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A trimeric human angiotensin-converting enzyme 2 as an anti-SARS-CoV-2 agent
by
Johnson, Rebecca I.
, Lu, Jianming
, McKay, Lindsay G. A.
, Chen, Bing
, Lu, Shen
, Lavine, Christy L.
, Rits-Volloch, Sophia
, Quinlan, Brian D.
, Seaman, Michael S.
, Griffiths, Anthony
, Xiao, Tianshu
, Farzan, Michael
, Peng, Hanqin
, Storm, Nadia
, Cai, Yongfei
, Zhang, Jun
in
13
/ 631/45
/ 631/535
/ 82
/ ACE2
/ Affinity
/ Angiotensin
/ Angiotensin II
/ Angiotensin-converting enzyme 2
/ Angiotensin-Converting Enzyme 2 - chemistry
/ Angiotensin-Converting Enzyme 2 - genetics
/ Angiotensin-Converting Enzyme 2 - therapeutic use
/ Antiviral Agents - chemistry
/ Antiviral Agents - therapeutic use
/ Biochemistry
/ Biological Microscopy
/ Biomedical and Life Sciences
/ Carboxypeptidase
/ Cell culture
/ Conversion
/ Coronaviruses
/ COVID-19
/ COVID-19 Drug Treatment
/ Cryoelectron Microscopy
/ Dimers
/ Enzymatic activity
/ Enzymes
/ Humans
/ Life Sciences
/ Membrane Biology
/ Models, Molecular
/ Pandemics
/ Peptidase
/ Peptidases
/ Peptidyl-dipeptidase A
/ Protein Engineering
/ Protein Multimerization
/ Protein Structure
/ Receptors
/ Recombinant Proteins - chemistry
/ Recombinant Proteins - genetics
/ Recombinant Proteins - therapeutic use
/ Renin
/ Respiratory diseases
/ SARS-CoV-2 - physiology
/ Severe acute respiratory syndrome coronavirus 2
/ Spike protein
/ Viral diseases
2021
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A trimeric human angiotensin-converting enzyme 2 as an anti-SARS-CoV-2 agent
by
Johnson, Rebecca I.
, Lu, Jianming
, McKay, Lindsay G. A.
, Chen, Bing
, Lu, Shen
, Lavine, Christy L.
, Rits-Volloch, Sophia
, Quinlan, Brian D.
, Seaman, Michael S.
, Griffiths, Anthony
, Xiao, Tianshu
, Farzan, Michael
, Peng, Hanqin
, Storm, Nadia
, Cai, Yongfei
, Zhang, Jun
in
13
/ 631/45
/ 631/535
/ 82
/ ACE2
/ Affinity
/ Angiotensin
/ Angiotensin II
/ Angiotensin-converting enzyme 2
/ Angiotensin-Converting Enzyme 2 - chemistry
/ Angiotensin-Converting Enzyme 2 - genetics
/ Angiotensin-Converting Enzyme 2 - therapeutic use
/ Antiviral Agents - chemistry
/ Antiviral Agents - therapeutic use
/ Biochemistry
/ Biological Microscopy
/ Biomedical and Life Sciences
/ Carboxypeptidase
/ Cell culture
/ Conversion
/ Coronaviruses
/ COVID-19
/ COVID-19 Drug Treatment
/ Cryoelectron Microscopy
/ Dimers
/ Enzymatic activity
/ Enzymes
/ Humans
/ Life Sciences
/ Membrane Biology
/ Models, Molecular
/ Pandemics
/ Peptidase
/ Peptidases
/ Peptidyl-dipeptidase A
/ Protein Engineering
/ Protein Multimerization
/ Protein Structure
/ Receptors
/ Recombinant Proteins - chemistry
/ Recombinant Proteins - genetics
/ Recombinant Proteins - therapeutic use
/ Renin
/ Respiratory diseases
/ SARS-CoV-2 - physiology
/ Severe acute respiratory syndrome coronavirus 2
/ Spike protein
/ Viral diseases
2021
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A trimeric human angiotensin-converting enzyme 2 as an anti-SARS-CoV-2 agent
by
Johnson, Rebecca I.
, Lu, Jianming
, McKay, Lindsay G. A.
, Chen, Bing
, Lu, Shen
, Lavine, Christy L.
, Rits-Volloch, Sophia
, Quinlan, Brian D.
, Seaman, Michael S.
, Griffiths, Anthony
, Xiao, Tianshu
, Farzan, Michael
, Peng, Hanqin
, Storm, Nadia
, Cai, Yongfei
, Zhang, Jun
in
13
/ 631/45
/ 631/535
/ 82
/ ACE2
/ Affinity
/ Angiotensin
/ Angiotensin II
/ Angiotensin-converting enzyme 2
/ Angiotensin-Converting Enzyme 2 - chemistry
/ Angiotensin-Converting Enzyme 2 - genetics
/ Angiotensin-Converting Enzyme 2 - therapeutic use
/ Antiviral Agents - chemistry
/ Antiviral Agents - therapeutic use
/ Biochemistry
/ Biological Microscopy
/ Biomedical and Life Sciences
/ Carboxypeptidase
/ Cell culture
/ Conversion
/ Coronaviruses
/ COVID-19
/ COVID-19 Drug Treatment
/ Cryoelectron Microscopy
/ Dimers
/ Enzymatic activity
/ Enzymes
/ Humans
/ Life Sciences
/ Membrane Biology
/ Models, Molecular
/ Pandemics
/ Peptidase
/ Peptidases
/ Peptidyl-dipeptidase A
/ Protein Engineering
/ Protein Multimerization
/ Protein Structure
/ Receptors
/ Recombinant Proteins - chemistry
/ Recombinant Proteins - genetics
/ Recombinant Proteins - therapeutic use
/ Renin
/ Respiratory diseases
/ SARS-CoV-2 - physiology
/ Severe acute respiratory syndrome coronavirus 2
/ Spike protein
/ Viral diseases
2021
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A trimeric human angiotensin-converting enzyme 2 as an anti-SARS-CoV-2 agent
Journal Article
A trimeric human angiotensin-converting enzyme 2 as an anti-SARS-CoV-2 agent
2021
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Overview
Effective intervention strategies are urgently needed to control the COVID-19 pandemic. Human angiotensin-converting enzyme 2 (ACE2) is a membrane-bound carboxypeptidase that forms a dimer and serves as the cellular receptor for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). ACE2 is also a key negative regulator of the renin–angiotensin system that modulates vascular functions. We report here the properties of a trimeric ACE2 ectodomain variant, engineered using a structure-based approach. The trimeric ACE2 variant has a binding affinity of ~60 pM for the spike protein of SARS‑CoV‑2 (compared with 77 nM for monomeric ACE2 and 12–22 nM for dimeric ACE2 constructs), and its peptidase activity and the ability to block activation of angiotensin II receptor type 1 in the renin–angiotensin system are preserved. Moreover, the engineered ACE2 potently inhibits SARS‑CoV‑2 infection in cell culture. These results suggest that engineered, trimeric ACE2 may be a promising anti-SARS-CoV-2 agent for treating COVID-19.
Engineered soluble trimeric ACE2 constructs with intact enzymatic activity and high affinity to SARS-CoV-2 spike are shown to inhibit viral infection in cellular assays.
Publisher
Nature Publishing Group US,Nature Publishing Group
Subject
/ 631/45
/ 631/535
/ 82
/ ACE2
/ Affinity
/ Angiotensin-converting enzyme 2
/ Angiotensin-Converting Enzyme 2 - chemistry
/ Angiotensin-Converting Enzyme 2 - genetics
/ Angiotensin-Converting Enzyme 2 - therapeutic use
/ Antiviral Agents - chemistry
/ Antiviral Agents - therapeutic use
/ Biomedical and Life Sciences
/ COVID-19
/ Dimers
/ Enzymes
/ Humans
/ Recombinant Proteins - chemistry
/ Recombinant Proteins - genetics
/ Recombinant Proteins - therapeutic use
/ Renin
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