Xin-zhu Chen, Rui-xue Bai, Fei-yu Qin, Hong-juan Peng, Jin-feng Ren, Lang Hu, Yu-di Li, Cheng He
{"title":"磷酸蛋白质组学分析揭示了弓形虫增殖的主要细胞过程和相关的关键磷酸蛋白。","authors":"Xin-zhu Chen, Rui-xue Bai, Fei-yu Qin, Hong-juan Peng, Jin-feng Ren, Lang Hu, Yu-di Li, Cheng He","doi":"10.1007/s11686-023-00720-y","DOIUrl":null,"url":null,"abstract":"<div><h3>Purpose</h3><p>To explore the essential roles of phosphorylation in mediating the proliferation of <i>T. gondii</i> in its cell lytic life.</p><h3>Methods</h3><p>We profiled the phosphoproteome data of <i>T. gondii</i> residing in HFF cells for 2 h and 6 h, representing the early- and late-stages of proliferation (ESP and LSP) within its first generation of division.</p><h3>Results</h3><p>We identified 70 phosphoproteins, among which 8 phosphoproteins were quantified with the phosphorylation level significantly regulated. While only two of the eight phosphoproteins, GRA7 and TGGT1_242070, were significantly down-regulated at the transcriptional level in the group of LSP vs. ESP. Moreover, GO terms correlated with host membrane component were significantly enriched in the category of cellular component, suggesting phosphoprotein played important roles in acquiring essential substance from host cell via manipulating host membrane. Further GO analysis in the categories of molecular function and biological process and pathway analysis revealed that the cellular processes of glucose and lipid metabolism were regulated by <i>T. gondii</i> phosphoproteins such as PMCAA1, LIPIN, Pyk1 and ALD. Additionally, several phosphoproteins were enriched at the central nodes in the protein–protein interaction network, which may have essential roles in <i>T. gondii</i> proliferation including GAP45, MLC1, fructose-1,6-bisphosphate aldolase, GRAs and so on.</p><h3>Conclusion</h3><p>This study revealed the main cellular processes and key phosphoproteins crucial for the intracellular proliferation of <i>T. gondii</i>, which would provide clues to explore the roles of phosphorylation in regulating the development of tachyzoites and new insight into the mechanism of <i>T. gondii</i> development <i>in vitro</i>.</p></div>","PeriodicalId":6932,"journal":{"name":"Acta Parasitologica","volume":"68 4","pages":"820 - 831"},"PeriodicalIF":1.2000,"publicationDate":"2023-10-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Phosphoproteomic Analysis Reveals the Predominating Cellular Processes and the Involved Key Phosphoproteins Essential for the Proliferation of Toxoplasma gondii\",\"authors\":\"Xin-zhu Chen, Rui-xue Bai, Fei-yu Qin, Hong-juan Peng, Jin-feng Ren, Lang Hu, Yu-di Li, Cheng He\",\"doi\":\"10.1007/s11686-023-00720-y\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Purpose</h3><p>To explore the essential roles of phosphorylation in mediating the proliferation of <i>T. gondii</i> in its cell lytic life.</p><h3>Methods</h3><p>We profiled the phosphoproteome data of <i>T. gondii</i> residing in HFF cells for 2 h and 6 h, representing the early- and late-stages of proliferation (ESP and LSP) within its first generation of division.</p><h3>Results</h3><p>We identified 70 phosphoproteins, among which 8 phosphoproteins were quantified with the phosphorylation level significantly regulated. While only two of the eight phosphoproteins, GRA7 and TGGT1_242070, were significantly down-regulated at the transcriptional level in the group of LSP vs. ESP. Moreover, GO terms correlated with host membrane component were significantly enriched in the category of cellular component, suggesting phosphoprotein played important roles in acquiring essential substance from host cell via manipulating host membrane. Further GO analysis in the categories of molecular function and biological process and pathway analysis revealed that the cellular processes of glucose and lipid metabolism were regulated by <i>T. gondii</i> phosphoproteins such as PMCAA1, LIPIN, Pyk1 and ALD. Additionally, several phosphoproteins were enriched at the central nodes in the protein–protein interaction network, which may have essential roles in <i>T. gondii</i> proliferation including GAP45, MLC1, fructose-1,6-bisphosphate aldolase, GRAs and so on.</p><h3>Conclusion</h3><p>This study revealed the main cellular processes and key phosphoproteins crucial for the intracellular proliferation of <i>T. gondii</i>, which would provide clues to explore the roles of phosphorylation in regulating the development of tachyzoites and new insight into the mechanism of <i>T. gondii</i> development <i>in vitro</i>.</p></div>\",\"PeriodicalId\":6932,\"journal\":{\"name\":\"Acta Parasitologica\",\"volume\":\"68 4\",\"pages\":\"820 - 831\"},\"PeriodicalIF\":1.2000,\"publicationDate\":\"2023-10-11\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Acta Parasitologica\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://link.springer.com/article/10.1007/s11686-023-00720-y\",\"RegionNum\":3,\"RegionCategory\":\"农林科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"PARASITOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Acta Parasitologica","FirstCategoryId":"3","ListUrlMain":"https://link.springer.com/article/10.1007/s11686-023-00720-y","RegionNum":3,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"PARASITOLOGY","Score":null,"Total":0}
Phosphoproteomic Analysis Reveals the Predominating Cellular Processes and the Involved Key Phosphoproteins Essential for the Proliferation of Toxoplasma gondii
Purpose
To explore the essential roles of phosphorylation in mediating the proliferation of T. gondii in its cell lytic life.
Methods
We profiled the phosphoproteome data of T. gondii residing in HFF cells for 2 h and 6 h, representing the early- and late-stages of proliferation (ESP and LSP) within its first generation of division.
Results
We identified 70 phosphoproteins, among which 8 phosphoproteins were quantified with the phosphorylation level significantly regulated. While only two of the eight phosphoproteins, GRA7 and TGGT1_242070, were significantly down-regulated at the transcriptional level in the group of LSP vs. ESP. Moreover, GO terms correlated with host membrane component were significantly enriched in the category of cellular component, suggesting phosphoprotein played important roles in acquiring essential substance from host cell via manipulating host membrane. Further GO analysis in the categories of molecular function and biological process and pathway analysis revealed that the cellular processes of glucose and lipid metabolism were regulated by T. gondii phosphoproteins such as PMCAA1, LIPIN, Pyk1 and ALD. Additionally, several phosphoproteins were enriched at the central nodes in the protein–protein interaction network, which may have essential roles in T. gondii proliferation including GAP45, MLC1, fructose-1,6-bisphosphate aldolase, GRAs and so on.
Conclusion
This study revealed the main cellular processes and key phosphoproteins crucial for the intracellular proliferation of T. gondii, which would provide clues to explore the roles of phosphorylation in regulating the development of tachyzoites and new insight into the mechanism of T. gondii development in vitro.
期刊介绍:
Acta Parasitologica is an international journal covering the latest advances in the subject.
Acta Parasitologica publishes original papers on all aspects of parasitology and host-parasite relationships, including the latest discoveries in biochemical and molecular biology of parasites, their physiology, morphology, taxonomy and ecology, as well as original research papers on immunology, pathology, and epidemiology of parasitic diseases in the context of medical, veterinary and biological sciences. The journal also publishes short research notes, invited review articles, book reviews.
The journal was founded in 1953 as "Acta Parasitologica Polonica" by the Polish Parasitological Society and since 1954 has been published by W. Stefanski Institute of Parasitology of the Polish Academy of Sciences in Warsaw. Since 1992 in has appeared as Acta Parasitologica in four issues per year.