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木瓜蛋白酶处理的壳聚糖的磺化及其抗凝活性机制。

Sulfonation of papain-treated chitosan and its mechanism for anticoagulant activity.

作者信息

Suwan Jiraporn, Zhang Zhenqing, Li Boyangzi, Vongchan Preeyanat, Meepowpan Puttinan, Zhang Fuming, Mousa Shaker A, Mousa Shaymaa, Premanode Bhusana, Kongtawelert Prachya, Linhardt Robert J

机构信息

Thailand Excellence Center for Tissue Engineering, Department of Biochemistry, Faculty of Medicine, Chiang Mai University, Chiang Mai 50200, Thailand.

出版信息

Carbohydr Res. 2009 Jul 6;344(10):1190-6. doi: 10.1016/j.carres.2009.04.016. Epub 2009 Apr 20.


DOI:10.1016/j.carres.2009.04.016
PMID:19476923
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2727590/
Abstract

The novel low-molecular-weight chitosan polysulfate (MW 5120-26,200 Da) was prepared using the depolymerization of chitosan with papain (EC. 3.4.22.2). The sulfonation of depolymerized products was performed using chlorosulfonic acid in N,N-dimethylformamide under semi-heterogeneous conditions. The structures of the products were characterized by FTIR, (13)C NMR, and (1)H NMR (1D, 2D NMR) spectroscopy. The present study sheds light on the mechanism of anticoagulant activity of chitosan polysulfate. Anticoagulant activity was investigated by an activated partial thromboplastin assay, a thrombin time assay, a prothrombin time assay, and thrombelastography. Surface plasmon resonance also provided valuable data for understanding the relationship between the molecular binding of sulfated chitosan to two important blood clotting regulators, antithrombin III and heparin cofactor II. These results show that the principal mechanism by which this chitosan polysulfate exhibits anticoagulant activity is mediated through heparin cofactor II and is dependent on polysaccharide molecular weight.

摘要

采用木瓜蛋白酶(EC. 3.4.22.2)对壳聚糖进行解聚,制备了新型低分子量壳聚糖多硫酸盐(分子量5120 - 26,200 Da)。在半均相条件下,使用氯磺酸在N,N - 二甲基甲酰胺中对解聚产物进行磺化。通过傅里叶变换红外光谱(FTIR)、碳-13核磁共振(¹³C NMR)和氢-1核磁共振(¹H NMR,一维、二维核磁共振)光谱对产物结构进行表征。本研究揭示了壳聚糖多硫酸盐抗凝活性的机制。通过活化部分凝血活酶时间测定、凝血酶时间测定、凝血酶原时间测定和血栓弹力图研究抗凝活性。表面等离子体共振也为理解硫酸化壳聚糖与两种重要凝血调节因子抗凝血酶III和肝素辅因子II的分子结合之间的关系提供了有价值的数据。这些结果表明,这种壳聚糖多硫酸盐表现出抗凝活性的主要机制是通过肝素辅因子II介导的,并且取决于多糖的分子量。

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本文引用的文献

[1]
Oversulfated chondroitin sulfate is a contaminant in heparin associated with adverse clinical events.

Nat Biotechnol. 2008-6

[2]
Contaminated heparin associated with adverse clinical events and activation of the contact system.

N Engl J Med. 2008-6-5

[3]
Use of a sulfated chitosan derivative to reduce bladder inflammation in the rat.

Urology. 2007-11

[4]
Low molecular weight chitosan--preparation with the aid of pepsin, characterization, and its bactericidal activity.

Biomacromolecules. 2007-2

[5]
Sulfated chitin and chitosan as novel biomaterials.

Int J Biol Macromol. 2007-2-20

[6]
Kinetic studies on the interactions of heparin and complement proteins using surface plasmon resonance.

Biochim Biophys Acta. 2005-11-15

[7]
Non-specific depolymerization of chitosan by pronase and characterization of the resultant products.

Eur J Biochem. 2004-2

[8]
Low molecular weight chitosans: preparation with the aid of papain and characterization.

Biochim Biophys Acta. 2004-1-22

[9]
Influence of functional groups on the in vitro anticoagulant activity of chitosan sulfate.

Carbohydr Res. 2003-3-14

[10]
Preparation of water-soluble chitosan/heparin complex and its application as wound healing accelerator.

Biomaterials. 2003-4

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