Accelerating the Peroxidase-Like Activity of Gold Nanoclusters at Neutral pH for Colorimetric Detection of Heparin and Heparinase Activity

• Published in: Analytical chemistry (Washington) 2018-05, Vol.90 (10), p.6247-6252
• Main Authors: Hu, Lianzhe, Liao, Hong, Feng, Lingyan, Wang, Min, Fu, Wensheng
• Format: Article
• Language: English
• Subjects: Anticoagulants; Biological activity; Catalysis; Catalytic activity; Catalytic oxidation; Chemistry; Colorimetry; Deactivation; Gold; Heparin; Hydrogen peroxide; Nanoclusters; Oxidation; Peroxidase; pH effects; Substrates
• ISSN: 0003-2700; 1520-6882
• DOI: 10.1021/acs.analchem.8b00885

The peroxidase-like catalytic activity of gold nanoclusters (Au-NCs) is quite low around physiological pH, which greatly limits their biological applications. Herein, we found heparin can greatly accelerate the peroxidase-like activity of Au-NCs at neutral pH. The catalytic activity of Au-NCs toward the peroxidase substrate 3,3′,5,5′-tetramethylbenzidine (TMB) oxidation by H2O2 was 25-fold increased in the presence of heparin at pH 7. The addition of heparin not only accelerated the initial catalytic rate of Au-NCs but also prevented the Au-NCs from catalyst deactivation. This allows the sensitive colorimetric detection of heparin at neutral pH. In the presence of heparinase, heparin was hydrolyzed into small fragments, weakening the enhancement effect of catalytic activity. On the basis of this phenomenon, the colorimetric determination of heparinase in the range from 0.1 to 3 μg·mL–1 was developed with a detection limit of 0.06 μg·mL–1. Finally, the detection of heparin and heparinase activity in diluted serum samples was also demonstrated.