Renzi Emilia, Esposito Alessandra, Leone Linda, Chávez Miriam, Pineda Teresa, Lombardi Angela, Nastri Flavia
Department of Chemical Sciences, University of Naples Federico II, Complesso Universitario Monte S. Angelo via Cintia Naples 80126 Italy
Department of Physical Chemistry and Applied Thermodynamics, Institute of Chemistry for Energy and Environment, University of Cordoba, Campus Rabanales Ed. Marie Curie Córdoba E-14014 Spain.
Nanoscale Adv. 2024 Jun 3;6(14):3533-3542. doi: 10.1039/d4na00344f. eCollection 2024 Jul 9.
The immobilization of biocatalysts on inorganic supports allows the development of bio-nanohybrid materials with defined functional properties. Gold nanomaterials (AuNMs) are the main players in this field, due to their fascinating shape-dependent properties that account for their versatility. Even though incredible progress has been made in the preparation of AuNMs, few studies have been carried out to analyze the impact of particle morphology on the behavior of immobilized biocatalysts. Herein, the artificial peroxidase Fe(iii)-Mimochrome VIa (FeMC6a) was conjugated to two different anisotropic gold nanomaterials, nanorods (AuNRs) and triangular nanoprisms (AuNTs), to investigate how the properties of the nanosupport can affect the functional behavior of FeMC6a. The conjugation of FeMC6a to AuNMs was performed by a click-chemistry approach, using FeMC6a modified with pegylated aza-dibenzocyclooctyne (FeMC6a-PEG@DBCO), which was allowed to react with azide-functionalized AuNRs and AuNTs, synthesized from citrate-capped AuNMs. To this end, a literature protocol for depleting CTAB from AuNRs was herein reported for the first time to prepare citrate-AuNTs. The overall results suggest that the nanomaterial shape influences the nanoconjugate functional properties. Besides giving new insights into the effect of the surfaces on the artificial peroxidase properties, these results open up the way for creating novel nanostructures with potential applications in the field of sensing devices.
将生物催化剂固定在无机载体上能够开发出具有特定功能特性的生物纳米杂化材料。金纳米材料(AuNMs)是该领域的主要参与者,这归因于其迷人的形状依赖性特性,正是这些特性使其具有多功能性。尽管在AuNMs的制备方面已经取得了令人难以置信的进展,但很少有研究分析颗粒形态对固定化生物催化剂行为的影响。在此,将人工过氧化物酶Fe(iii)-Mimochrome VIa(FeMC6a)与两种不同的各向异性金纳米材料,即纳米棒(AuNRs)和三角形纳米棱镜(AuNTs)进行共轭,以研究纳米载体的性质如何影响FeMC6a的功能行为。FeMC6a与AuNMs的共轭通过点击化学方法进行,使用经聚乙二醇化氮杂二苯并环辛炔修饰的FeMC6a(FeMC6a-PEG@DBCO),使其与由柠檬酸盐封端的AuNMs合成的叠氮化物功能化的AuNRs和AuNTs反应。为此,本文首次报道了一种从AuNRs中去除十六烷基三甲基溴化铵(CTAB)以制备柠檬酸盐-AuNTs的文献方法。总体结果表明,纳米材料的形状会影响纳米共轭物的功能特性。这些结果除了为表面对人工过氧化物酶性质的影响提供新的见解外,还为创建在传感设备领域具有潜在应用的新型纳米结构开辟了道路。