Table 4.
Potential peptide-based therapeutic efficacy in preclinical platforms
| Potential peptide therapeutic | Target SARS-CoV-2 (COVID-19) | Sequence | Platform | Result |
|---|---|---|---|---|
| EK1 | HR1 domain of CoV S protein (MFM) | SLDQINVTFLDLEYEMKLE EAIKLEESYIDLKEL | Preclinical in vivo models | 100% prophylactic and 80% therapeutic effective in mouse model of HCoV-OC43 (survival analysis) |
| EK1C4 (lipopeptide) | HR1 domain of CoV S protein (MFM) | (N) EK1-GSGSG-PEG4-(Chol) | Preclinical in vitro and in vivo models | 100% prophylactic and 16.7–100% therapeutic effect in HCoV-OC43 infection mouse model |
| IPB02 | HR1 domain of CoV S protein (MFM) | ISGINASVVNIQKEIDRLNE VAKNLNESLIDLQELK (Chol) | Preclinical in vitro models | IPB02 inhibited SARS-CoV-2 S protein-mediated cell–cell fusion and pseudovirus transduction with high potency |
| SBP1 (peptidase domain of ACE2) | S protein-RBD | IEEQAKTFLDKFNHE AEDLFYQS | Preclinical in vitro models | SBP1 interacts with insect-derived SARS-CoV-2-RBD protein obtained from Sino Biologicals with micromolar affinity, according to BLI |
ACE=Angiotensin-converting enzyme, HR=Heptad repeat, RBD=Receptor-binding domain, BLI=Bio-layer interferometry, SARS-CoV-2=Severe acute respiratory syndrome coronavirus 2, EK1, IPB02, SBP1, MFM, GSGSG, PEG4, HCoV-OC43