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Controlled Immobilization Strategies to Probe Short Hyaluronan-Protein Interactions

机译:控制固定策略探讨短透明质蛋白蛋白质相互作用

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Well-controlled grafting of small hyaluronan oligosaccharides (sHA) enables novel approaches to investigate biological processes such as angiogenesis, immune reactions and cancer metastasis. We develop two strategies for covalent attachment of sHA, a fast high-density adsorption and a two-layer system that allows tuning the density and mode of immobilization. We monitored the sHA adlayer formation and subsequent macromolecular interactions by label-free quartz crystal microbalance with dissipation (QCM-D). The modified surfaces are inert to unspecific protein adsorption, and yet retain the specific binding capacity of sHA. Thus they are an ideal tool to study the interactions of hyaluronan-binding proteins and short hyaluronan molecules as demonstrated by the specific recognition of LYVE-1 and aggrecan. Both hyaladherins recognize sHA and the binding is independent to the presence of the reducing end.
机译:良好的透明质寡糖(SHA)的良好嫁接使新的方法能够研究生物学过程,例如血管生成,免疫反应和癌症转移。我们开发了SHA的共价附着的两种策略,一种快速的高密度吸附和双层系统,允许调节固定的密度和模式。我们通过用耗散(QCM-D)的无标记石英晶体微稳定监测SHA adlayer形成和随后的大分子相互作用。改性表面对未特异性的蛋白质吸附呈惰性,但还保持了SHA的特异性结合能力。因此,它们是研究透明质酸结合蛋白和短透明质酸分子的相互作用的理想工具,如Lyve-1和骨料的具体识别所证明的那样。透明质素识别出SHA,结合是独立于还原端的存在。

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