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10.1038/s41586-020-2332-7 http://scihub22266oqcxt.onion/10.1038/s41586-020-2332-7 32408336!ä!32408336 Deprecated: Implicit conversion from float 227.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 227.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       Nature 2020 ; 583 (7816): 469-472 Nephropedia Template TP {{tp|p=32408336|t=2020. Proteomics of SARS-CoV-2-infected host cells reveals therapy targets |pdf=|usr=}}{{32408336}} gab.com Text Proteomics of SARS-CoV-2-infected host cells reveals therapy targets JO: Nature http://www.kidney.de/pget.php?&tw=1&pmid=32408336 #FOAvip A new coronavirus was recently discovered and named severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Infection with SARS-CoV-2 in humans causes coronavirus disease 2019 (COVID-19) and has been rapidly spreading around the globe(1,2). SARS-CoV-2 shows some similarities to other coronaviruses; however, treatment options and an understanding of how SARS-CoV-2 infects cells are lacking. Here we identify the host cell pathways that are modulated by SARS-CoV-2 and show that inhibition of these pathways prevents viral replication in human cells. We established a human cell-culture model for infection with a clinical isolate of SARS-CoV-2. Using this cell-culture system, we determined the infection profile of SARS-CoV-2 by translatome(3) and proteome proteomics at different times after infection. These analyses revealed that SARS-CoV-2 reshapes central cellular pathways such as translation, splicing, carbon metabolism, protein homeostasis (proteostasis) and nucleic acid metabolism. Small-molecule inhibitors that target these pathways prevented viral replication in cells. Our results reveal the cellular infection profile of SARS-CoV-2 and have enabled the identification of drugs that inhibit viral replication. We anticipate that our results will guide efforts to understand the molecular mechanisms that underlie the modulation of host cells after infection with SARS-CoV-2. Furthermore, our findings provide insights for the development of therapies for the treatment of COVID-19. Twit Text FOAVip Proteomics of SARS-CoV-2-infected host cells reveals therapy targets ????Nature http://www.kidney.de/pget.php?&tw=1&pmid=32408336 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=32408336 #FOAvip English Wikipedia <ref>{{Cite pmid|32408336}}</ref> Proteomics of SARS-CoV-2-infected host cells reveals therapy targets #MMPMID32408336 Bojkova D; Klann K; Koch B; Widera M; Krause D; Ciesek S; Cinatl J; Munch C Nature 2020[Jul]; 583 (7816): 469-472 PMID32408336show ga A new coronavirus was recently discovered and named severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Infection with SARS-CoV-2 in humans causes coronavirus disease 2019 (COVID-19) and has been rapidly spreading around the globe(1,2). SARS-CoV-2 shows some similarities to other coronaviruses; however, treatment options and an understanding of how SARS-CoV-2 infects cells are lacking. Here we identify the host cell pathways that are modulated by SARS-CoV-2 and show that inhibition of these pathways prevents viral replication in human cells. We established a human cell-culture model for infection with a clinical isolate of SARS-CoV-2. Using this cell-culture system, we determined the infection profile of SARS-CoV-2 by translatome(3) and proteome proteomics at different times after infection. These analyses revealed that SARS-CoV-2 reshapes central cellular pathways such as translation, splicing, carbon metabolism, protein homeostasis (proteostasis) and nucleic acid metabolism. Small-molecule inhibitors that target these pathways prevented viral replication in cells. Our results reveal the cellular infection profile of SARS-CoV-2 and have enabled the identification of drugs that inhibit viral replication. We anticipate that our results will guide efforts to understand the molecular mechanisms that underlie the modulation of host cells after infection with SARS-CoV-2. Furthermore, our findings provide insights for the development of therapies for the treatment of COVID-19. |*Molecular Targeted Therapy[MESH] |*Proteomics[MESH] |Betacoronavirus/*drug effects/genetics/growth & development/*metabolism[MESH] |COVID-19[MESH] |COVID-19 Drug Treatment[MESH] |Caco-2 Cells[MESH] |Carbon/metabolism[MESH] |Coronavirus Infections/*drug therapy/genetics/*metabolism/virology[MESH] |Drug Evaluation, Preclinical[MESH] |Host-Pathogen Interactions/drug effects/genetics[MESH] |Humans[MESH] |In Vitro Techniques[MESH] |Kinetics[MESH] |Pandemics[MESH] |Pneumonia, Viral/*drug therapy/genetics/*metabolism/virology[MESH] |Protein Biosynthesis/drug effects[MESH] |Proteome/metabolism[MESH] |Proteostasis[MESH] |RNA Splicing[MESH] |SARS-CoV-2[MESH] |Time Factors[MESH]Proteomics of SARS-CoV-2-infected host cells reveals therapy targets (epmc).pdf DeepDyve Pubget Overpricing