Real-Time Electrochemical Monitoring of Cellular H2O2 Integrated with In Situ Selective Cultivation of Living Cells Based on Dual Functional Protein Microarrays at Au−TiO2 Surfaces

• Published in: Analytical chemistry (Washington) Vol. 82; no. 15; pp. 6512 - 6518
• Main Authors: Li, Xiaoguang, Liu, Yan, Zhu, Anwei, Luo, Yongping, Deng, Zifeng, Tian, Yang
• Format: Journal Article
• Language: English
• Published: Washington, DC American Chemical Society 01-08-2010
• Subjects: Analytical chemistry; Cell Line, Tumor; Chemistry; Cysteine - chemistry; Cytochromes c - chemistry; Cytochromes c - metabolism; Electrochemical methods; Electrochemical Techniques - methods; Exact sciences and technology; General, instrumentation; Gold - chemistry; Humans; Hydrogen Peroxide - analysis; Protein Array Analysis - methods; Surface Properties; Time Factors; Titanium - chemistry; Performance evaluation; Cell culture; Cysteine; Hydrogen peroxide; Electrochemical method; In situ; Microanalysis; Immobilization; Electron transfer; Selectivity; Enzymatic activity; Detection limit; Heme; Monitoring; Chemical sensor; Real time; Adhesion; Protein; Cytochrome c; Array; Substrate; Sensitivity; Response time; Strategy; Detection; Sensor array
• ISSN: 0003-2700; 1520-6882
• DOI: 10.1021/ac100807c

This paper demonstrates a novel strategy for site-selective cell adhesion and in situ cultivation of living cells, integrated with real-time monitoring of cellular small biomolecules based on dual functional protein microarrays. The protein microarrays have been produced on the superhydrophobic|philic Au−TiO2 micropatterns, through further modification of l-cysteine (Cys) and followed by successive immobilization of a model protein, cytochrome c (cyt c). Experimental results have revealed that the created cyt c microarrays play dual functions: one is employed as a robust substrate for site-selective cell adhesion and in situ cultivation of living cells, because the protein microarrays exhibit high selectivity and bioaffinity toward cells, as well as long biostability under cell culture condition up to 7 days. Meanwhile, the cyt c microarrays can also serve as sensing elements for hydrogen peroxide (H2O2) due to the inherent enzymatic activity of the heme center in cyt c. Direct electron transfer of cyt c has been enhanced at the Cys-modified Au−TiO2 (Au−TiO2/Cys) microarrays, and the electrochemical behavior can be tuned by varying the width and spacing of the microband arrays. Furthermore, cyt c is stably immobilized on the Au−TiO2/Cys microarrays and maintains its enzymatic activity after confined on the microarrays. Thus, the optimized cyt c microarrays show striking analytical performance for H2O2 determination, e.g., high sensitivity and selectivity, broad linear range from 10−9 M to 10−2 M, low detection limit down to 2 nM, and short response time within 5 s. As a result, the excellent analytical properties of the cyt c microarrays, as well as the characteristic of the protein microarrays themselves, including high selectivity, long biostability, and good bioaffinity, opens up a method for selective in situ cultivation of cells integrated with real-time detection of signaling biomolecules such as H2O2 released from living cells, which shows potential for physiological and pathological investigations.