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Tight Molecular Recognition of Benzo[a]pyrene by a High-Affinity Antibody.
Eichinger, Andreas; Neumaier, Irmgard; Pschenitza, Michael; Niessner, Reinhard; Knopp, Dietmar; Skerra, Arne.
Afiliação
  • Eichinger A; Munich Center for Integrated Protein Science, CIPS-M, und Lehrstuhl für Biologische Chemie, Technische Universität München, 85354, Freising, Weihenstephan, Germany.
  • Neumaier I; Munich Center for Integrated Protein Science, CIPS-M, und Lehrstuhl für Biologische Chemie, Technische Universität München, 85354, Freising, Weihenstephan, Germany.
  • Pschenitza M; Lehrstuhl für Analytische Chemie, Technische Universität München, 81377, München, Germany.
  • Niessner R; Lehrstuhl für Analytische Chemie, Technische Universität München, 81377, München, Germany.
  • Knopp D; Lehrstuhl für Analytische Chemie, Technische Universität München, 81377, München, Germany.
  • Skerra A; Munich Center for Integrated Protein Science, CIPS-M, und Lehrstuhl für Biologische Chemie, Technische Universität München, 85354, Freising, Weihenstephan, Germany.
Angew Chem Int Ed Engl ; 56(35): 10592-10597, 2017 08 21.
Article em En | MEDLINE | ID: mdl-28603847
Benzo[a]pyrene, which is produced during the incomplete combustion of organic material, is an abundant noxious pollutant because of its carcinogenic metabolic degradation products. The high-affinity (KD ≈3 nm) monoclonal antibody 22F12 allows facile bioanalytical quantification of benzo[a]pyrene even in complex matrices. We report the functional and X-ray crystallographic analysis of 22F12 in complex with 3-hydroxybenzo[a]pyrene after cloning of the V-genes and production as a recombinant Fab fragment. The polycyclic aromatic hydrocarbon is bound in a deep pocket between the light and heavy chains, surrounded mainly by aromatic and aliphatic amino acid side chains. Interestingly, the hapten-antibody interface is less densely packed than expected and reveals polar, H-bond-like interactions with the polycyclic aromatic π-electron system, which may allow the antibody to maintain a large, predominantly hydrophobic binding site in an aqueous environment while providing sufficient complementarity to its ligand.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Benzo(a)pireno / Anticorpos Monoclonais Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Benzo(a)pireno / Anticorpos Monoclonais Idioma: En Ano de publicação: 2017 Tipo de documento: Article