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30GR

DOTAM-TCB: Universal Small Molecule-Guided Hapten- and T Cell Bispecfic Antibodies for Cancer Immunotherapy

This is a non-PDB format compatible entry.
Summary for 30GR
Entry DOI10.2210/pdb30gr/pdb
DescriptorFAB Fragment Heavy Chain, FAB Fragment Light chain, ~{N}-(5-sulfamoyl-1,3,4-thiadiazol-2-yl)-8-[[4-[[(2~{S})-1,4,7,10-tetrakis(2-azanyl-2-oxidanylidene-ethyl)-1,4,7,10-tetrazacyclododec-2-yl]methyl]phenyl]carbamothioylamino]octanamide, ... (5 entities in total)
Functional Keywordsantibody, fab fragment, dotam, immune system
Biological sourceHomo sapiens
More
Total number of polymer chains2
Total formula weight48329.12
Authors
Ehler, A.,Klein, C.,Surowka, M.,Venetz, D.,Benz, J. (deposition date: 2026-04-24, release date: 2026-10-14)
Primary citationSurowka, M.,Kober, T.,Matscheko, D.,Ehler, A.,Macedo, W.,Assisi, D.,Challier, J.,Sobieniecki, A.,Gianotti, R.,Bransi, A.,Sam, J.,Bonfiglio, J.J.,Wichert, M.,Ricci, A.,Benz, J.,Umana, P.,Venetz, D.,Klein, C.
DOTAM-TCB: Universal Small Molecule-guided Hapten- and T Cell-bispecific Antibodies for Cancer Immunotherapy.
Antib Ther, 9:535-549, 2026
Cited by
PubMed Abstract: Tumor heterogeneity has been identified as a major roadblock for cancer immunotherapy. To overcome this, universal effector cell engagers with interchangeable tumor-targeting adaptors have been developed. Current concepts in this field consist of antibody-based adaptors. Small-molecule (SM) ligands, on the other hand, infiltrate tissues rapidly, have short half-lives, and are potentially orally available. Therefore, we hypothesized that utilizing SM adaptors, combined with effector antibodies, could represent an attractive off-the-shelf therapy.
PubMed: 42824820
DOI: 10.1093/abt/tbag038
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.45 Å)
Structure validation

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