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7T86

Crystal Structure of Fab CR5133 / Phospho-SD Peptide Complex

Summary for 7T86
Entry DOI10.2210/pdb7t86/pdb
DescriptorAntibody Fab CR5133 Light Chain, Antibody Fab CR5133 Heavy Chain, Phospho-SD Peptide, ... (5 entities in total)
Functional Keywordsstaphylcoccus aureus, sd repeat, phospho sd peptide, fab, cr5133, toxin
Biological sourceHomo sapiens
More
Total number of polymer chains12
Total formula weight196661.42
Authors
Luo, J.,Malia, T.J.,Buckley, P.T. (deposition date: 2021-12-15, release date: 2023-01-11, Last modification date: 2024-11-06)
Primary citationBuckley, P.T.,Chan, R.,Fernandez, J.,Luo, J.,Lacey, K.A.,DuMont, A.L.,O'Malley, A.,Brezski, R.J.,Zheng, S.,Malia, T.,Whitaker, B.,Zwolak, A.,Payne, A.,Clark, D.,Sigg, M.,Lacy, E.R.,Kornilova, A.,Kwok, D.,McCarthy, S.,Wu, B.,Morrow, B.,Nemeth-Seay, J.,Petley, T.,Wu, S.,Strohl, W.R.,Lynch, A.S.,Torres, V.J.
Multivalent human antibody-centyrin fusion protein to prevent and treat Staphylococcus aureus infections.
Cell Host Microbe, 31:751-765.e11, 2023
Cited by
PubMed Abstract: Treating and preventing infections by antimicrobial-resistant bacterial pathogens is a worldwide problem. Pathogens such as Staphylococcus aureus produce an array of virulence determinants, making it difficult to identify single targets for the development of vaccines or monoclonal therapies. We described a human-derived anti-S. aureus monoclonal antibody (mAb)-centyrin fusion protein ("mAbtyrin") that simultaneously targets multiple bacterial adhesins, resists proteolysis by bacterial protease GluV8, avoids Fc engagement by S. aureus IgG-binding proteins SpA and Sbi, and neutralizes pore-forming leukocidins via fusion with anti-toxin centyrins, while maintaining Fc- and complement-mediated functions. Compared with the parental mAb, mAbtyrin protected human phagocytes and boosted phagocyte-mediated killing. The mAbtyrin also reduced pathology, reduced bacterial burden, and protected from different types of infections in preclinical animal models. Finally, mAbtyrin synergized with vancomycin, enhancing pathogen clearance in an animal model of bacteremia. Altogether, these data establish the potential of multivalent mAbs for treating and preventing S. aureus diseases.
PubMed: 37098341
DOI: 10.1016/j.chom.2023.04.004
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.9 Å)
Structure validation

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