Application | Comment | Organism |
---|---|---|
medicine | SARS spike (S) protein cleavage by TMPRSS2 decreases viral sensitivity to inhibition by neutralizing antibodies, and TMPRSS2-dependent SARS S shedding confers resistance against antibody-mediated neutralization. TMPRSS2 cleaves and activates SARS S in trans. TMPRSS2 on target cells allows efficient SARS S-driven virus-cell fusion in the presence of a lysosomotropic agent and a cathepsin inhibitor | Homo sapiens |
Localization | Comment | Organism | GeneOntology No. | Textmining |
---|---|---|---|---|
membrane | - |
Homo sapiens | 16020 | - |
Organism | UniProt | Comment | Textmining |
---|---|---|---|
Homo sapiens | O15393 | - |
- |
Source Tissue | Comment | Organism | Textmining |
---|---|---|---|
lung | - |
Homo sapiens | - |
Substrates | Comment Substrates | Organism | Products | Comment (Products) | Rev. | Reac. |
---|---|---|---|---|---|---|
SARS coronavirus spike protein + H2O | - |
Homo sapiens | ? | - |
? |
General Information | Comment | Organism |
---|---|---|
physiological function | SARS spike (S) protein is cleaved into several fragments upon coexpression of TMPRSS2 (cis-cleavage) and upon contact between SARS S-expressing cells and TMPRSS2-positive cells (trans-cleavage). cis-Cleavage results in release of SARS S fragments into the cellular supernatant and in inhibition of antibody-mediated neutralization. trans-Cleavage activates SARS S on effector cells for fusion with target cells and allows efficient SARS S-driven viral entry into targets treated with a lysosomotropic agent or a cathepsin inhibitor. ACE2, the cellular receptor for SARSCoV, and TMPRSS2 are coexpressed by type II pneumocytes | Homo sapiens |