Clarke Teresa E, Braun Volkmar, Winkelmann Gunther, Tari Leslie W, Vogel Hans J
Structural Biology Research Group, Department of Biological Sciences, University of Calgary, 2500 University Dr. N.W., Calgary, Alberta T2N 1N4, Canada.
J Biol Chem. 2002 Apr 19;277(16):13966-72. doi: 10.1074/jbc.M109385200. Epub 2002 Jan 22.
Siderophore-binding proteins play an essential role in the uptake of iron in many Gram-positive and Gram-negative bacteria. FhuD is an ATP-binding cassette-type (ABC-type) binding protein involved in the uptake of hydroxamate-type siderophores in Escherichia coli. Structures of FhuD complexed with the antibiotic albomycin, the fungal siderophore coprogen and the drug Desferal have been determined at high resolution by x-ray crystallography. FhuD has an unusual bilobal structure for a periplasmic ligand binding protein, with two mixed beta/alpha domains connected by a long alpha-helix. The binding site for hydroxamate-type ligands is composed of a shallow pocket that lies between these two domains. Recognition of siderophores primarily occurs through interactions between the iron-hydroxamate centers of each siderophore and the side chains of several key residues in the binding pocket. Rearrangements of side chains within the binding pocket accommodate the unique structural features of each siderophore. The backbones of the siderophores are not involved in any direct interactions with the protein, demonstrating how siderophores with considerable chemical and structural diversity can be bound by FhuD. For albomycin, which consists of an antibiotic group attached to a hydroxamate siderophore, electron density for the antibiotic portion was not observed. Therefore, this study provides a basis for the rational design of novel bacteriostatic agents, in the form of siderophore-antibiotic conjugates that can act as "Trojan horses," using the hydroxamate-type siderophore uptake system to actively deliver antibiotics directly into targeted pathogens.
铁载体结合蛋白在许多革兰氏阳性和革兰氏阴性细菌摄取铁的过程中发挥着至关重要的作用。FhuD是一种ATP结合盒式(ABC型)结合蛋白,参与大肠杆菌中异羟肟酸型铁载体的摄取。通过X射线晶体学已高分辨率测定了与抗生素白霉素、真菌铁载体粪卟啉和药物去铁胺复合的FhuD的结构。FhuD对于周质配体结合蛋白具有不寻常的双叶结构,有两个由长α螺旋连接的混合β/α结构域。异羟肟酸型配体的结合位点由位于这两个结构域之间的浅口袋组成。铁载体的识别主要通过每个铁载体的铁-异羟肟酸中心与结合口袋中几个关键残基的侧链之间的相互作用发生。结合口袋内侧链的重排适应了每个铁载体的独特结构特征。铁载体的主链不与蛋白质发生任何直接相互作用,这表明具有相当化学和结构多样性的铁载体如何能够被FhuD结合。对于由连接到异羟肟酸铁载体上的抗生素基团组成的白霉素,未观察到抗生素部分的电子密度。因此,本研究为合理设计新型抑菌剂提供了基础,其形式为铁载体-抗生素缀合物,可作为“特洛伊木马”,利用异羟肟酸型铁载体摄取系统将抗生素直接主动递送至靶向病原体中。