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A CRISPR/Cas9 genetically engineered organoid biobank reveals essential host factors for coronaviruses
by
Clevers, Hans
, Lamers, Mart M.
, Riesebosch, Samra
, Puschhof, Jens
, van den Doel, Petra B.
, de Lau, Wim
, Breugem, Tim I.
, Pleguezuelos-Manzano, Cayetano
, Schipper, Debby
, Mykytyn, Anna Z.
, Geurts, Maarten H.
, Haagmans, Bart L.
, Busslinger, Georg
, Zhang, Jingshu
, Beumer, Joep
, van der Vaart, Jelte
in
13/100
/ 13/106
/ 13/109
/ 13/51
/ 14/19
/ 14/63
/ 38
/ 38/91
/ 45/70
/ 631/1647/1511
/ 631/208/4041/3196
/ 631/326/596/4130
/ 631/532/2118/2437
/ 631/61/2320
/ ACE2
/ Angiotensin-converting enzyme 2
/ Biobanks
/ Biology
/ Cathepsin B
/ Cell lines
/ Cell surface
/ Computer viruses
/ Coronaviridae
/ Coronaviruses
/ COVID-19
/ CRISPR
/ Genes
/ Genetic engineering
/ Genetic screening
/ Humanities and Social Sciences
/ Intestine
/ Middle East respiratory syndrome
/ multidisciplinary
/ Mutants
/ Organoids
/ Protease
/ Proteinase
/ Replication
/ Science
/ Science (multidisciplinary)
/ Severe acute respiratory syndrome coronavirus 2
/ Therapeutic applications
/ Therapeutic targets
/ Viral diseases
2021
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A CRISPR/Cas9 genetically engineered organoid biobank reveals essential host factors for coronaviruses
by
Clevers, Hans
, Lamers, Mart M.
, Riesebosch, Samra
, Puschhof, Jens
, van den Doel, Petra B.
, de Lau, Wim
, Breugem, Tim I.
, Pleguezuelos-Manzano, Cayetano
, Schipper, Debby
, Mykytyn, Anna Z.
, Geurts, Maarten H.
, Haagmans, Bart L.
, Busslinger, Georg
, Zhang, Jingshu
, Beumer, Joep
, van der Vaart, Jelte
in
13/100
/ 13/106
/ 13/109
/ 13/51
/ 14/19
/ 14/63
/ 38
/ 38/91
/ 45/70
/ 631/1647/1511
/ 631/208/4041/3196
/ 631/326/596/4130
/ 631/532/2118/2437
/ 631/61/2320
/ ACE2
/ Angiotensin-converting enzyme 2
/ Biobanks
/ Biology
/ Cathepsin B
/ Cell lines
/ Cell surface
/ Computer viruses
/ Coronaviridae
/ Coronaviruses
/ COVID-19
/ CRISPR
/ Genes
/ Genetic engineering
/ Genetic screening
/ Humanities and Social Sciences
/ Intestine
/ Middle East respiratory syndrome
/ multidisciplinary
/ Mutants
/ Organoids
/ Protease
/ Proteinase
/ Replication
/ Science
/ Science (multidisciplinary)
/ Severe acute respiratory syndrome coronavirus 2
/ Therapeutic applications
/ Therapeutic targets
/ Viral diseases
2021
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A CRISPR/Cas9 genetically engineered organoid biobank reveals essential host factors for coronaviruses
by
Clevers, Hans
, Lamers, Mart M.
, Riesebosch, Samra
, Puschhof, Jens
, van den Doel, Petra B.
, de Lau, Wim
, Breugem, Tim I.
, Pleguezuelos-Manzano, Cayetano
, Schipper, Debby
, Mykytyn, Anna Z.
, Geurts, Maarten H.
, Haagmans, Bart L.
, Busslinger, Georg
, Zhang, Jingshu
, Beumer, Joep
, van der Vaart, Jelte
in
13/100
/ 13/106
/ 13/109
/ 13/51
/ 14/19
/ 14/63
/ 38
/ 38/91
/ 45/70
/ 631/1647/1511
/ 631/208/4041/3196
/ 631/326/596/4130
/ 631/532/2118/2437
/ 631/61/2320
/ ACE2
/ Angiotensin-converting enzyme 2
/ Biobanks
/ Biology
/ Cathepsin B
/ Cell lines
/ Cell surface
/ Computer viruses
/ Coronaviridae
/ Coronaviruses
/ COVID-19
/ CRISPR
/ Genes
/ Genetic engineering
/ Genetic screening
/ Humanities and Social Sciences
/ Intestine
/ Middle East respiratory syndrome
/ multidisciplinary
/ Mutants
/ Organoids
/ Protease
/ Proteinase
/ Replication
/ Science
/ Science (multidisciplinary)
/ Severe acute respiratory syndrome coronavirus 2
/ Therapeutic applications
/ Therapeutic targets
/ Viral diseases
2021
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A CRISPR/Cas9 genetically engineered organoid biobank reveals essential host factors for coronaviruses
Journal Article
A CRISPR/Cas9 genetically engineered organoid biobank reveals essential host factors for coronaviruses
2021
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Overview
Rapid identification of host genes essential for virus replication may expedite the generation of therapeutic interventions. Genetic screens are often performed in transformed cell lines that poorly represent viral target cells in vivo, leading to discoveries that may not be translated to the clinic. Intestinal organoids are increasingly used to model human disease and are amenable to genetic engineering. To discern which host factors are reliable anti-coronavirus therapeutic targets, we generate mutant clonal IOs for 19 host genes previously implicated in coronavirus biology. We verify ACE2 and DPP4 as entry receptors for SARS-CoV/SARS-CoV-2 and MERS-CoV respectively. SARS-CoV-2 replication in IOs does not require the endosomal Cathepsin B/L proteases, but specifically depends on the cell surface protease TMPRSS2. Other TMPRSS family members were not essential. The newly emerging coronavirus variant B.1.1.7, as well as SARS-CoV and MERS-CoV similarly depended on TMPRSS2. These findings underscore the relevance of non-transformed human models for coronavirus research, identify TMPRSS2 as an attractive pan-coronavirus therapeutic target, and demonstrate that an organoid knockout biobank is a valuable tool to investigate the biology of current and future emerging coronaviruses.
Rapid identification of host genes essential for virus replication may expedite the generation of therapeutic interventions. Here the authors generate mutant clonal intestinal organoids for 19 host genes previously implicated in coronavirus biology and identify the cell surface protease TMPRSS2 as a potential therapeutic target.
Publisher
Nature Publishing Group UK,Nature Publishing Group,Nature Portfolio
Subject
/ 13/106
/ 13/109
/ 13/51
/ 14/19
/ 14/63
/ 38
/ 38/91
/ 45/70
/ ACE2
/ Angiotensin-converting enzyme 2
/ Biobanks
/ Biology
/ COVID-19
/ CRISPR
/ Genes
/ Humanities and Social Sciences
/ Middle East respiratory syndrome
/ Mutants
/ Protease
/ Science
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