Expression and purification of RHC–EGFP fusion protein and its application in hyaluronic acid assay. Issue 3 (16th March 2017)

• Record Type: Journal Article
• Authors: Duan, Ningjun; Lv, Wansheng; Zhu, Lingli; Zheng, Weijuan; Hua, Zichun
• Is Part Of: Preparative biochemistry & biotechnology. Volume 47:Issue 3(2017)
• Page Start: 261
• Page End: 267
• Publication Date: 2017-03-16
• Subjects: HA: hyaluronic acid -- E. coli: Escherichia coli -- ECM: extracellular matrix -- HABP: hyaluronic acid-binding protein -- RHAMM: receptor for hyaluronan-mediated motility -- RHC: C-terminal domain of RHAMM -- EGFP: enhanced green fluorescence protein -- ELISA: enzyme-linked immunosorbent assay -- IPTG: isopropyl-b-D-thiogalactopyranoside -- TET: tetracycline -- SDS-PAGE: sodium dodecylsulfate polyacrylamide gel electrophoresis -- TBS: tris buffered saline -- PBS: phosphate buffered saline -- FBS: fetal bovine serum; Assay -- EGFP -- HA-binding protein -- hyaluronic acid -- RHAMM; Biochemistry -- Technique -- Periodicals; Biotechnology -- Technique -- Periodicals; Biochemistry -- methods -- Periodicals; Biotechnology -- methods -- Periodicals; 660.6
• DOI: 10.1080/10826068.2016.1224243
• Languages: English
• ISSNs: 1082-6068

Abstract

ABSTRACT: Hyaluronan is a widely distributed glycosaminoglycan which has multiple functions. Hyaluronic acid (HA) accumulation has been reported in many human diseases. Understanding the role of hyaluronan and its binding proteins in the pathobiology of disease will facilitate the development of novel therapeutics for many critical diseases. Current techniques described for the analysis of HA are mainly for HA quantification in solutions, not for the direct detection of HA in tissues or on cell surfaces. In our study, a fusion protein, named C-terminal domain of RHAMM–enhanced green fluorescence protein (RHC–EGFP), combined the HA-binding domain, C-terminal of receptor for hyaluronan-mediated motility, with EGFP, a widely used enhanced green fluorescence protein, was expressed and purified from Escherichia coli with high purity. Based on the sensitivity and convenience of fluorescence detection, methods for direct assay of HA in solutions, on cell surface or in tissues were established using RHC–EGFP. The binding specificity was also confirmed by competitive binding experiment and hyaluronidase degradation experiment. Our results provide an alternative choice for the specific and convenient assay of HA in various samples, and maybe helpful for further understanding of the fundamental and comprehensive functions of HA.