The AP3 adaptor is involved in the transport of membrane proteins to acidocalcisomes of Leishmania
Besteiro, Sébastien and Tonn, Daniela and Tetley, L. and Coombs, G.H. and Mottram, J.C. (2008) The AP3 adaptor is involved in the transport of membrane proteins to acidocalcisomes of Leishmania. Journal of Cell Science, 121. pp. 561-570. ISSN 0021-9533 (http://dx.doi.org/10.1242/jcs.022574)
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Lysosomal function is crucial for the differentiation and infectivity of the parasitic protozoon Leishmania major. To study lysosomal biogenesis, an L. major mutant deficient in the subunit of the adaptor protein 3 (AP3 ) complex was generated. Structure and proteolytic capacity of the lysosomal compartment were apparently unaffected in the AP3-deficient mutant; however, defects were identified in its acidocalcisomes. These are acidic organelles enriched in calcium and phosphorus, conserved from bacteria to eukaryotes, whose function remains enigmatic. The acidocalcisomes of the L. major mutant lacked membrane-bound proton pumps (notably V-H+-PPase), were less acidic than normal acidocalcisomes and devoid of polyphosphate, but contained a soluble pyrophosphatase. The mutant parasites were viable in vitro, but were unable to establish an infection in mice, which indicates a role for AP3 in determining - possibly through an acidocalcisome-related function - the virulence of the parasite. AP3 transport function has been linked previously to lysosome-related organelles such as platelet dense granules, which appear to share several features with acidocalcisomes. Our findings, implicating that AP3 has a role in transport to acidocalcisomes, thus provide further evidence that biogenesis of acidocalcisomes resembles that of lysosome-related organelles, and that both may have conserved origins.
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Item type: Article ID code: 12949 Dates: DateEvent2008PublishedSubjects: Medicine > Therapeutics. Pharmacology
Medicine > Pharmacy and materia medica
Science > MicrobiologyDepartment: Faculty of Science > Strathclyde Institute of Pharmacy and Biomedical Sciences Depositing user: Ms Ann Barker-Myles Date deposited: 26 Aug 2009 10:46 Last modified: 20 Jun 2024 20:47 URI: https://strathprints.strath.ac.uk/id/eprint/12949