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Updated: Jul 29, 2026

Patterning Bioactive Proteins or Peptides on Hydrogel Using Photochemistry for Biological Applications
Published on: September 15, 2017
A universal protein immobilization method to construct responsive photonic hydrogels with enhanced sensing
Fangyuan Zhao1, Guoqin Ma1, Yuqi Zhang2
1School of Instrumentation and Optoelectronic Engineering, School of Space and Environment, Beihang University, Beijing 100191, China.
This study introduces a novel acrylated protein method for developing stable, two-dimensional photonic crystal (PC) hydrogel sensors. These sensors demonstrate high selectivity and stability for detecting hydrogen peroxide and calcium chloride, offering a versatile platform for various applications.
Area of Science:
- Biomaterials Science
- Nanotechnology
- Sensor Technology
Background:
- Photonic crystal (PC) protein hydrogel sensors integrate protein hydrogels with PC platforms, offering advantages for resource-limited settings.
- Existing sensors face limitations in protein diversity and long-term matrix stability.
- Developing robust and versatile protein-based sensors is crucial for advancing diagnostics.
Purpose of the Study:
- To introduce an innovative acrylated protein method for creating stable, two-dimensional (2D) PC hydrogel sensors.
- To demonstrate the versatility of this method using different proteins (horseradish peroxidase and bovine serum albumin) for detecting various analytes.
- To enhance the stability and applicability of PC protein hydrogel sensors.
Main Methods:
- Developed 2D PC hydrogel sensors by immobilizing proteins (HRP and BSA) onto acrylamide hydrogels using an acrylated protein approach.
- Utilized horseradish peroxidase (HRP) immobilized on acrylamide (AAm/HRP) hydrogels for hydrogen peroxide (H₂O₂) detection.
- Employed bovine serum albumin (BSA) immobilized on acrylamide (AAm/BSA) hydrogels for calcium chloride (CaCl₂) detection.
Main Results:
- AAm/HRP hydrogel sensors exhibited high selectivity, chemical stability for at least 14 weeks, and a limit of detection (LoD) of 3.75 μM for H₂O₂.
- AAm/HRP sensors showed distinct structural color changes with varying H₂O₂ concentrations, enabling colorimetric analysis.
- AAm/BSA hydrogel sensors demonstrated a LoD of 0.79 μM for CaCl₂ and stability exceeding 30 days, highlighting the method's universality.
Conclusions:
- The novel acrylated protein method enables the development of stable and versatile 2D PC hydrogel sensors.
- This approach overcomes limitations of protein type and matrix stability in existing PC protein hydrogel sensors.
- The universal method facilitates the creation of diverse sensors for a wide range of targets, with broad application potential.
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