[Purification and characterization of two PR-10 protein isoforms from the crude drug of Angelica sinensis]

Sheng Wu Gong Cheng Xue Bao. 2019 Jan 25;35(1):159-168. doi: 10.13345/j.cjb.180087.
[Article in Chinese]

Abstract

Two proteins of similar molecular weight (named as ASPR-C-1 and ASPR-C-2) from the crude drug of Angelica sinensis were purified and characterized by 80% ammonium sulfate precipitation, Sephadex G-50 gel filtration chromatography, and DEAE-Sepharose anion exchange chromatography. The molecular weight of ASPR-C-1 and ASPR-C-2 on SDS-PAGE was 17.33 kDa and 17.18 kDa, respectively. They were mainly monomeric in solution, but partially formed dimers and they were glycoproteins with glycosyl content of 2.6% and 8.2%, respectively. Both ASPR-C-1 and ASPR-C-2 were identified to be members of pathogenesis-related 10 family of proteins by matrix-assisted laser desorption ionization time-of-flight mass spectrometry and have ribonuclease activities with the specific activity of 73.60 U/mg and 146.76 U/mg, respectively. The optimum pH of the two isoforms was similar, at about 5.6, while their optimum temperatures were different. The optimum temperature of ASPR-C-1 was 50 ℃, and that of ASPR-C-2 was 60 ℃. Both isoforms presented highest thermal stability at 60 ℃. However, ASPR-C-2 was more thermotolerant than ASPR-C-1. The latter was rapidly inactivated and retained only about 20% residual activity while the former still maintained about 80% of its original activity at a higher treatment temperature (80 to 100 ℃). In addition, Fe²⁺ had an activating effect on the ribonuclease activities of two isoforms while Ca²⁺, Mg²⁺, Zn²⁺, Mn²⁺, Ag⁺, Cu²⁺, EDTA (Elhylene diamine tetraacetic acid), dithiothreitol and sodium dodecylsulphate showed different degrees of inhibition of the enzyme activities. Our findings provide a foundation for further research on the biological function of PR-10 protein from Angelica sinensis.

为了进一步研究当归 (Angelica sinensis) 生药中的蛋白质及其功能,通过80%硫酸铵沉淀、Sephadex G-50 凝胶过滤层析、DEAE-Sepharose 阴离子交换层析,首次从当归生药中纯化出两种分子量相近的蛋白 (命名为ASPR-C-1 和ASPR-C-2)。ASPR-C-1 和ASPR-C-2 在SDS-PAGE 上的分子量分别为17.33 kDa 和17.18 kDa,在溶液中主要以单体形式存在,但会部分形成二聚体,二者均为糖蛋白,糖基含量分别为2.6%和8.2%。经基质辅助激光解吸电离飞行时间质谱 (MALDI-TOF-TOF™) 鉴定发现ASPR-C-1 和ASPR-C-2 均为病程相关(Pathogenesis-related 10,PR-10) 家族蛋白,且具有核糖核酸酶活性,比活分别为73.60 U/mg 和146.76 U/mg。两种蛋白的最适pH 相近,均为5.6 左右,但最适温度不同,ASPR-C-1 的为50 ℃,ASPR-C-2 的为60 ℃。二者虽然在60 ℃下都表现出最大的酶活力稳定性,但在更高的处理温度 (80–100 ℃) 下,ASPR-C-1 迅速失活,最终仅余20%左右活力,ASPR-C-2 则表现出良好的热稳定性,最终仍有80%左右活力。此外,Fe²⁺对二者的酶活性具有激活作用,而Ca²⁺、Mg²⁺、Zn²⁺、Mn²⁺、Ag⁺、Cu²⁺、EDTA、DTT 和SDS 则会不同程度地抑制二者的酶活性。研究结果为深入研究来自当归生药的PR-10 蛋白的生物学功能奠定了基础。.

Keywords: PR-10; crude drug of Angelica sinensis; glycoprotein; purify; ribonuclease.

MeSH terms

  • Angelica sinensis*
  • Chromatography, Gel
  • Chromatography, Ion Exchange
  • Electrophoresis, Polyacrylamide Gel
  • Enzyme Stability
  • Hydrogen-Ion Concentration
  • Kinetics
  • Molecular Weight
  • Protein Isoforms
  • Temperature

Substances

  • Protein Isoforms