Proteomics of the lysosome

Lübke T, Lobel P, Sleat DE (2009)
Biochimica et Biophysica Acta 1793(4): 625-635.

No fulltext has been uploaded. References only!
Journal Article | Review | Published | English

No fulltext has been uploaded

; ;
Publishing Year

Cite this

Lübke T, Lobel P, Sleat DE. Proteomics of the lysosome. Biochimica et Biophysica Acta. 2009;1793(4):625-635.
Lübke, T., Lobel, P., & Sleat, D. E. (2009). Proteomics of the lysosome. Biochimica et Biophysica Acta, 1793(4), 625-635. doi:10.1016/j.bbamcr.2008.09.018
Lübke, T., Lobel, P., and Sleat, D. E. (2009). Proteomics of the lysosome. Biochimica et Biophysica Acta 1793, 625-635.
Lübke, T., Lobel, P., & Sleat, D.E., 2009. Proteomics of the lysosome. Biochimica et Biophysica Acta, 1793(4), p 625-635.
T. Lübke, P. Lobel, and D.E. Sleat, “Proteomics of the lysosome”, Biochimica et Biophysica Acta, vol. 1793, 2009, pp. 625-635.
Lübke, T., Lobel, P., Sleat, D.E.: Proteomics of the lysosome. Biochimica et Biophysica Acta. 1793, 625-635 (2009).
Lübke, Torben, Lobel, Peter, and Sleat, David E. “Proteomics of the lysosome”. Biochimica et Biophysica Acta 1793.4 (2009): 625-635.
This data publication is cited in the following publications:
This publication cites the following data publications:

89 Citations in Europe PMC

Data provided by Europe PubMed Central.

Lysosomal degradation of membrane lipids.
Kolter T, Sandhoff K., FEBS Lett 584(9), 2010
PMID: 19836391
Functions of the alpha, beta, and gamma subunits of UDP-GlcNAc:lysosomal enzyme N-acetylglucosamine-1-phosphotransferase.
Qian Y, Lee I, Lee WS, Qian M, Kudo M, Canfield WM, Lobel P, Kornfeld S., J Biol Chem 285(5), 2010
PMID: 19955174
Differential time course of FSH/FSH receptor complex endocytosis within sertoli and germ cells during rat testis development.
Segretain D, Gilleron J, Carette D, Denizot JP, Pointis G., Dev Dyn 239(4), 2010
PMID: 20201104
Pathophysiology of neuropathic lysosomal storage disorders.
Bellettato CM, Scarpa M., J Inherit Metab Dis 33(4), 2010
PMID: 20429032
Comparative proteomic analysis of plasma membrane proteins between human osteosarcoma and normal osteoblastic cell lines.
Zhang Z, Zhang L, Hua Y, Jia X, Li J, Hu S, Peng X, Yang P, Sun M, Ma F, Cai Z., BMC Cancer 10(), 2010
PMID: 20470422
Structural basis for recognition of phosphodiester-containing lysosomal enzymes by the cation-independent mannose 6-phosphate receptor.
Olson LJ, Peterson FC, Castonguay A, Bohnsack RN, Kudo M, Gotschall RR, Canfield WM, Volkman BF, Dahms NM., Proc Natl Acad Sci U S A 107(28), 2010
PMID: 20615935
The proteome of lysosomes.
Schröder BA, Wrocklage C, Hasilik A, Saftig P., Proteomics 10(22), 2010
PMID: 20957757
Mass spectrometry-based protein profiling to determine the cause of lysosomal storage diseases of unknown etiology.
Sleat DE, Ding L, Wang S, Zhao C, Wang Y, Xin W, Zheng H, Moore DF, Sims KB, Lobel P., Mol Cell Proteomics 8(7), 2009
PMID: 19383612
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
Lysosome biogenesis and lysosomal membrane proteins: trafficking meets function.
Saftig P, Klumperman J., Nat Rev Mol Cell Biol 10(9), 2009
PMID: 19672277

99 References

Data provided by Europe PubMed Central.

MERP1: a mammalian ependymin-related protein gene differentially expressed in hematopoietic cells.
Gregorio-King CC, McLeod JL, Collier FM, Collier GR, Bolton KA, Van Der Meer GJ, Apostolopoulos J, Kirkland MA., Gene 286(2), 2002
PMID: 11943480
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
Carboxypeptidase Y: structural basis for protein sorting and catalytic triad.
Jung G, Ueno H, Hayashi R., J. Biochem. 126(1), 1999
PMID: 10393313
Tissue expression of the novel serine carboxypeptidase Scpep1.
Lee TH, Streb JW, Georger MA, Miano JM., J. Histochem. Cytochem. 54(6), 2006
PMID: 16461364
Purification and properties of major alpha-D-mannosidase in the luminal fluid of porcine epididymis.
Jin YZ, Dacheux F, Dacheux JL, Bannai S, Sugita Y, Okamura N., Biochim. Biophys. Acta 1432(2), 1999
PMID: 10407159
Refinement of the expression pattern of a mouse homologue of the porcine 135-kDa alpha-d-mannosidase (MAN2B2).
Tascou S, Nayernia K, Engel W, Burfeind P., Biochem. Biophys. Res. Commun. 272(3), 2000
PMID: 10860856
Characterization of a human core-specific lysosomal {alpha}1,6-mannosidase involved in N-glycan catabolism.
Park C, Meng L, Stanton LH, Collins RE, Mast SW, Yi X, Strachan H, Moremen KW., J. Biol. Chem. 280(44), 2005
PMID: 16115860
A human lysosomal alpha(1----6)-mannosidase active on the branched trimannosyl core of complex glycans.
Daniel PF, Evans JE, De Gasperi R, Winchester B, Warren CD., Glycobiology 2(4), 1992
PMID: 1421754
A human lysosomal alpha-mannosidase specific for the core of complex glycans.
De Gasperi R, Daniel PF, Warren CD., J. Biol. Chem. 267(14), 1992
PMID: 1577805
The core-specific lysosomal alpha(1-6)-mannosidase activity depends on aspartamidohydrolase activity.
Haeuw JF, Grard T, Alonso C, Strecker G, Michalski JC., Biochem. J. 297 ( Pt 3)(), 1994
PMID: 8110182
Characterization of RNASET2, the first human member of the Rh/T2/S family of glycoproteins.
Campomenosi P, Salis S, Lindqvist C, Mariani D, Nordstrom T, Acquati F, Taramelli R., Arch. Biochem. Biophys. 449(1-2), 2006
PMID: 16620762
Identification of acyloxyacyl hydrolase, a lipopolysaccharide-detoxifying enzyme, in the murine urinary tract.
Feulner JA, Lu M, Shelton JM, Zhang M, Richardson JA, Munford RS., Infect. Immun. 72(6), 2004
PMID: 15155618
Intracellular localization of p40, a protein identified in a preparation of lysosomal membranes.
Boonen M, Hamer I, Boussac M, Delsaute AF, Flamion B, Garin J, Jadot M., Biochem. J. 395(1), 2006
PMID: 16367739
TMEM74, a lysosome and autophagosome protein, regulates autophagy.
Yu C, Wang L, Lv B, Lu Y, Zeng L, Chen Y, Ma D, Shi T, Wang L., Biochem. Biophys. Res. Commun. 369(2), 2008
PMID: 18294959
Sanfilippo syndrome type C: deficiency of acetyl-CoA:alpha-glucosaminide N-acetyltransferase in skin fibroblasts.
Klein U, Kresse H, von Figura K., Proc. Natl. Acad. Sci. U.S.A. 75(10), 1978
PMID: 33384
Mutations in TMEM76* cause mucopolysaccharidosis IIIC (Sanfilippo C syndrome).
Hrebicek M, Mrazova L, Seyrantepe V, Durand S, Roslin NM, Noskova L, Hartmannova H, Ivanek R, Cizkova A, Poupetova H, Sikora J, Urinovska J, Stranecky V, Zeman J, Lepage P, Roquis D, Verner A, Ausseil J, Beesley CE, Maire I, Poorthuis BJ, van de Kamp J, van Diggelen OP, Wevers RA, Hudson TJ, Fujiwara TM, Majewski J, Morgan K, Kmoch S, Pshezhetsky AV., Am. J. Hum. Genet. 79(5), 2006
PMID: 17033958
Mutational analysis of the HGSNAT gene in Italian patients with mucopolysaccharidosis IIIC (Sanfilippo C syndrome). Mutation in brief #959. Online.
Fedele AO, Filocamo M, Di Rocco M, Sersale G, Lubke T, di Natale P, Cosma MP, Ballabio A., Hum. Mutat. 28(5), 2007
PMID: 17397050
The novel neuronal ceroid lipofuscinosis gene MFSD8 encodes a putative lysosomal transporter.
Siintola E, Topcu M, Aula N, Lohi H, Minassian BA, Paterson AD, Liu XQ, Wilson C, Lahtinen U, Anttonen AK, Lehesjoki AE., Am. J. Hum. Genet. 81(1), 2007
PMID: 17564970


0 Marked Publications

Open Data PUB

Web of Science

View record in Web of Science®


PMID: 18977398
PubMed | Europe PMC

Search this title in

Google Scholar