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肝素寡糖增强组织型纤溶酶原激活剂:寡糖长度与纤溶酶原激活刺激之间的相关性。

Heparin oligosaccharides enhance tissue-type plasminogen activator: a correlation between oligosaccharide length and stimulation of plasminogen activation.

作者信息

Edelberg J M, Conrad H E, Pizzo S V

机构信息

Department of Pathology, Duke University Medical Center, Durham, North Carolina 27710.

出版信息

Biochemistry. 1991 Nov 12;30(45):10999-1003. doi: 10.1021/bi00109a027.

Abstract

The rate of plasminogen (Pg) activation by tissue-type Pg activator (t-PA) is enhanced by heparin-derived oligosaccharides. Kinetic analysis of the effects of heparin oligosaccharides, ranging in size from di- to dodecasaccharides, on Pg activation demonstrates that stimulation of the reaction is dependent on the size of the heparin oligosaccharides. Di- and tetrasaccharides enhance the activation through 2-fold increases in kcat and 4-fold decreases in Km. Hexasaccharide and larger oligosaccharides stimulate the reaction by increasing the kcat by as much as 4-fold, but do not affect the Km. Previous experiments have shown that lipoprotein(a) [Lp(a)] inhibits Pg activation by t-PA, but only in the presence of a template which enhances t-PA activity such as fibrinogen fragments or intact heparin. Similiarly, Lp(a) inhibits the enhancement of t-PA activity by the larger heparin oligosaccharides but has no effect on t-PA activity in the presence of di- and tetrasaccharides. The results of this study when considered with our previous observations (Edelberg & Pizzo, 1990) suggest that the enhancement in Pg activation by the smaller oligosaccharides is mediated exclusively via binding to t-PA while the larger oligosaccharides may interact with both t-PA and Pg. Furthermore, studies of Pg activation in the presence of both heparin oligosaccharides and fibrinogen fragments demonstrate that t-PA is stimulated preferentially by fibrinogen fragments.

摘要

肝素衍生的寡糖可增强组织型纤溶酶原激活剂(t-PA)对纤溶酶原(Pg)的激活速率。对大小从二糖到十二糖不等的肝素寡糖对Pg激活作用的动力学分析表明,反应的刺激作用取决于肝素寡糖的大小。二糖和四糖通过使催化常数(kcat)增加2倍和米氏常数(Km)降低4倍来增强激活作用。六糖及更大的寡糖通过使kcat增加多达4倍来刺激反应,但不影响Km。先前的实验表明,脂蛋白(a)[Lp(a)]抑制t-PA对Pg的激活,但仅在存在增强t-PA活性的模板(如纤维蛋白原片段或完整肝素)时才会发生。同样,Lp(a)抑制较大肝素寡糖对t-PA活性的增强作用,但在存在二糖和四糖时对t-PA活性没有影响。将本研究结果与我们先前的观察结果(埃德尔伯格和皮佐,1990年)相结合表明,较小寡糖对Pg激活的增强作用仅通过与t-PA结合介导,而较大寡糖可能与t-PA和Pg都相互作用。此外,在同时存在肝素寡糖和纤维蛋白原片段的情况下对Pg激活的研究表明,纤维蛋白原片段优先刺激t-PA。

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