5CP3

Crystal Structure of an Antigen-Binding Fragment of Monoclonal Antibody against Sulfonamides in Complex with Sulfathiazole

5CP3 の概要

• エントリーDOI: 10.2210/pdb5cp3/pdb
• 関連するPDBエントリー: 5CP7
• 分子名称: Light Chain of Antigen-Binding Fragment of Monoclonal Antibody of 4C7, Heavy Chain of Antigen-Binding Fragment of Monoclonal Antibody of 4C7, 4-amino-N-(1,3-thiazol-2-yl)benzenesulfonamide, ... (6 entities in total)
• 機能のキーワード: sulfathiazole, anti-sulfonamides antibody, antigen-binding fragment, complex, immune system
• 由来する生物種: Mus musculus (Mouse); 詳細
• タンパク質・核酸の鎖数: 2
• 化学式量合計: 47356.70

構造登録者

Wang, Z.,Shen, J.,Li, C.,Li, Y.,Wen, K.,Yu, X.,Zhang, X. (登録日: 2015-07-21, 公開日: 2015-08-05, 最終更新日: 2024-10-23)

主引用文献

Li, C.,Liang, X.,Wen, K.,Li, Y.,Zhang, X.,Ma, M.,Yu, X.,Yu, W.,Shen, J.,Wang, Z.
Class-specific Monoclonal Antibodies and Dihydropteroate Synthase in Bioassays used for the Detection of Sulfonamides: Structural Insights into Recognition Diversity.
Anal. Chem., 91:2392-2400, 2019

PubMed Abstract: Molecular recognition between a receptor and ligand is a fundamental event in bioanalytical assays, which guarantees the sensitivity and specificity of an assay for the detection of the target of interest. An intensive understanding of the interaction mechanism could be useful for desirable hapten design, directed antibody evolution in vitro, and assay improvement. To illustrate the structural information on class-specific monoclonal antibodies (mAbs) and dihydropteroate synthase (DHPS) against sulfonamides (SAs) we have previously prepared, we initially measured the kinetic parameters of mAb 4C7, 4D11, and DHPS, which showed that the affinities of 4C7 and 4D11 were in the pM to μM range, while DHPS was uniformly in the μM range. Three-dimensional quantitative structure-activity relationship analysis for 4C7 and 4D11 then revealed that the contributions from the stereochemical structure and electron density of the SAs were comparable to binding with mAb. To acquire insights into the structural basis of mAbs and DHPS during the recognition process, the crystal structures of 4C7 and its complex with sulfathiazole were determined using X-ray crystallography. The results showed the SAs orientation and hydrogen bonding interactions mainly contributed to the diverse SAs-mAb affinities. However, for DHPS, a nucleophilic substitution reaction occurred during the recognition process with the SAs, which contributed to the surprisingly uniform affinity for all the SAs tested. This study verified the previous hypotheses on antibody production against SAs and enhanced our understanding of antibody-SAs interactions, which provided useful information toward the rational design of novel haptens and directed evolution to produce class-specific antibodies as DHPS.

PubMed: 30580515
DOI: 10.1021/acs.analchem.8b05174

実験手法

X-RAY DIFFRACTION (1.99 Å)