tetano
Editor, Senior Moderator
J Biol Chem
. 2022 Oct 26;102643.
doi: 10.1016/j.jbc.2022.102643. Online ahead of print.
Transmembrane serine protease TMPRSS2 implicated in SARS-CoV-2 infection is autoactivated intracellularly and requires N-glycosylation for regulation
Yikai Zhang[SUP] 1 [/SUP], Shijin Sun[SUP] 1 [/SUP], Chunyu Du[SUP] 2 [/SUP], Kaixuan Hu[SUP] 2 [/SUP], Ce Zhang[SUP] 1 [/SUP], Meng Liu[SUP] 1 [/SUP], Qingyu Wu[SUP] 3 [/SUP], Ningzheng Dong[SUP] 4 [/SUP]
Affiliations
Abstract
Transmembrane protease serine 2 (TMPRSS2) is a membrane-bound protease expressed in many human epithelial tissues, including the airway and lung. TMPRSS2-mediated cleavage of viral spike (S) protein is a key mechanism in severe acute respiratory syndrome (SARS) coronavirus (CoV)-2 activation and host cell entry. To date, the cellular mechanisms that regulate TMPRSS2 activity and cell surface expression are not fully characterized. In this study, we examined two major posttranslational events, zymogen activation and N-glycosylation, in human TMPRSS2. In experiments with human embryonic kidney 293 (HEK293), bronchial epithelial 16HBE, and lung alveolar epithelial A549 cells, we found that TMPRSS2 was activated via intracellular autocatalysis and that this process was blocked in the presence of hepatocyte growth factor activator inhibitors 1 and 2. By glycosidase digestion and site-directed mutagenesis, we showed that human TMPRSS2 was N-glycosylated. N-glycosylation at an evolutionarily conserved site in the scavenger receptor cysteine-rich domain was required for calnexin-assisted protein folding in the ER and subsequent intracellular trafficking, zymogen activation, and cell surface expression. Moreover, we showed that TMPRSS2 cleaved SARS-CoV-2 S protein intracellularly in HEK293 cells. These results provide new insights into the cellular mechanism in regulating TMPRSS2 biosynthesis and function. Our findings should help to understand the role of TMPRSS2 in major respiratory viral diseases.
Keywords: HAI-1; HAI-2; N-glycosylation; SARS-CoV-2; TMPRSS2; TTSP; spike protein; zymogen activation.
. 2022 Oct 26;102643.
doi: 10.1016/j.jbc.2022.102643. Online ahead of print.
Transmembrane serine protease TMPRSS2 implicated in SARS-CoV-2 infection is autoactivated intracellularly and requires N-glycosylation for regulation
Yikai Zhang[SUP] 1 [/SUP], Shijin Sun[SUP] 1 [/SUP], Chunyu Du[SUP] 2 [/SUP], Kaixuan Hu[SUP] 2 [/SUP], Ce Zhang[SUP] 1 [/SUP], Meng Liu[SUP] 1 [/SUP], Qingyu Wu[SUP] 3 [/SUP], Ningzheng Dong[SUP] 4 [/SUP]
Affiliations
- PMID: 36309092
- DOI: 10.1016/j.jbc.2022.102643
Abstract
Transmembrane protease serine 2 (TMPRSS2) is a membrane-bound protease expressed in many human epithelial tissues, including the airway and lung. TMPRSS2-mediated cleavage of viral spike (S) protein is a key mechanism in severe acute respiratory syndrome (SARS) coronavirus (CoV)-2 activation and host cell entry. To date, the cellular mechanisms that regulate TMPRSS2 activity and cell surface expression are not fully characterized. In this study, we examined two major posttranslational events, zymogen activation and N-glycosylation, in human TMPRSS2. In experiments with human embryonic kidney 293 (HEK293), bronchial epithelial 16HBE, and lung alveolar epithelial A549 cells, we found that TMPRSS2 was activated via intracellular autocatalysis and that this process was blocked in the presence of hepatocyte growth factor activator inhibitors 1 and 2. By glycosidase digestion and site-directed mutagenesis, we showed that human TMPRSS2 was N-glycosylated. N-glycosylation at an evolutionarily conserved site in the scavenger receptor cysteine-rich domain was required for calnexin-assisted protein folding in the ER and subsequent intracellular trafficking, zymogen activation, and cell surface expression. Moreover, we showed that TMPRSS2 cleaved SARS-CoV-2 S protein intracellularly in HEK293 cells. These results provide new insights into the cellular mechanism in regulating TMPRSS2 biosynthesis and function. Our findings should help to understand the role of TMPRSS2 in major respiratory viral diseases.
Keywords: HAI-1; HAI-2; N-glycosylation; SARS-CoV-2; TMPRSS2; TTSP; spike protein; zymogen activation.