Protecting Peroxidase Activity of Multilayer Enzyme-Polyion Films Using Outer Catalase Layers

• Published in: The journal of physical chemistry. B Vol. 111; no. 51; pp. 14378 - 14386
• Main Authors: Lu, Haiyun, Rusling, James F, Hu, Naifei
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 27-12-2007
• Subjects: Biosensing Techniques - methods; Catalase - chemistry; Catalase - metabolism; Catalysis; Electrochemistry; Electrolytes - chemistry; Enzymes, Immobilized - chemistry; Enzymes, Immobilized - metabolism; Horseradish Peroxidase - chemistry; Horseradish Peroxidase - metabolism; Hyaluronic Acid - chemistry; Hyaluronic Acid - metabolism; Hydrogen Peroxide - chemistry; Myoglobin - chemistry; Myoglobin - metabolism; Oxidation-Reduction; Sensitivity and Specificity; Surface Properties
• ISSN: 1520-6106; 1520-5207
• DOI: 10.1021/jp076036w

Films constructed layer-by-layer on electrodes with architecture {protein/hyaluronic acid (HA)} n containing myoglobin (Mb) or horseradish peroxidase (HRP) were protected against protein damage by H2O2 by using outer catalase layers. Peroxidase activity for substrate oxidation requires activation by H2O2, but {protein/HA} n films without outer catalase layers are damaged slowly and irreversibly by H2O2. The rate and extent of damage were decreased dramatically by adding outer catalase layers to decompose H2O2. Comparative studies suggest that protection results from catalase decomposing a fraction of the H2O2 as it enters the film, rather than by an in-film diffusion barrier. The outer catalase layers controlled the rate of H2O2 entry into inner regions of the film, and they biased the system to favor electrocatalytic peroxide reduction over enzyme damage. Catalase-protected {protein/HA} n films had an increased linear concentration range for H2O2 detection. This approach offers an effective way to protect biosensors from damage by H2O2.