Pathogen Inhibition by Multivalent Ligand Architectures

被引:153
作者
Bhatia, Sumati [1 ]
Camacho, Luis Cuellar [1 ]
Haag, Rainer [1 ]
机构
[1] Free Univ Berlin, Inst Chem & Biochem, Takustr 3, D-14195 Berlin, Germany
关键词
SURFACE-PLASMON RESONANCE; ISOTHERMAL TITRATION CALORIMETRY; INFLUENZA-A VIRUS; RECEPTOR-BINDING; PSEUDOMONAS-AERUGINOSA; BIOMOLECULAR INTERACTIONS; MOLECULAR RECOGNITION; MECHANICAL-PROPERTIES; ELECTRON-MICROSCOPY; FORCE SPECTROSCOPY;
D O I
10.1021/jacs.5b12950
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Interfacial multivalent interactions at pathogen-cell interfaces can be competitively inhibited by multivalent scaffolds that prevent pathogen adhesion to the cells during the initial stages of infection. The lack of understanding of complex biological systems makes the design of an efficient multivalent inhibitor a toilsome task. Therefore, we have highlighted the main issues and concerns associated with blocking pathogen at interfaces, which are dependent on the nature and properties of both multivalent inhibitors and pathogens, such as viruses and bacteria. The challenges associated with different cores or carrier scaffolds of multivalent inhibitors are concisely discussed with selected examples.
引用
收藏
页码:8654 / 8666
页数:13
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