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7U64

Crystal Structure of Anti-Fentanyl Antibody HY6-F9.6 Fab Complexed with Fentanyl

Summary for 7U64
Entry DOI10.2210/pdb7u64/pdb
DescriptorHY6-F9.6 Fab heavy chain, HY6-F9.6 Fab light chain, N-phenyl-N-[1-(2-phenylethyl)piperidin-4-yl]propanamide, ... (6 entities in total)
Functional Keywordsmab, opioid, immune system
Biological sourceMus musculus (Mouse)
More
Total number of polymer chains18
Total formula weight441946.41
Authors
Rodarte, J.V.,Pancera, M.P. (deposition date: 2022-03-03, release date: 2023-01-11, Last modification date: 2024-10-16)
Primary citationRodarte, J.V.,Baehr, C.,Hicks, D.,Liban, T.L.,Weidle, C.,Rupert, P.B.,Jahan, R.,Wall, A.,McGuire, A.T.,Strong, R.K.,Runyon, S.,Pravetoni, M.,Pancera, M.
Structures of drug-specific monoclonal antibodies bound to opioids and nicotine reveal a common mode of binding.
Structure, 31:20-32.e5, 2023
Cited by
PubMed Abstract: Opioid-related fatal overdoses have reached epidemic proportions. Because existing treatments for opioid use disorders offer limited long-term protection, accelerating the development of newer approaches is critical. Monoclonal antibodies (mAbs) are an emerging treatment strategy that targets and sequesters selected opioids in the bloodstream, reducing drug distribution across the blood-brain barrier, thus preventing or reversing opioid toxicity. We previously identified a series of murine mAbs with high affinity and selectivity for oxycodone, morphine, fentanyl, and nicotine. To determine their binding mechanism, we used X-ray crystallography to solve the structures of mAbs bound to their respective targets, to 2.2 Å resolution or higher. Structural analysis showed a critical convergent hydrogen bonding mode that is dependent on a glutamic acid residue in the mAbs' heavy chain and a tertiary amine of the ligand. Characterizing drug-mAb complexes represents a significant step toward rational antibody engineering and future manufacturing activities to support clinical evaluation.
PubMed: 36513069
DOI: 10.1016/j.str.2022.11.008
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.75 Å)
Structure validation

227344

数据于2024-11-13公开中

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