Interaction between heparin and fibronectin: Using quartz crystal microbalance with dissipation, immunochemistry and isothermal titration calorimetry

被引:0
作者
Guicai Li
Caiping Wang
Ping Yang
Jie Zhou
Pingchuan Zhu
机构
[1] Nantong University,Jiangsu Key Laboratory of Neuroregeneration
[2] Southwest Jiaotong University,Key Laboratory for Advanced Technologies of Materials, Ministry of Education
[3] Guangxi University,Guangxi Key Laboratory for Subtropical Bio
来源
Journal of Wuhan University of Technology-Mater. Sci. Ed. | 2015年 / 30卷
关键词
Heparin; fibronectin; QCM-D; immunochemistry; isothermal titration calorimetry;
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摘要
The adsorption behavior of heparin and fibronectin was studied by quartz crystal microbalance with dissipation (QCM-D), and the interaction between heparin and fibronectin was evaluated using immunochemistry and isothermal titration calorimetry (ITC) measurement. The results showed that there was competitive adsorption between heparin and fibronectin, and the preadsorption of fibronectin could prevent subsequent heparin adsorption to some extent, and the adsorbed Hep/Fn complex on the surface was in a rigid form. The bioactivity of heparin and fibronectin could be affected by the bulk concentration of each, and both heparin and fibronectin in Hep/Fn complex formed under pH 4 condition displayed larger bioactivity than that formed under pH 7 condition. Moreover, the fibronectin showed more exposed cell-binding sites at the pH value lower than physiological condition. The results of ITC further suggested that the interaction between heparin and fibronectin under pH 4 was stronger than under pH 7, and the complex was also more stable. The study brings forth the detailed interaction between heparin and fibronectin, which will be helpful for better understanding the interaction mechanism of the two biomolecules. The results may be potentially useful for the development of new generation of cardiovascular biomaterials.
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页码:1074 / 1084
页数:10
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  • [1] Dai J(2004)Structure and Protein Design of a Human Platelet Function Inhibitor[J] Cell 116 649-659
  • [2] Liu J(2010)The Creation of an Antithrombotic Surface by Apyrase Immobilization[J] Biomaterials 31 4484-4491
  • [3] Deng Y(2010)Heparin-Immobilized Polymers as Non-Inflammatory and Non-Thrombogenic Coating Materials for Arsenic Trioxide Eluting Stents[J] Acta Biomater. 6 534-546
  • [4] Nilsson P H(2011)Cell Affinity for bFGF Immobilized Heparin-Containing Poly(lactide-co-glycolide) Scaffolds[J] Biomaterials 32 3404-3412
  • [5] Engberg A E(2006)Effect of Biomaterial Surface Properties on Fibronectin-Alpha5beta1 Integrin Interaction and Cellular Attachment[J] Biomaterials 27 1907-1916
  • [6] Back J(2009)Covalent Immobilisation of Tropoelastin on a Plasma Deposited Interface for Enhancement of Endothelialisation on Metal Srfaces[J] Biomaterials 30 1675-1681
  • [7] Gong F(2003)RGD Modified Polymers: Biomaterials for Stimulated Cell Adhesion and Beyond[J] Biomaterials 24 4385-4415
  • [8] Cheng X(2009)Regulation of Polyurethane Hemocompatibility and Endothelialization by Tethered Hyaluronic Acid Oligosaccharides[J] Biomaterials 30 5341-5351
  • [9] Wang S(1980)Heparin Enhances the Rate of Binding of Fibronectin to Collagen[J] Biochem. J. 187 521-524
  • [10] Shen H(2011)The Effect of Coimmobilizing Heparin and Fibronectinon Titaniumon Hemo compatibility and Endothelialization[J] Biomaterials 32 4691-4703