{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Bi Z"],"funding":["Sichuan Provincial Natural Science Foundation for Young Scholars","China Postdoctoral Science Foundation","The National Science Foundation for Excellent Young Scholars","National Natural Science Foundation Regional Innovation and Development"],"pagination":["e70060"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC12686126"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["58(12)"],"pubmed_abstract":["Continual evolution of SARS-CoV-2 spike drives the emergence of Omicron variants that show increased spreading and immune evasion. Understanding how the variants orientate themselves towards host immune defence is crucial for controlling future pandemics. Herein, we demonstrate that human cathelicidin LL-37, a crucial component of innate immunity, predominantly binds to the S2 subunit of SARS-CoV-2 spike protein, occupying sites where TMPRSS2 typically binds. This binding impedes TMPRSS2-mediated priming at site S2' and subsequent membrane fusion processes. The mutation N764K within S2 subunit of Omicron variants reduces affinity for LL-37 significantly, thereby diminishing binding capacity and inhibitory effects on membrane fusion. Moreover, the early humoral immune response enhanced by L"],"journal":["Cell proliferation"],"pubmed_title":["LL-37 Inhibits TMPRSS2-Mediated S2' Site Cleavage and SARS-CoV-2 Infection but Not Omicron Variants."],"pmcid":["PMC12686126"],"funding_grant_id":["U19A2003","32122052","2022M712244","2024NSFSC1748"],"pubmed_authors":["Ren W","Liu J","Lu G","Chen Z","Zhang X","He X","Zeng H","Wei X","Zhou Y","Wei Y","Bi Z"],"additional_accession":[]},"is_claimable":false,"name":"LL-37 Inhibits TMPRSS2-Mediated S2' Site Cleavage and SARS-CoV-2 Infection but Not Omicron Variants.","description":"Continual evolution of SARS-CoV-2 spike drives the emergence of Omicron variants that show increased spreading and immune evasion. Understanding how the variants orientate themselves towards host immune defence is crucial for controlling future pandemics. Herein, we demonstrate that human cathelicidin LL-37, a crucial component of innate immunity, predominantly binds to the S2 subunit of SARS-CoV-2 spike protein, occupying sites where TMPRSS2 typically binds. This binding impedes TMPRSS2-mediated priming at site S2' and subsequent membrane fusion processes. The mutation N764K within S2 subunit of Omicron variants reduces affinity for LL-37 significantly, thereby diminishing binding capacity and inhibitory effects on membrane fusion. Moreover, the early humoral immune response enhanced by L","dates":{"release":"2025-01-01T00:00:00Z","publication":"2025 Dec","modification":"2026-06-06T01:05:08.898Z","creation":"2026-05-24T03:12:23.892Z"},"accession":"S-EPMC12686126","cross_references":{"pubmed":["40375579"],"doi":["10.1111/cpr.70060"]}}