Abstract

A simple and feasible pH meter–based immunoassay is reported for detection of C-reactive protein (CRP) using glucose oxidase (GOD)–conjugated dendrimer loaded with platinum nanozyme. Initially, platinum nanozymes were loaded into the dendrimers through an in situ synthetic method. Then, GOD and monoclonal anti-CRP antibody with a high molar ratio were covalently conjugated onto carboxylated dendrimers via typical carbodiimide coupling. The immunoreaction was carried out with a competitive mode in a CRP-coated microplate. Along with formation of immunocomplex, the added glucose was oxidized into gluconic acid and hydrogen peroxide by GOD, and the latter was further decomposed by platinum nanozyme, thus accelerating chemical reaction in the positive direction. The produced gluconic acid changed the pH of detection solution, which was determined using a handheld pH meter. Under optimum conditions, the pH meter–based immunoassay gave a good signal toward target CRP from 0.01 to 100 ng mL−1. The limit of detection was 5.9 pg mL−1. An intermediate precision ≤ 11.2% was acquired with batch-to-batch identification. No nonspecific adsorption was observed during a series of procedures to detect target CRP, and the cross-reaction against other biomarkers was very low. Importantly, our system gave well-matched results for analysis of human serum samples relative to a referenced ELISA kit.Graphical abstract

Highlights

  • C-reactive protein (CRP), a spherical pentameric protein called acute phase reactants, goes up in response to inflammation

  • For the development of the pH meter–based immunoassay, the successful preparation of CRP-coated microplate and monoclonal rabbit anti-human C-reactive protein antibody (mAb)-PtDEN-glucose oxidase (GOD) should be characterized in detail

  • The pH shift in the presence of target CRP was ascribed to the competitive immunoreaction between target CRP and the coated CRP on the microplate for the labeled mAb on mAb-PtDEN-GOD, decreasing the captured amount of mAb-PtDEN-GOD on the microplate. These results indicated that the pH meter–based immunoassay was feasible for the detection of target CRP on CRP-coated microplate by using mAb-PtDEN-GOD as the signal tag

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Summary

Introduction

C-reactive protein (CRP), a spherical pentameric protein called acute phase reactants, goes up in response to inflammation. It displays several functions associated with host defense to promote agglutination and bacterial capsular swelling, and complement fixation through its calcium-dependent binding to phosphorylcholine [1]. The concentration of CRP in plasma increases greatly during acute phase response to tissue injuries, infections, cancers, and renal and cardiovascular diseases [2]. It is induced by interleukin-1 and interleukin-6. Sensitive and specific detection of CRP would be advantageous for protein diagnostics

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