Literature DB >> 15789345

The human brain mannose 6-phosphate glycoproteome: a complex mixture composed of multiple isoforms of many soluble lysosomal proteins.

David E Sleat1, Henry Lackland, Yanhong Wang, Istvan Sohar, Gang Xiao, Hong Li, Peter Lobel.   

Abstract

The lysosome is a membrane delimited cytoplasmic organelle that contains at least 50 hydrolytic enzymes and associated cofactors. The biomedical importance of these enzymes is highlighted by the many lysosomal storage disorders that are associated with mutations in genes encoding lysosomal proteins, and there is also evidence that lysosomal activities may be involved in more widespread human diseases. The aim of this study was to characterize the human brain lysosomal proteome with the goal of establishing a reference map to investigate human diseases of unknown etiology and to gain insights into the cellular function of the lysosome. Proteins containing mannose 6-phosphate (Man6-P), a carbohydrate modification used for targeting resident soluble lysosomal proteins to the lysosome, were affinity-purified using immobilized Man6-P receptor. Fractionation by two-dimensional electrophoresis resolved a complex mixture comprising approximately 800 spots. Constituent proteins in each spot were identified using a combination of matrix-assisted laser desorption/ionization-time of flight mass spectrometry (both peptide mass fingerprinting and tandem mass spectrometry) [corrected] on in-gel tryptic digests and N-terminal sequencing. In a complementary analysis, we also analyzed a tryptic digest of the unfractionated mixture by liquid chromatography MS/MS. In total, 61 different proteins were identified. Seven were likely contaminants associated with true Man6-P glycoproteins. Forty-one were known lysosomal proteins of which 11 have not previously been reported to contain Man6-P. An additional nine proteins were either uncharacterized or proteins not previously reported to have lysosomal function. We found that the human brain Man6-P-containing lysosomal proteome is highly complex and contains more proteins with a much greater number of individual isoforms than found in previous studies of Man6-P glycoproteomes.

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Year:  2005        PMID: 15789345     DOI: 10.1002/pmic.200401054

Source DB:  PubMed          Journal:  Proteomics        ISSN: 1615-9853            Impact factor:   3.984


  37 in total

1.  Intracellular localization of p40, a protein identified in a preparation of lysosomal membranes.

Authors:  Marielle Boonen; Isabelle Hamer; Muriel Boussac; Anne-Françoise Delsaute; Bruno Flamion; Jérôme Garin; Michel Jadot
Journal:  Biochem J       Date:  2006-04-01       Impact factor: 3.857

2.  Degradation of fibrillar forms of Alzheimer's amyloid beta-peptide by macrophages.

Authors:  Amitabha Majumdar; Haeyong Chung; Georgia Dolios; Rong Wang; Nikiya Asamoah; Peter Lobel; Frederick R Maxfield
Journal:  Neurobiol Aging       Date:  2007-01-11       Impact factor: 4.673

Review 3.  Proteomics of the peroxisome.

Authors:  R A Saleem; J J Smith; J D Aitchison
Journal:  Biochim Biophys Acta       Date:  2006-09-12

4.  Purification, characterization, gene cloning, and expression of a novel alcohol dehydrogenase with anti-prelog stereospecificity from Candida parapsilosis.

Authors:  Yao Nie; Yan Xu; Xiao Qing Mu; Hai Yan Wang; Ming Yang; Rong Xiao
Journal:  Appl Environ Microbiol       Date:  2007-04-13       Impact factor: 4.792

5.  The human urine mannose 6-phosphate glycoproteome.

Authors:  David E Sleat; Haiyan Zheng; Peter Lobel
Journal:  Biochim Biophys Acta       Date:  2006-12-20

6.  Neuropeptide changes and neuroactive amino acids in CSF from humans and sheep with neuronal ceroid lipofuscinoses (NCLs, Batten disease).

Authors:  Graham W Kay; Marcel M Verbeek; Julie M Furlong; Michèl A A P Willemsen; David N Palmer
Journal:  Neurochem Int       Date:  2009-08-05       Impact factor: 3.921

Review 7.  Lysosome biogenesis and lysosomal membrane proteins: trafficking meets function.

Authors:  Paul Saftig; Judith Klumperman
Journal:  Nat Rev Mol Cell Biol       Date:  2009-08-12       Impact factor: 94.444

8.  A new large animal model of CLN5 neuronal ceroid lipofuscinosis in Borderdale sheep is caused by a nucleotide substitution at a consensus splice site (c.571+1G>A) leading to excision of exon 3.

Authors:  Tony Frugier; Nadia L Mitchell; Imke Tammen; Peter J Houweling; Donald G Arthur; Graham W Kay; Otto P van Diggelen; Robert D Jolly; David N Palmer
Journal:  Neurobiol Dis       Date:  2007-09-29       Impact factor: 5.996

9.  Rapid inactivation of proteins by rapamycin-induced rerouting to mitochondria.

Authors:  Margaret S Robinson; Daniela A Sahlender; Samuel D Foster
Journal:  Dev Cell       Date:  2010-02-16       Impact factor: 12.270

10.  Novel interactions of CLN5 support molecular networking between Neuronal Ceroid Lipofuscinosis proteins.

Authors:  Annina Lyly; Carina von Schantz; Claudia Heine; Mia-Lisa Schmiedt; Tessa Sipilä; Anu Jalanko; Aija Kyttälä
Journal:  BMC Cell Biol       Date:  2009-11-26
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