9Z1N
Structure of KP.3 spike in complex with Nanosota-9B (local refinement)
Summary for 9Z1N
| Entry DOI | 10.2210/pdb9z1n/pdb |
| EMDB information | 73750 |
| Descriptor | KP.3 spike, Nanosota-9B (2 entities in total) |
| Functional Keywords | sars-cov-2, entry, viral protein-immune system complex, viral protein/immune system |
| Biological source | Severe acute respiratory syndrome coronavirus 2 More |
| Total number of polymer chains | 2 |
| Total formula weight | 154616.39 |
| Authors | |
| Primary citation | Bu, F.,Saxena, D.,Turner-Hubbard, H.,Delaney, A.,Batra, L.,Fricke, C.,Moye, S.,Verma, A.,Perlman, S.,Bhandari, J.,Liu, B.,Ye, G.,Zheng, J.,Li, F. Update and reuse: Structure-guided nanobody evolution against SARS-CoV-2 escape. Plos Pathog., 22:e1014223-e1014223, 2026 Cited by PubMed Abstract: SARS-CoV-2 continues to accumulate spike mutations that erode the efficacy of antibody therapeutics. The Q493E mutation in the spike RBD, present in recent Omicron subvariants, enables escape from many antibodies and nanobodies, including our Nanosota-9A nanobody, which neutralizes Omicron JN.1 (Q493) but not KP.3 (E493). To address this, we applied a structure-guided in vitro evolution strategy to engineer Nanosota-9A, generating Nanosota-9B, which binds the KP.3 RBD with high affinity but shows reduced binding to JN.1 RBD. To regain breadth, we engineered a bispecific nanobody combining Nanosota-9A and -9B, which effectively neutralizes both JN.1 and KP.3 in infection assays. Our results provide proof of concept for an "update and reuse" strategy: applying structure-guided engineering to update and reuse validated nanobodies to overcome variant escape. This strategy offers a practical path to maintain therapeutic coverage as the virus evolves, supporting more efficient use of research resources and faster responses to emerging variants. PubMed: 42149970DOI: 10.1371/journal.ppat.1014223 PDB entries with the same primary citation |
| Experimental method | ELECTRON MICROSCOPY (3.44 Å) |
Structure validation
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