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Size-dependent tuning of horseradish peroxidase bioreactivity by gold nanoparticles

机译:辣根过氧化物酶的尺度依赖的调优bioreactivity的金纳米粒子

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Molecules with diverse biological functions, such as heme peroxidases, can be useful tools for identifying potential biological effects of gold nanoparticles (AuNPs) at the molecular level. Here, using UV-Vis, circular dichroism, dynamic light scattering, and electron spin resonance spectroscopy, we report tuning of horseradish peroxidase (HRP) bioactivity by reactant-free AuNPs with diameters of 5, 10, 15, 30 and 60 nm (Au-5 nm, Au-10 nm, Au-15 nm, Au-30 nm and Au-60 nm). HRP conjugation to AuNPs was observed with only Au-5 nm and Au-10 nm prominently increasing the a-helicity of the enzyme to extents inversely related to their size. Au-5 nm inhibited both HRP peroxidase activity toward 3,3',5,5'-tetramethylbenzidine and HRP compound I/II reactivity toward 5,5-dimethyl-1-pyrroline N-oxide. Au-5 nm enhanced the HRP peroxidase activity toward ascorbic acid and the HRP compound I/II reactivity toward redox-active residues in the HRP protein moiety. Further, Au-5 nm also decreased the catalase-and oxidase-like activities of HRP. Au-10 nm showed similar, but weaker effects, while Au-15 nm, Au-30 nm and Au-60 nm had no effect. Results suggest that AuNPs can size-dependently enhance or inhibit HRP bioreactivity toward substrates with different redox potentials via a mechanism involving extension of the HRP substrate access channel and decline in the redox potentials of HRP catalytic intermediates.
机译:等多种生物功能分子血红素氧化酵素,可以有用的工具识别潜在的生物效应的黄金纳米颗粒(AuNPs)在分子水平上。在这里,使用紫外可见、圆二色性、动态光散射和电子自旋共振光谱,我们报告调优的辣根过氧化物酶(合)由reactant-free生物活性AuNPs直径在5、10、15、30、60 nm(Au-5 Au-10 nm, Au-15纳米之间,and Au-60 Au-30 nm海里)。只有Au-5 nm和Au-10 nm显著增加酶的a-helicity区段反向它们的大小有关。过氧化物酶活性对3, 3, 5, 5 ' -tetramethylbenzidine合化合物对5 I / II反应,5-dimethyl-1-pyrrolineN-oxide。活动向抗坏血酸和合对redox-active化合物I / II反应残留在合蛋白质的一部分。海里也降低了catalase-and oxidase-like合活动。较弱的影响,而Au-15 nm, Au-30 nmAu-60海里没有效果。AuNPs可以size-dependently增强或抑制合bioreactivity基质不同通过一个机制涉及氧化还原电位合底物的扩展通道和访问合催化氧化还原电位的下降中间体。

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