Tracking glideosome-associated protein 50 reveals the development and organization of the inner membrane complex of Plasmodium falciparum

Eukaryotic Cell

Volumn 10, Issue 4, 2011, Pages 556-564

  Yeoman, Jeffrey A ^a   Hanssen, Eric ^a,d   Maier, Alexander G ^a   Klonis, Nectarios ^a   Maco, Bohumil ^a   Baum, Jake ^b   Turnbull, Lynne ^c   Whitchurch, Cynthia B ^c   Dixon, Matthew W A ^a   Tilley, Leann ^a  

^a LA TROBE UNIVERSITY   (Australia)

^b WALTER AND ELIZA HALL INSTITUTE OF MEDICAL RESEARCH   (Australia)

^c UNIVERSITY OF TECHNOLOGY SYDNEY   (Australia)

^d UNIVERSITY OF MELBOURNE   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

GLIDEOSOME ASSOCIATED PROTEIN 45, PLASMODIUM FALCIPARUM; GLIDEOSOME ASSOCIATED PROTEIN 50, PLASMODIUM FALCIPARUM; GLIDEOSOME-ASSOCIATED PROTEIN 45, PLASMODIUM FALCIPARUM; GLIDEOSOME-ASSOCIATED PROTEIN 50, PLASMODIUM FALCIPARUM; HYBRID PROTEIN; MEMBRANE PROTEIN;

ANIMAL; ARTICLE; CELL MEMBRANE; CYTOLOGY; ENDOPLASMIC RETICULUM; GENETICS; HUMAN; MEROZOITE; METABOLISM; PATHOGENICITY; PHYSIOLOGY; PLASMODIUM FALCIPARUM; ULTRASTRUCTURE;

ANIMALS; CELL MEMBRANE; ENDOPLASMIC RETICULUM; HUMANS; MEMBRANE PROTEINS; MEROZOITES; PLASMODIUM FALCIPARUM; RECOMBINANT FUSION PROTEINS;

PLASMODIUM FALCIPARUM;

EID: 79955368787     PISSN: 15359778     EISSN: None     Source Type: Journal    
DOI: 10.1128/EC.00244-10     Document Type: Article

References (42)

1. Abu Bakar, N. A., N. Klonis, E. Hanssen, C. Chan, and L. Tilley. 2010. Digestive-vacuole genesis and endocytic processes in the early intraerythro-cytic stages of Plasmodium falciparum. J. Cell Sci. 123:441-450.
2. Adisa, A., et al. 2007. Re-assessing the locations of components of the classical vesicle-mediated trafficking machinery in transfected Plasmodium falciparum. Int. J. Parasitol. 37:1127-1141.
3. Adisa, A., et al. 2003. The signal sequence of exported protein-1 directs the green fluorescent protein to the parasitophorous vacuole of transfected malaria parasites. J. Biol. Chem. 278:6532-6542.
4. Bannister, L. H., and A. R. Dluzewski. 1990. The ultrastructure of red cell invasion in malaria infections: a review. Blood Cells 16:257-292.
5. Bannister, L. H., J. M. Hopkins, R. E. Fowler, S. Krishna, and G. H. Mitchell. 2000. Ultrastructure of rhoptry development in Plasmodium fal-ciparum erythrocytic schizonts. Parasitology 121:273-287.
6. Bannister, L. H., and G. H. Mitchell. 2009. The malaria merozoite, forty years on. Parasitology 136:1435-1444.
7. Baum, J., T. W. Gilberger, F. Frischknecht, and M. Meissner. 2008. Host-cell invasion by malaria parasites: insights from Plasmodium and Toxo-plasma. Trends Parasitol. 24:557-563.
8. Baum, J., A. T. Papenfuss, B. Baum, T. P. Speed, and A. F. Cowman. 2006. Regulation of apicomplexan actin-based motility. Nat. Rev. Microbiol. 4:621-628.
9. Baum, J., et al. 2006. A conserved molecular motor drives cell invasion and gliding motility across malaria life cycle stages and other apicomplexan parasites. J. Biol. Chem. 281:5197-5208.
10. Bergman, L. W., et al. 2003. Myosin A tail domain interacting protein (MTIP) localizes to the inner membrane complex of Plasmodium sporozo-ites. J. Cell Sci. 116:39-49.
11. Bozdech, Z., et al. 2003. Expression profiling of the schizont and trophozoite stages of Plasmodium falciparum with a long-oligonucleotide microarray. Genome Biol. 4:R9.
12. Bullen, H. E., et al. 2009. A novel family of Apicomplexan glideosome-associated proteins with an inner membrane-anchoring role. J. Biol. Chem. 284:25353-25363.
13. Deitsch, K., C. Driskill, and T. Wellems. 2001. Transformation of malaria parasites by the spontaneous uptake and expression of DNA from human erythrocytes. Nucleic Acids Res. 29:850-853.
14. del Pilar Crespo, M., et al. 2008. Artemisinin and a series of novel endo-peroxide antimalarials exert early effects on digestive vacuole morphology. Antimicrob. Agents Chemother. 52:98-109.
15. de Melo, E. J., and W. de Souza. 1997. A cytochemistry study of the inner membrane complex of the pellicle of tachyzoites of Toxoplasma gondii. Para-sitol. Res. 83:252-256.
16. Dluzewski, A. R., et al. 1992. Origins of the parasitophorous vacuole membrane of the malaria parasite, Plasmodium falciparum, in human red blood cells. J. Cell Sci. 102:527-532.
17. Duraisingh, M. T., A. G. Maier, T. Triglia, and A. F. Cowman. 2003. Eryth-rocyte-binding antigen 175 mediates invasion in Plasmodium falciparum utilizing sialic acid-dependent and -independent pathways. Proc. Natl. Acad. Sci. U.S.A. 100:4796-4801.
18. Fidock, D. A., and T. E. Wellems. 1997. Transformation with human dihy-drofolate reductase renders malaria parasites insensitive to WR99210 but does not affect the intrinsic activity of proguanil. Proc. Natl. Acad. Sci. U. S. A. 94:10931-10936.
19. Frankland, S., et al. 2006. Delivery of the malaria virulence protein PfEMP1 to the erythrocyte surface requires cholesterol-rich domains. Eukaryot. Cell 5:849-860.
20. Gaskins, E., et al. 2004. Identification of the membrane receptor of a class XIV myosin in Toxoplasma gondii. J. Cell Biol. 165:383-393.
21. Gilk, S. D., E. Gaskins, G. E. Ward, and C. J. Beckers. 2009. GAP45 phosphorylation controls assembly of the Toxoplasma myosin XIV complex. Eukaryot. Cell 8:190-196.
22. Green, J. L., et al. 2006. The MTIP-myosin A complex in blood stage malaria parasites. J. Mol. Biol. 355:933-941.
23. Hanssen, E., et al. 2010. Whole cell imaging reveals novel modular features of the exomembrane system of the malaria parasite, Plasmodium falciparum. Int. J. Parasitol. 40:123-134.
24. Hu, G., et al. 2010. Transcriptional profiling of growth perturbations of the human malaria parasite Plasmodium falciparum. Nat. Biotechnol. 28:91-98.
25. Hu, K., et al. 2002. Daughter cell assembly in the protozoan parasite Toxo-plasma gondii. Mol. Biol. Cell 13:593-606.
26. Jones, M. L., E. L. Kitson, and J. C. Rayner. 2006. Plasmodium falciparum erythrocyte invasion: a conserved myosin associated complex. Mol. Biochem. Parasitol. 147:74-84.
27. Keeley, A., and D. Soldati. 2004. The glideosome: a molecular machine powering motility and host-cell invasion by Apicomplexa. Trends Cell Biol. 14:528-532.
28. Klonis, N., et al. 2002. Fluorescence photobleaching analysis for the study of cellular dynamics. Eur. Biophys. J. 31:36-51.
29. Le Roch, K. G., et al. 2003. Discovery of gene function by expression profiling of the malaria parasite life cycle. Science 301:1503-1508.
30. Lingelbach, K., and K. A. Joiner. 1998. The parasitophorous vacuole membrane surrounding Plasmodium and Toxoplasma: an unusual compartment in infected cells. J. Cell Sci. 111:1467-1475.
31. Maier, A. G., et al. 2003. Plasmodium falciparum erythrocyte invasion through glycophorin C and selection for Gerbich negativity in human populations. Nat. Med. 9:87-92.
32. Muller, I. B., et al. 2010. Secretion of an acid phosphatase provides a possible mechanism to acquire host nutrients by Plasmodium falciparum. Cell Micro-biol. 12:677-691.
33. Pinder, J. C., et al. 1998. Actomyosin motor in the merozoite of the malaria parasite, Plasmodium falciparum: implications for red cell invasion. J. Cell Sci. 111:1831-1839.
34. Ranford-Cartwright, L. C., A. Sinha, G. S. Humphreys, and J. M. Mwangi. 2010. New synchronization method for Plasmodium falciparum. Malar. J. 9:170.
35. Rees-Channer, R. R., et al. 2006. Dual acylation of the 45 kDa gliding-associated protein (GAP45) in Plasmodium falciparum merozoites. Mol. Biochem. Parasitol. 149:113-116.
36. Satchell, J. F., et al. 2005. Structure of glyceraldehyde-3-phosphate dehy-drogenase from Plasmodium falciparum. Acta Crystallogr. D Biol. Crystal-logr. 61:1213-1221.
37. Schermelleh, L., et al. 2008. Subdiffraction multicolor imaging of the nuclear periphery with 3D structured illumination microscopy. Science 320:1332-1336.
38. Sim, B. K., C. E. Chitnis, K. Wasniowska, T. J. Hadley, and L. H. Miller. 1994. Receptor and ligand domains for invasion of erythrocytes by Plasmo-dium falciparum. Science 264:1941-1944.
39. Soldati, D., and M. Meissner. 2004. Toxoplasma as a novel system for motility. Curr. Opin. Cell Biol. 16:32-40.
40. Spielmann, T., et al. 2006. A cluster of ring stage-specific genes linked to a locus implicated in cytoadherence in Plasmodium falciparum codes for PEXEL-negative and PEXEL-positive proteins exported into the host cell. Mol. Biol. Cell 17:3613-3624.
41. Topolska, A. E., A. Lidgett, D. Truman, H. Fujioka, and R. L. Coppel. 2004. Characterization of a membrane-associated rhoptry protein of Plasmodium falciparum. J. Biol. Chem. 279:4648-4656.
42. WHO. 2010. World Malaria Report 2010. WHO, Geneva, Switzerland. http://www.who.int/malaria/world_malaria_report_2010/world_malaria_report_2010.pdf.