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Analysis of expression of PDCP and MAL13P1.308 of Plasmodium falciparum: employing a quantitative proteomics approach based on SILAC - Couverture souple
Synopsis
Plasmodium falciparum is a deadly parasite that causes malaria in humans. This disease causes the death of one million people every year. To find new means to fight this parasite, it is important to learn more about its biology. As the pathways of protein expression are better understood, it becomes easier to find out how to block these mechanisms. The completion of the genome sequencing has opened new perspective of genome wide analysis. The yeast-two-hybrid system was used to map the complete interaction network between proteins of P. falciparum. In this protein network of interaction, PDCP is closely related to MSP-1, a protein involved in erythrocyte invasion. PDCP is a CCCH-type zinc finger protein, a family of proteins that are involved in protein-protein interaction, nucleic acid binding and binding in small ligands. It was shown that its expression was dependant on the density of the parasites. In this study we used the SILAC technology to confirm these previous results. Cultures with different parasitemia are grown with heavy isoleucine and analyzed by mass spectrometry.
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Plasmodium falciparum is a deadly parasite that causes malaria in humans. This disease causes the death of one million people every year. To find new means to fight this parasite, it is important to learn more about its biology. As the pathways of protein expression are better understood, it becomes easier to find out how to block these mechanisms. The completion of the genome sequencing has opened new perspective of genome wide analysis. The yeast-two-hybrid system was used to map the complete interaction network between proteins of P. falciparum. In this protein network of interaction, PDCP is closely related to MSP-1, a protein involved in erythrocyte invasion. PDCP is a CCCH-type zinc finger protein, a family of proteins that are involved in protein-protein interaction, nucleic acid binding and binding in small ligands. It was shown that its expression was dependant on the density of the parasites. In this study we used the SILAC technology to confirm these previous results. Cultures with different parasitemia are grown with heavy isoleucine and analyzed by mass spectrometry.
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Analysis of expression of PDCP and MAL13P1.308 of Plasmodium falciparum
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LAP LAMBERT Academic Publishing Apr 2010, 2010
ISBN 10 : 3838357353
ISBN 13 : 9783838357355
Neuf
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Vendeur : BuchWeltWeit Ludwig Meier e.K., Bergisch Gladbach, Allemagne
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Taschenbuch. Etat : Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -Plasmodium falciparum is a deadly parasite that causes malaria in humans. This disease causes the death of one million people every year. To find new means to fight this parasite, it is important to learn more about its biology. As the pathways of protein expression are better understood, it becomes easier to find out how to block these mechanisms. The completion of the genome sequencing has opened new perspective of genome wide analysis. The yeast-two-hybrid system was used to map the complete interaction network between proteins of P. falciparum. In this protein network of interaction, PDCP is closely related to MSP-1, a protein involved in erythrocyte invasion. PDCP is a CCCH-type zinc finger protein, a family of proteins that are involved in protein-protein interaction, nucleic acid binding and binding in small ligands. It was shown that its expression was dependant on the density of the parasites. In this study we used the SILAC technology to confirm these previous results. Cultures with different parasitemia are grown with heavy isoleucine and analyzed by mass spectrometry. 80 pp. Englisch. N° de réf. du vendeur 9783838357355
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Analysis of expression of PDCP and MAL13P1.308 of Plasmodium falciparum
Edité par
LAP LAMBERT Academic Publishing, 2010
ISBN 10 : 3838357353
ISBN 13 : 9783838357355
Neuf
Couverture souple
Vendeur : moluna, Greven, Allemagne
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Analysis of expression of PDCP and MAL13P1.308 of Plasmodium falciparum
Edité par
LAP LAMBERT Academic Publishing Apr 2010, 2010
ISBN 10 : 3838357353
ISBN 13 : 9783838357355
Neuf
Taschenbuch
Vendeur : buchversandmimpf2000, Emtmannsberg, BAYE, Allemagne
Évaluation du vendeur 5 sur 5 étoiles
Taschenbuch. Etat : Neu. Neuware -Plasmodium falciparum is a deadly parasite that causes malaria in humans. This disease causes the death of one million people every year. To find new means to fight this parasite, it is important to learn more about its biology. As the pathways of protein expression are better understood, it becomes easier to find out how to block these mechanisms. The completion of the genome sequencing has opened new perspective of genome wide analysis. The yeast-two-hybrid system was used to map the complete interaction network between proteins of P. falciparum. In this protein network of interaction, PDCP is closely related to MSP-1, a protein involved in erythrocyte invasion. PDCP is a CCCH-type zinc finger protein, a family of proteins that are involved in protein-protein interaction, nucleic acid binding and binding in small ligands. It was shown that its expression was dependant on the density of the parasites. In this study we used the SILAC technology to confirm these previous results. Cultures with different parasitemia are grown with heavy isoleucine and analyzed by mass spectrometry.Books on Demand GmbH, Überseering 33, 22297 Hamburg 80 pp. Englisch. N° de réf. du vendeur 9783838357355
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Analysis of expression of PDCP and MAL13P1.308 of Plasmodium falciparum : employing a quantitative proteomics approach based on SILAC
Edité par
LAP LAMBERT Academic Publishing, 2010
ISBN 10 : 3838357353
ISBN 13 : 9783838357355
Neuf
Taschenbuch
Vendeur : AHA-BUCH GmbH, Einbeck, Allemagne
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Taschenbuch. Etat : Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - Plasmodium falciparum is a deadly parasite that causes malaria in humans. This disease causes the death of one million people every year. To find new means to fight this parasite, it is important to learn more about its biology. As the pathways of protein expression are better understood, it becomes easier to find out how to block these mechanisms. The completion of the genome sequencing has opened new perspective of genome wide analysis. The yeast-two-hybrid system was used to map the complete interaction network between proteins of P. falciparum. In this protein network of interaction, PDCP is closely related to MSP-1, a protein involved in erythrocyte invasion. PDCP is a CCCH-type zinc finger protein, a family of proteins that are involved in protein-protein interaction, nucleic acid binding and binding in small ligands. It was shown that its expression was dependant on the density of the parasites. In this study we used the SILAC technology to confirm these previous results. Cultures with different parasitemia are grown with heavy isoleucine and analyzed by mass spectrometry. N° de réf. du vendeur 9783838357355
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