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Light scattered by model phantom bacteria reveals molecular interactions at their surface

机译:模型幻影细菌散射的光揭示了它们表面的分子相互作用

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摘要

Testing molecular interactions is an ubiquitous need in modern biology and molecular medicine. Here, we present a qualitative and quantitative method rooted in the basic properties of the scattering of light, enabling detailed measurement of ligand-receptor interactions occurring on the surface of colloids. The key factor is the use of receptor-coated nanospheres matched in refractive index with water and therefore optically undetectable ("phantom") when not involved in adhesion processes. At the occurrence of ligand binding at the receptor sites, optically unmatched material adsorbs on the nanoparticle surface, giving rise to an increment in their scattering cross section up to a maximum corresponding to saturated binding sites. The analysis of the scattering growth pattern enables extracting the binding affinity. This label-free method has been assessed through the determination of the binding constant of the antibiotic vancomycin with the tripeptide L-Lys-D-Ala-D-Ala and of the vancomycin dimerization constant. We shed light on the role of chelate effect and molecular hindrance in the activity of this glycopeptide.
机译:在现代生物学和分子医学中,测试分子相互作用是普遍存在的需求。在这里,我们提出了一种定性和定量的方法,该方法植根于光散射的基本特性,可以详细测量胶体表面上发生的配体-受体相互作用。关键因素是使用折射率与水匹配的受体涂层纳米球,因此当不参与粘附过程时,光学上无法检测到(“幻影”​​)。在受体位置发生配体结合时,光学上不匹配的材料吸附在纳米颗粒表面,从而导致其散射截面的增加达到与饱和结合位点对应的最大值。散射生长模式的分析使得能够提取结合亲和力。通过测定抗生素万古霉素与三肽L-Lys-D-Ala-D-Ala的结合常数和万古霉素二聚化常数,评估了这种无标记方法。我们阐明了螯合作用和分子障碍在该糖肽活性中的作用。

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