2WRZ

Crystal structure of an arabinose binding protein with designed serotonin binding site in open, ligand-free state

2WRZ の概要

• エントリーDOI: 10.2210/pdb2wrz/pdb
• 関連するPDBエントリー: 1ABE 1ABF 1APB 1BAP 5ABP 6ABP 7ABP 8ABP 9ABP
• 分子名称: L-ARABINOSE-BINDING PERIPLASMIC PROTEIN (2 entities in total)
• 機能のキーワード: sugar transport, arabinose binding protein, periplasmic binding protein, abp, transport protein, periplasm, receptor design
• 由来する生物種: ESCHERICHIA COLI
• 細胞内の位置: Periplasm: P02924
• タンパク質・核酸の鎖数: 2
• 化学式量合計: 66005.09

構造登録者

Schreier, B.,Stumpp, C.,Wiesner, S.,Hocker, B. (登録日: 2009-09-03, 公開日: 2009-10-13, 最終更新日: 2023-12-20)

主引用文献

Schreier, B.,Stumpp, C.,Wiesner, S.,Hocker, B.
The Computational Design of Ligand Binding is not a Solved Problem
Proc.Natl.Acad.Sci.USA, 106:18491-, 2009

PubMed Abstract: Computational design has been very successful in recent years: multiple novel ligand binding proteins as well as enzymes have been reported. We wanted to know in molecular detail how precise the predictions of the interactions of protein and ligands are. Therefore, we performed a structural analysis of a number of published receptors designed onto the periplasmic binding protein scaffold that were reported to bind to the new ligands with nano- to micromolar affinities. It turned out that most of these designed proteins are not suitable for structural studies due to instability and aggregation. However, we were able to solve the crystal structure of an arabinose binding protein designed to bind serotonin to 2.2 A resolution. While crystallized in the presence of an excess of serotonin, the protein is in an open conformation with no serotonin bound, although the side-chain conformations in the empty binding pocket are very similar to the conformations predicted. During subsequent characterization using isothermal titration calorimetry, CD, and NMR spectroscopy, no indication of binding could be detected for any of the tested designed receptors, whereas wild-type proteins bound their ligands as expected. We conclude that although the computational prediction of side-chain conformations appears to be working, it does not necessarily confer binding as expected. Hence, the computational design of ligand binding is not a solved problem and needs to be revisited.

PubMed: 19833875
DOI: 10.1073/PNAS.0907950106

実験手法

X-RAY DIFFRACTION (2.2 Å)