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Nobuko Yoshida, P. Potocnjak, Victor Nussenzweig, R. Nussenzweig, J. Rockefeller (1981)
Biosynthesis of Pb44, the protective antigen of sporozoites of Plasmodium bergheiThe Journal of Experimental Medicine, 154
S. Pancake, M. Hollingdale (1986)
Plasmodium berghei: reaction of sporozoites with chemically and enzymatically modified hepatoma cells.Experimental parasitology, 62 1
S. Aley, M. Bates, J. Tam, M. Hollingdale (1986)
Synthetic peptides from the circumsporozoite proteins of Plasmodium falciparum and Plasmodium knowlesi recognize the human hepatoma cell line HepG2-A16 in vitroThe Journal of Experimental Medicine, 164
M. Hollingdale (1985)
Malaria and the liverHepatology, 5
V. Nussenzweig, R. Nussenzweig (1985)
Circumsporozoite proteins of malaria parasitesCell, 42
A. Cochrane, F. Santoro, V. Nussenzweig, R. Gwadz, R. Nussenzweig (1982)
Monoclonal antibodies identify the protective antigens of sporozoites of Plasmodium knowlesi.Proceedings of the National Academy of Sciences of the United States of America, 79 18
M. Aikawa, N. Yoshida, R. Nussenzweig, V. Nussenzweig (1981)
The protective antigen of malarial sporozoites (Plasmodium berghei) is a differentiation antigen.Journal of immunology, 126 6
Drum (1966)
Diatom locomotion: an explanationProtoplasma, 62
M. Stewart, R. Nawrot, S. Schulman, J. Vanderberg (1986)
Plasmodium berghei sporozoite invasion is blocked in vitro by sporozoite-immobilizing antibodiesInfection and Immunity, 51
M. Hollingdale, P. Leland, J. Leef, A. Schwartz (1983)
Entry of Plasmodium berghei sporozoites into cultured cells, and their transformation into trophozoites.The American journal of tropical medicine and hygiene, 32 4
N. Yoshida, R. Nussenzweig, P. Potocnjak, V. Nussenzweig, M. Aikawa (1980)
Hybridoma produces protective antibodies directed against the sporozoite stage of malaria parasite.Science, 207 4426
M. Hollingdale, F. Zavala, R. Nussenzweig, V. Nussenzweig (1982)
Antibodies to the protective antigen of Plasmodium berghei sporozoites prevent entry into cultured cells.Journal of immunology, 128 4
J. Vanderberg, R. Nussenzweig, Harry Most (1969)
Protective immunity produced by the injection of x-irradiated sporozoites of Plasmodium berghei. V. In vitro effects of immune serum on sporozoites.Military medicine, 134 10
P. Potocnjak, N. Yoshida, R. Nussenzweig, V. Nussenzweig (1980)
Monovalent fragments (Fab) of monoclonal antibodies to a sporozoite surface antigen (Pb44) protect mice against malarial infectionThe Journal of Experimental Medicine, 151
E. Nardin, R. Nussenzweig (1978)
Stage-specific antigens on the surface membrane of sporozoites of malaria parasitesNature, 274
J. Vanderberg (1977)
Plasmodium berghei: quantitation of sporozoites injected by mosquitoes feeding on a rodent host.Experimental parasitology, 42 1
M. Stewart, S. Schulman, J. Vanderberg (1987)
In vitro invasion of host cells by Plasmodium berghei sporozoites in serum-free medium.The Journal of parasitology, 73 2
J. Vanderberg (1974)
Studies on the motility of Plasmodium sporozoites.The Journal of protozoology, 21 4
Alan Cochrane, Masamichi Aikawa, Miji Jeng, R. Nussenzweig (1976)
Antibody-induced ultrastructural changes of malarial sporozoites.Journal of immunology, 116 3
R. Burchard (1981)
Gliding motility of prokaryotes: ultrastructure, physiology, and genetics.Annual review of microbiology, 35
As Plasmodium sporozoites undergo gliding motility in vitro, they leave behind trails of circumsporozoite (CS) protein that correspond to their patterns of movement. This light microscopic observation was made using Plasmodium berghei sporozoites, a monoclonal antibody (MAb H4) directed against the immunodominant repetitive epitope of the CS protein of P. berghei, and an immunogold‐silver staining (IGSS) technique. Sporozoites pretreated with agents that inhibit sporozoite motility and invasiveaess did not produce trails. Sporozoites that glided on microscope slides coated with MAb H4 left behind considerably longer CS prolem trails than those on uncoated slides, and the staining of these trails was more intense. The fact that the CS protein is an exoantigen continuously released as trails by motile sporozoites, together with our previous finding that anti‐CS protein antibodies inhibit sporozoite motility, strongly suggests that the CS protein plays a role in gliding motility. The sensitive IGSS technique used in this study may be a useful tool in the study of the translocation of surface proteins during gliding of other apicomplexans, other protists, and bacteria.
The Journal of Eukaryotic Microbiology – Wiley
Published: Aug 1, 1988
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