234994
Serine carboxypeptidase SCPEP1 and Cathepsin A play complementary roles in regulation of vasoconstriction via inactivation of endothelin-1.
Pan X, Grigoryeva L, Seyrantepe V, Peng J, Kollmann K, Tremblay J, Lavoie JL, Hinek A, Lübke T, Pshezhetsky AV., PLoS Genet 10(2), 2014
PMID: 24586188
Molecular characterization of arylsulfatase G: expression, processing, glycosylation, transport, and activity.
Kowalewski B, Lübke T, Kollmann K, Braulke T, Reinheckel T, Dierks T, Damme M., J Biol Chem 289(40), 2014
PMID: 25135642
All-trans retinoic acid protects renal tubular epithelial cells against hypoxia induced injury in vitro.
Wan X, Li X, Bo H, Zhao Y, Liu L, Chen W, Yin Z, Cao C., Transplant Proc 45(2), 2013
PMID: 23267795
Arylsulfatase K, a novel lysosomal sulfatase.
Wiegmann EM, Westendorf E, Kalus I, Pringle TH, Lübke T, Dierks T., J Biol Chem 288(42), 2013
PMID: 23986440
Arylsulfatase G inactivation causes loss of heparan sulfate 3-O-sulfatase activity and mucopolysaccharidosis in mice.
Kowalewski B, Lamanna WC, Lawrence R, Damme M, Stroobants S, Padva M, Kalus I, Frese MA, Lübke T, Lüllmann-Rauch R, D'Hooge R, Esko JD, Dierks T., Proc Natl Acad Sci U S A 109(26), 2012
PMID: 22689975
The metabolic serine hydrolases and their functions in mammalian physiology and disease.
Long JZ, Cravatt BF., Chem Rev 111(10), 2011
PMID: 21696217
Chondrogenic effects of exogenous retinoic acid or a retinoic acid receptor antagonist (LE135) on equine chondrocytes and bone marrow-derived mesenchymal stem cells in monolayer culture.
Henderson SE, Santangelo KS, Bertone AL., Am J Vet Res 72(7), 2011
PMID: 21728848
Impaired lysosomal trimming of N-linked oligosaccharides leads to hyperglycosylation of native lysosomal proteins in mice with alpha-mannosidosis.
Damme M, Morelle W, Schmidt B, Andersson C, Fogh J, Michalski JC, Lübke T., Mol Cell Biol 30(1), 2010
PMID: 19884343
Vascular smooth muscle cell differentiation-2010.
Miano JM., J Biomed Res 24(3), 2010
PMID: 23554628
Serine carboxypeptidases in regulation of vasoconstriction and elastogenesis.
Pshezhetsky AV, Hinek A., Trends Cardiovasc Med 19(1), 2009
PMID: 19467448
Functional characterization of a putative serine carboxypeptidase in vascular smooth muscle cells.
Lee TH, Chen J, Miano JM., Circ Res 105(3), 2009
PMID: 19574551
NCU-G1 is a highly glycosylated integral membrane protein of the lysosome.
Schieweck O, Damme M, Schröder B, Hasilik A, Schmidt B, Lübke T., Biochem J 422(1), 2009
PMID: 19489740

44 References

Daten bereitgestellt von Europe PubMed Central.

The mannose 6-phosphate glycoprotein proteome.
Sleat DE, Della Valle MC, Zheng H, Moore DF, Lobel P., J. Proteome Res. 7(7), 2008
PMID: 18507433
Integral and associated lysosomal membrane proteins.
Schroder B, Wrocklage C, Pan C, Jager R, Kosters B, Schafer H, Elsasser HP, Mann M, Hasilik A., Traffic 8(12), 2007
PMID: 17897319
Proteomics of the lysosome
Lübke, Biochim Biophys Acta (), 2008
Synthesis of phosphorylated recognition marker in lysosomal enzymes is located in the cis part of Golgi apparatus.
Pohlmann R, Waheed A, Hasilik A, von Figura K., J. Biol. Chem. 257(10), 1982
PMID: 6279593
Mannose 6-phosphate receptors: new twists in the tale.
Ghosh P, Dahms NM, Kornfeld S., Nat. Rev. Mol. Cell Biol. 4(3), 2003
PMID: 12612639
The human brain mannose 6-phosphate glycoproteome: a complex mixture composed of multiple isoforms of many soluble lysosomal proteins.
Sleat DE, Lackland H, Wang Y, Sohar I, Xiao G, Li H, Lobel P., Proteomics 5(6), 2005
PMID: 15789345
Identification of novel lysosomal matrix proteins by proteome analysis.
Kollmann K, Mutenda KE, Balleininger M, Eckermann E, von Figura K, Schmidt B, Lubke T., Proteomics 5(15), 2005
PMID: 16145712
The human urine mannose 6-phosphate glycoproteome.
Sleat DE, Zheng H, Lobel P., Biochim. Biophys. Acta 1774(3), 2006
PMID: 17258946
The mannose 6-phosphate glycoprotein proteome.
Sleat DE, Della Valle MC, Zheng H, Moore DF, Lobel P., J. Proteome Res. 7(7), 2008
PMID: 18507433
Cloning of a novel retinoid-inducible serine carboxypeptidase from vascular smooth muscle cells.
Chen J, Streb JW, Maltby KM, Kitchen CM, Miano JM., J. Biol. Chem. 276(36), 2001
PMID: 11447226
Tissue expression of the novel serine carboxypeptidase Scpep1.
Lee TH, Streb JW, Georger MA, Miano JM., J. Histochem. Cytochem. 54(6), 2006
PMID: 16461364
Proton-relay system of carboxypeptidase Y as a sole catalytic site: studies on mutagenic replacement of his 397.
Jung G, Ueno H, Hayashi R., J. Biochem. 124(2), 1998
PMID: 9685740
Autocatalytic processing of recombinant human procathepsin B is a bimolecular process.
Rozman J, Stojan J, Kuhelj R, Turk V, Turk B., FEBS Lett. 459(3), 1999
PMID: 10526165
Lysosomal enzyme precursors in human fibroblasts. Activation of cathepsin D precursor in vitro and activity of beta-hexosaminidase A precursor towards ganglioside GM2.
Hasilik A, von Figura K, Conzelmann E, Nehrkorn H, Sandhoff K., Eur. J. Biochem. 125(2), 1982
PMID: 6214395
Proteolytic degradation of low density lipoproteins by arterial smooth muscle cells: the role of individual cathepsins.
Leake DS, Peters TJ., Biochim. Biophys. Acta 664(1), 1981
PMID: 7016193
Glycosylation of the Mr 46,000 mannose 6-phosphate receptor. Effect on ligand binding, stability, and conformation.
Wendland M, Waheed A, Schmidt B, Hille A, Nagel G, von Figura K, Pohlmann R., J. Biol. Chem. 266(7), 1991
PMID: 1847926
Mutation of the glycosylated asparagine residue 286 in human CLN2 protein results in loss of enzymatic activity.
Tsiakas K, Steinfeld R, Storch S, Ezaki J, Lukacs Z, Kominami E, Kohlschutter A, Ullrich K, Braulke T., Glycobiology 14(4), 2004
PMID: 14736728
Carboxypeptidases C and D.
Remington SJ, Breddam K., Meth. Enzymol. 244(), 1994
PMID: 7845212
Human lysosomal protective protein has cathepsin A-like activity distinct from its protective function.
Galjart NJ, Morreau H, Willemsen R, Gillemans N, Bonten EJ, d'Azzo A., J. Biol. Chem. 266(22), 1991
PMID: 1907282
Purification and properties of prolylcarboxypeptidase (angiotensinase C) from human kidney.
Odya CE, Marinkovic DV, Hammon KJ, Stewart TA, Erdos EG., J. Biol. Chem. 253(17), 1978
PMID: 28321
Cloning and characterization of CPVL, a novel serine carboxypeptidase, from human macrophages.
Mahoney JA, Ntolosi B, DaSilva RP, Gordon S, McKnight AJ., Genomics 72(3), 2001
PMID: 11401439
A vitellogenic-like carboxypeptidase expressed by human macrophages is localized in endoplasmic reticulum and membrane ruffles.
Harris J, Schwinn N, Mahoney JA, Lin HH, Shaw M, Howard CJ, da Silva RP, Gordon S., Int J Exp Pathol 87(1), 2006
PMID: 16436111
The A- and B-chains of carboxypeptidase I from germinated barley originate from a single precursor polypeptide.
Doan NP, Fincher GB., J. Biol. Chem. 263(23), 1988
PMID: 3403516
Expression of cDNA encoding the human "protective protein" associated with lysosomal beta-galactosidase and neuraminidase: homology to yeast proteases.
Galjart NJ, Gillemans N, Harris A, van der Horst GT, Verheijen FW, Galjaard H, d'Azzo A., Cell 54(6), 1988
PMID: 3136930
Molecular defect in combined beta-galactosidase and neuraminidase deficiency in man.
D'Azzo A, Hoogeveen A, Reuser AJ, Robinson D, Galjaard H., Proc. Natl. Acad. Sci. U.S.A. 79(15), 1982
PMID: 6812049
Carboxypeptidase Y: structural basis for protein sorting and catalytic triad.
Jung G, Ueno H, Hayashi R., J. Biochem. 126(1), 1999
PMID: 10393313
Expression, purification, and characterization of the yeast KEX1 gene product, a polypeptide precursor processing carboxypeptidase.
Latchinian-Sadek L, Thomas DY., J. Biol. Chem. 268(1), 1993
PMID: 8416959
Activity and deletion analysis of recombinant human cathepsin L expressed in Escherichia coli.
Smith SM, Gottesman MM., J. Biol. Chem. 264(34), 1989
PMID: 2684978
Identification of sites of mannose 6-phosphorylation on lysosomal proteins.
Sleat DE, Zheng H, Qian M, Lobel P., Mol. Cell Proteomics 5(4), 2006
PMID: 16399764
Multiple sulfatase deficiency is caused by mutations in the gene encoding the human C(alpha)-formylglycine generating enzyme.
Dierks T, Schmidt B, Borissenko LV, Peng J, Preusser A, Mariappan M, von Figura K., Cell 113(4), 2003
PMID: 12757705
The multiple sulfatase deficiency gene encodes an essential and limiting factor for the activity of sulfatases.
Cosma MP, Pepe S, Annunziata I, Newbold RF, Grompe M, Parenti G, Ballabio A., Cell 113(4), 2003
PMID: 12757706
Purified recombinant human prosaposin forms oligomers that bind procathepsin D and affect its autoactivation.
Gopalakrishnan MM, Grosch HW, Locatelli-Hoops S, Werth N, Smolenova E, Nettersheim M, Sandhoff K, Hasilik A., Biochem. J. 383(Pt. 3), 2004
PMID: 15255780
Enzymatic activity of lysosomal carboxypeptidase (cathepsin) A is required for proper elastic fiber formation and inactivation of endothelin-1.
Seyrantepe V, Hinek A, Peng J, Fedjaev M, Ernest S, Kadota Y, Canuel M, Itoh K, Morales CR, Lavoie J, Tremblay J, Pshezhetsky AV., Circulation 117(15), 2008
PMID: 18391110
Mouse model for the lysosomal disorder galactosialidosis and correction of the phenotype with overexpressing erythroid precursor cells.
Zhou XY, Morreau H, Rottier R, Davis D, Bonten E, Gillemans N, Wenger D, Grosveld FG, Doherty P, Suzuki K, Grosveld GC, d'Azzo A., Genes Dev. 9(21), 1995
PMID: 7590240
The two mannose 6-phosphate receptors transport distinct complements of lysosomal proteins.
Pohlmann R, Boeker MW, von Figura K., J. Biol. Chem. 270(45), 1995
PMID: 7592993
Molecular characterization of the hypothetical 66.3-kDa protein in mouse: lysosomal targeting, glycosylation, processing and tissue distribution.
Deuschl F, Kollmann K, von Figura K, Lubke T., FEBS Lett. 580(24), 2006
PMID: 17007843
Molecular characterization of the human Calpha-formylglycine-generating enzyme.
Preusser-Kunze A, Mariappan M, Schmidt B, Gande SL, Mutenda K, Wenzel D, von Figura K, Dierks T., J. Biol. Chem. 280(15), 2005
PMID: 15657036
[Effect of the injection of Triton WR 1339 on the hepatic lysosomes of the rat.]
WATTIAUX R, WIBO M, BAUDHUIN P., Arch. Int. Physiol. Biochim. 71(), 1963
PMID: 13999241
Biosynthesis and transport of cathepsin D in cultured human fibroblasts.
Gieselmann V, Pohlmann R, Hasilik A, Von Figura K., J. Cell Biol. 97(1), 1983
PMID: 6863385
Lysosomal peptidase measurement by sensitive fluorometric amino acid analysis.
Taylor S, Tappel AL., Anal. Biochem. 56(1), 1973
PMID: 4764684
A modified ninhydrin reagent for the photometric determination of amino acids and related compounds.
MOORE S, STEIN WH., J. Biol. Chem. 211(2), 1954
PMID: 13221596
An improved spectrophotometric assay for human plasma carboxypeptidase N1.
Plummer TH Jr, Kimmel MT., Anal. Biochem. 108(2), 1980
PMID: 7457880
Multivariate neurocognitive and emotional profile of a mannosidosis murine model for therapy assessment.
Caeyenberghs K, Balschun D, Roces DP, Schwake M, Saftig P, D'Hooge R., Neurobiol. Dis. 23(2), 2006
PMID: 16766199
Targeted disruption of the M(r) 46,000 mannose 6-phosphate receptor gene in mice results in misrouting of lysosomal proteins.
Koster A, Saftig P, Matzner U, von Figura K, Peters C, Pohlmann R., EMBO J. 12(13), 1993
PMID: 8262064
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