Munich Center for Integrated Protein Science, CIPS-M, und Lehrstuhl für Biologische Chemie, Technische Universität München, 85354, Freising, Weihenstephan, Germany.
Lehrstuhl für Analytische Chemie, Technische Universität München, 81377, München, Germany.
Angew Chem Int Ed Engl. 2017 Aug 21;56(35):10592-10597. doi: 10.1002/anie.201703893. Epub 2017 Jul 21.
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 (K ≈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.
苯并[a]芘是有机物质不完全燃烧产生的一种丰富的有毒污染物,因为其致癌代谢降解产物。高亲和力(K≈3nm)单克隆抗体 22F12 允许轻松地对苯并[a]芘进行生物分析定量,即使在复杂基质中也是如此。我们报告了 V 基因克隆和作为重组 Fab 片段生产后,22F12 与 3-羟基苯并[a]芘复合物的功能和 X 射线晶体学分析。多环芳烃结合在轻链和重链之间的深口袋中,主要由芳香族和脂肪族氨基酸侧链包围。有趣的是,半抗原-抗体界面的密度低于预期,并且与多环芳烃π-电子系统呈现出极性、氢键样相互作用,这可能允许抗体在水相环境中保持大的、主要是疏水的结合位点,同时为其配体提供足够的互补性。