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用于过氧化氢检测的辣根过氧化物酶与单壁碳纳米管的共价连接

Covalent Attachment of Horseradish Peroxidase to Single-Walled Carbon Nanotubes for Hydrogen Peroxide Detection.

作者信息

Ledesma Francis, Nishitani Shoichi, Cunningham Francis J, Hubbard Joshua D, Yim Dabin, Lui Alison, Chio Linda, Murali Aishwarya, Landry Markita P

出版信息

bioRxiv. 2023 Dec 15:2023.12.14.571773. doi: 10.1101/2023.12.14.571773.

Abstract

Single-walled carbon nanotubes (SWCNTs) are desirable nanoparticles for sensing biological analytes due to their photostability and intrinsic near-infrared fluorescence. Previous strategies for generating SWCNT nanosensors have leveraged nonspecific adsorption of sensing modalities to the hydrophobic SWCNT surface that often require engineering new molecular recognition elements. An attractive alternate strategy is to leverage pre-existing molecular recognition of proteins for analyte specificity, yet attaching proteins to SWCNT for nanosensor generation remains challenging. Towards this end, we introduce a generalizable platform to generate protein-SWCNT-based optical sensors and use this strategy to synthesize a hydrogen peroxide (H O ) nanosensor by covalently attaching horseradish peroxidase (HRP) to the SWCNT surface. We demonstrate a concentration-dependent response to H O , confirm the nanosensor can image H O in real-time, and assess the nanosensor's selectivity for H O against a panel of biologically relevant analytes. Taken together, these results demonstrate successful covalent attachment of enzymes to SWCNTs while preserving both intrinsic SWCNT fluorescence and enzyme function. We anticipate this platform can be adapted to covalently attach other proteins of interest including other enzymes for sensing or antibodies for targeted imaging and cargo delivery.

摘要

单壁碳纳米管(SWCNTs)因其光稳定性和固有的近红外荧光特性,成为检测生物分析物的理想纳米颗粒。以往制备SWCNT纳米传感器的策略是利用传感模式对疏水SWCNT表面的非特异性吸附,这通常需要设计新的分子识别元件。一种有吸引力的替代策略是利用蛋白质对分析物的固有分子识别特性来实现特异性,但将蛋白质连接到SWCNT上以制备纳米传感器仍然具有挑战性。为此,我们引入了一个通用平台来制备基于蛋白质-SWCNT的光学传感器,并利用该策略通过将辣根过氧化物酶(HRP)共价连接到SWCNT表面来合成过氧化氢(H₂O₂)纳米传感器。我们展示了对H₂O₂的浓度依赖性响应,证实该纳米传感器能够实时成像H₂O₂,并评估了该纳米传感器对H₂O₂相对于一系列生物相关分析物的选择性。综上所述,这些结果表明酶已成功共价连接到SWCNT上,同时保留了SWCNT的固有荧光和酶的功能。我们预计该平台可适用于共价连接其他感兴趣的蛋白质,包括用于传感的其他酶或用于靶向成像和货物递送的抗体。

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