Mannose 6 Dephosphorylation of Lysosomal Proteins Mediated by Acid Phosphatases Acp2 and Acp5
- Georgia Makrypidia,
- Markus Dammeb,
- Sven Müller-Loenniesc,
- Maria Truschd,
- Bernhard Schmidtb,
- Hartmut Schlüterd,
- Joerg Heerene,
- Torben Lübkef,
- Paul Saftigg and
- Thomas Braulkea
- aDepartment of Biochemistry, Children's Hospital, University Medical Center Hamburg-Eppendorf, Hamburg, Germany
- bDepartment of Biochemistry 2, Georg-August University Göttingen, Göttingen, Germany
- cResearch Center Borstel, Leibniz Center for Medicine and Biosciences, Borstel, Germany
- dDepartment of Clinical Chemistry, University Medical Center Hamburg-Eppendorf, Hamburg, Germany
- eDepartment of Biochemistry and Molecular Cell Biology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany
- fInstitute of Biochemistry I, University of Bielefeld, Bielefeld, Germany
- gInstitute of Biochemistry, Christian-Albrechts-Universität Kiel, Kiel, Germany
ABSTRACT
Mannose 6-phosphate (Man6P) residues represent a recognition signal required for efficient receptor-dependent transport of soluble lysosomal proteins to lysosomes. Upon arrival, the proteins are rapidly dephosphorylated. We used mice deficient for the lysosomal acid phosphatase Acp2 or Acp5 or lacking both phosphatases (Acp2/Acp5−/−) to examine their role in dephosphorylation of Man6P-containing proteins. Two-dimensional (2D) Man6P immunoblot analyses of tyloxapol-purified lysosomal fractions revealed an important role of Acp5 acting in concert with Acp2 for complete dephosphorylation of lysosomal proteins. The most abundant lysosomal substrates of Acp2 and Acp5 were identified by Man6P affinity chromatography and mass spectrometry. Depending on the presence of Acp2 or Acp5, the isoelectric point of the lysosomal cholesterol-binding protein Npc2 ranged between 7.0 and 5.4 and may thus regulate its interaction with negatively charged lysosomal membranes at acidic pH. Correspondingly, unesterified cholesterol was found to accumulate in lysosomes of cultured hepatocytes of Acp2/Acp5−/− mice. The data demonstrate that dephosphorylation of Man6P-containing lysosomal proteins requires the concerted action of Acp2 and Acp5 and is needed for hydrolysis and removal of degradation products.
FOOTNOTES
- Received 29 August 2011.
- Returned for modification 27 September 2011.
- Accepted 2 December 2011.
- Address correspondence to Thomas Braulke, braulke{at}uke.uni-hamburg.de.
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G. Makrypidi and M. Damme contributed equally to this article.
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Published ahead of print 12 December 2011
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Supplemental material for this article may be found at http://mcb.asm.org/.
- Copyright © 2012, American Society for Microbiology. All Rights Reserved.












