PubMed:33122196 JSONTXT 39 Projects

Annnotations TAB TSV DIC JSON TextAE

Id Subject Object Predicate Lexical cue
T1 0-90 Sentence denotes High affinity binding of SARS-CoV-2 spike protein enhances ACE2 carboxypeptidase activity.
T2 91-225 Sentence denotes The novel severe acute respiratory syndrome coronavirus (SARS-CoV-2) has emerged to a pandemic and caused global public health crisis.
T3 226-322 Sentence denotes Human angiotensin-converting enzyme 2(ACE2) was identified as the entry receptor for SARS-CoV-2.
T4 323-461 Sentence denotes As a carboxypeptidase, ACE2 cleaves many biological substrates besides angiotensin II to control vasodilatation and vascular permeability.
T5 462-620 Sentence denotes Given the nanomolar high affinity between ACE2 and SARS-CoV-2 spike protein, we investigated how this interaction would affect the enzymatic activity of ACE2.
T6 621-800 Sentence denotes Surprisingly, SARS-CoV-2 trimeric spike protein increased ACE2 proteolytic activity ~3-10 fold against model peptide substrates, such as caspase-1 substrate and Bradykinin-analog.
T7 801-903 Sentence denotes The enhancement in ACE2 enzymatic function was mediated by the binding of SARS-CoV-2 spike RBD domain.
T8 904-1073 Sentence denotes These results highlighted the potential for SARS-CoV-2 infection to enhance ACE2 activity, which may be relevant to the cardiovascular symptoms associated with COVID-19.