Resorc[4]arene Modifiers for Supramolecular Site‐Directed Immobilization of Antibodies on Multi‐Walled Carbon Nanotubes

Author:

Polli Francesca1ORCID,Cianfoni Gabriele12ORCID,Elnahas Rem3ORCID,Mangiardi Laura12,Scaramuzzo Francesca A.4ORCID,Cammarone Silvia1ORCID,Quaglio Deborah1ORCID,Calcaterra Andrea1ORCID,Pierini Marco1ORCID,Mazzei Franco1ORCID,Zanoni Robertino3ORCID,Botta Bruno1ORCID,Ghirga Francesca1ORCID

Affiliation:

1. Department of Chemistry and Technology of Drugs Department of Excellence 2018–2022 Sapienza-University of Rome, P.le Aldo Moro 5 00185 Rome Italy

2. Center for Life Nano- and Neuro-Science@Sapienza Italian Institute of Technology Viale Regina Elena 291 00161 Rome Italy

3. Department of Chemistry Sapienza-University of Rome P.le Aldo Moro 5 00185 Rome Italy

4. Department of Basic and Applied Sciences for Engineering Sapienza - University of Rome Via del Castro Laurenziano 7 00161 Rome Italy

Abstract

AbstractOne of the main problems in developing immunosensors featuring carbon nanotubes (CNTs) is immobilizing antibodies (Abs) onto the CNT surface to afford selective binding to target antigens (Ags). In this work, we developed a practical supramolecular Ab conjugation strategy based on resorc[4]arene modifiers. To improve the Ab orientation on the CNTs surface and optimizing the Ab/Ag interaction, we exploited the host‐guest approach by synthesizing two newly resorc[4]arene linkers R1 and R2 via well‐established procedures. The upper rim was decorated with eight methoxyl groups to promote selective recognition of the fragment crystallizable (Fc) region of the Ab. Moreover, the lower rim was functionalized with 3‐bromopropyloxy or 3‐azidopropiloxy substituents to bind the macrocycles on the multi‐walled carbon nanotubes (MWCNTs) surface. Accordingly, several chemical modifications of MWCNTs were evaluated. After the morphological and electrochemical characterization of nanomaterials, the resorc[4]arene‐modified MWCNTs were deposited onto a glassy carbon electrode surface to evaluate their potential applicability for label‐free immunosensor development. The most promising system showed an improved electrode active area (AEL) of almost 20 % and a site‐oriented immobilization of the SARS‐CoV‐2 spike protein S1 antibody (Ab‐SPS1). The developed immunosensor revealed a good sensitivity (23.64 μA mL ng−1 cm−2) towards the SPS1 antigen and a limit of detection (LOD) of 1.01 ng mL−1.

Publisher

Wiley

Subject

Organic Chemistry,Molecular Biology,Molecular Medicine,Biochemistry

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