首页> 外文期刊>Journal of Materials Chemistry, B. materials for biology and medicine >Synthesis of gold nanocluster- loaded lysozyme nanoparticles for label- free ratiometric fluorescent pH sensing: applications to enzyme- substrate systems and cellular imaging
【24h】

Synthesis of gold nanocluster- loaded lysozyme nanoparticles for label- free ratiometric fluorescent pH sensing: applications to enzyme- substrate systems and cellular imaging

机译:用于标记的Rablumlistric荧光pH传感的金纳米蛋白含有溶菌酶纳米粒子的合成:应用于酶底物系统和蜂窝成像的应用

获取原文
获取原文并翻译 | 示例
       

摘要

This study developed a simple strategy to prepare lysozyme nanoparticle-encapsulated gold nanoclusters (LysNP-AuNCs) as a dual emission probe for ratiometric sensing of pH variation in enzyme-substrate systems and live cells. The reduction of a gold ion precursor with lysozyme generated lysozyme-stabilized AuNCs (Lys-AuNCs); they were demonstrated to be self-assembled into nano-aggregates during the formation of AuNCs. The aggregated Lys-AuNCs were treated with glutaraldehyde, triggering the conversion of aggregated lysozymes into green-emitting lysozyme nanoparticles (LysNPs) via the formation of C?N bonds. As a result, the AuNCs were well-distributed inside the LysNPs, as demonstrated by transmission electron microscopy and size-exclusion chromatography. The as-prepared LysNP-AuNCs exhibited two separate emission bands, a large Stokes shift, excellent photostability, and salt stability. The pH-induced change in the fluorescence of LysNPs enabled LysNP-AuNCs to ratiometrically detect slight changes (0.2 pH unit) in the pH range from 7.5 to 9.5. Additionally, LysNP-AuNCs were well-suited to probing enzymatic reaction-induced pH changes, which was exemplified by urease-mediated hydrolysis of urea. Under a single excitation, LysNP-AuNCs were used to monitor dual fluorescent images of HeLa cells under different pH conditions.
机译:该研究开发了一种简单的策略,用于制备溶菌酶纳米颗粒包封的金纳米蛋白(LysnP-Aunc)作为酶 - 衬底系统和活细胞的PH变异的足够感测的二元排放探针。用溶菌酶产生的溶菌酶稳定的Aunc(Lys-auncs)还原金离子前体;它们在形成Auncs期间被证明它们被自组装成纳米聚集体。用戊二醛处理聚集的Lys-auncs,通过形成C-N键,将聚集的溶菌酶转化为绿色发射溶菌酶纳米颗粒(Lysnps)。结果,通过透射电子显微镜和尺寸排除色谱法证明,Auncs在Lysnps内部分布得很好。制备的leysnp-auncs表现出两种单独的发射带,大斯托克斯换档,优异的光稳定性和盐稳定性。 Lysnps的Lysnp-auncs的荧光的pH诱导的荧光变化在pH范围为7.5至9.5的pH范围内测定略微检测略微变化(0.2 pH单位)。另外,Lysnp-auncs非常适合于探测酶促反应诱导的pH变化,这是通过脲酶介导的尿素的水解的例子。在一次激发下,使用Lysnp-auncs在不同的pH条件下监测HeLa细胞的双荧光图像。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号