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Bionanoconjugates of tyrosinase and peptide-derivatised gold nanoparticles for biosensing of phenolic compounds

机译:酪氨酸酶和肽衍生的金纳米粒子的生物结合物对酚类化合物的生物传感

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摘要

Bionanoconjugates of the enzyme tyrosinase (TYR) and gold nanoparticles (AuNPs) functionalised with a peptide (CALNN) were produced in solution and characterised. The formation of stable TYR-AuNP:CALNN bionanoconjugates (BNCs) was supported by a decrease of the surface charge of the BNCs as determined by zeta-potential and an increase in hydrodynamic diameter as determined by Dynamic Light Scattering (DLS). UV/Vis studies of pH-induced aggregation revealed distinct protonation patterns for the BNCs when compared with AuNP:CALNN alone, further substantiating BNC formation. Activity studies of the BNCs for the reduction of di-phenols in solution indicated that TYR not only remains active after conjugation, but interestingly its activity in the BNCs is higher than for the free enzyme. In conclusion, AuNP:CALNN can provide a suitable platform for the immobilisation of TYR, leading to BNCs with increased enzyme activity and a wider pH working range, with promising uses in electrochemical biosensors for the detection of mono- and di-phenolic compounds.
机译:在溶液中生成了酪氨酸酶(TYR)和被肽(CALNN)官能化的金纳米颗粒(AuNPs)的Bionanoconjugates。稳定的TYR-AuNP:CALNN生物纳米共轭物(BNCs)的形成受到zeta电位确定的BNCs表面电荷减少和动态光散射(DLS)确定的流体动力学直径增加的支持。与pH诱导的聚集体的UV / Vis研究表明,与单独使用AuNP:CALNN相比,BNC的质子化模式不同,进一步证实了BNC的形成。 BNC对溶液中二酚还原的活性研究表明,TYR不仅在结合后仍保持活性,而且有趣的是,其在BNC中的活性高于游离酶。总之,AuNP:CALNN可以为TYR固定化提供合适的平台,从而使BNC具有更高的酶活性和更宽的pH工作范围,并有望在电化学生物传感器中用于检测单酚和双酚化合物。

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