TY - JOUR
T1 - Tight Molecular Recognition of Benzo[a]pyrene by a High-Affinity Antibody
AU - Eichinger, Andreas
AU - Neumaier, Irmgard
AU - Pschenitza, Michael
AU - Niessner, Reinhard
AU - Knopp, Dietmar
AU - Skerra, Arne
N1 - Publisher Copyright:
© 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim
PY - 2017/8/21
Y1 - 2017/8/21
N2 - 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.
AB - 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.
KW - X-ray crystallography
KW - antibodies
KW - benzo[a]pyrenes
KW - molecular recognition
KW - polycyclic aromatic hydrocarbons
UR - http://www.scopus.com/inward/record.url?scp=85025456755&partnerID=8YFLogxK
U2 - 10.1002/anie.201703893
DO - 10.1002/anie.201703893
M3 - Article
C2 - 28603847
AN - SCOPUS:85025456755
SN - 1433-7851
VL - 56
SP - 10592
EP - 10597
JO - Angewandte Chemie International Edition in English
JF - Angewandte Chemie International Edition in English
IS - 35
ER -