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本文引用的文献

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A biologically active surface enzyme assembly that attenuates thrombus formation.一种可减弱血栓形成的生物活性表面酶组装体。
Adv Funct Mater. 2011 Dec 20;21(24):4736-4743. doi: 10.1002/adfm.201101687. Epub 2011 Sep 26.
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Polymeric conjugates for drug delivery.用于药物递送的聚合物缀合物。
Chem Mater. 2012 Mar 13;24(5):840-853. doi: 10.1021/cm2031569. Epub 2012 Jan 4.
3
Protein thioester synthesis enabled by sortase.通过 sortase 实现的蛋白质硫酯合成。
J Am Chem Soc. 2012 Jul 4;134(26):10749-52. doi: 10.1021/ja302354v. Epub 2012 Jun 19.
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Nonhuman primate models of thrombosis.非人类灵长类动物血栓模型。
Thromb Res. 2012 May;129 Suppl 2:S65-9. doi: 10.1016/j.thromres.2012.02.037. Epub 2012 Mar 10.
5
Results of heparin-bonded ePTFE-covered stents for chronic occlusive superficial femoral artery disease.肝素结合 ePTFE 覆膜支架治疗慢性闭塞性股浅动脉疾病的结果。
J Vasc Surg. 2012 Jul;56(1):118-25. doi: 10.1016/j.jvs.2011.12.066. Epub 2012 Feb 17.
6
The use of antithrombotic therapies in reducing synthetic small-diameter vascular graft thrombosis.抗血栓治疗在减少人工合成小口径血管移植物血栓形成中的应用。
Vasc Endovascular Surg. 2012 Apr;46(3):212-22. doi: 10.1177/1538574411433299. Epub 2012 Feb 5.
7
Radiation and ethylene oxide terminal sterilization experiences with drug eluting stent products.药物洗脱支架产品的辐照和环氧乙烷终端灭菌经验。
AAPS PharmSciTech. 2011 Dec;12(4):1116-26. doi: 10.1208/s12249-011-9644-8. Epub 2011 Sep 2.
8
Thrombomodulin and its role in inflammation.血栓调节蛋白及其在炎症中的作用。
Semin Immunopathol. 2012 Jan;34(1):107-25. doi: 10.1007/s00281-011-0282-8. Epub 2011 Jul 31.
9
A general strategy for the evolution of bond-forming enzymes using yeast display.利用酵母展示进化成键合酶的一般策略。
Proc Natl Acad Sci U S A. 2011 Jul 12;108(28):11399-404. doi: 10.1073/pnas.1101046108. Epub 2011 Jun 22.
10
Nonthrombogenic approaches to cardiovascular bioengineering.心血管生物工程中的非血栓形成方法。
Annu Rev Biomed Eng. 2011 Aug 15;13:451-75. doi: 10.1146/annurev-bioeng-071910-124733.

在无菌的血液接触面固定具有主动抗血栓功能的组件。

Immobilization of actively thromboresistant assemblies on sterile blood-contacting surfaces.

机构信息

Department of Surgery, Beth Israel Deaconess Medical Center, Harvard Medical School and the Wyss Institute of Biologically Inspired, Engineering of Harvard University, Boston, MA 02115, USA; Coulter Department of Biomedical Engineering, Petit Institute for Bioengineering and Bioscience, Georgia Institute of Technology, Atlanta, GA 30332, USA.

出版信息

Adv Healthc Mater. 2014 Jan;3(1):30-5. doi: 10.1002/adhm.201300110. Epub 2013 Jun 21.

DOI:10.1002/adhm.201300110
PMID:23788402
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3955951/
Abstract

Rapid one-step modification of thrombomodulin with alkylamine derivatives such as azide, biotin, and PEG is achieved using an evolved sortase (eSrtA) mutant. The feasibility of a point-of-care scheme is demonstrated herein to site-specifically immobilize azido-thrombomodulin on sterilized commercial ePTFE vascular grafts, which exhibit superior thromboresistance compared with commercial heparin-coated grafts in a primate model of acute graft thrombosis.

摘要

使用经过改造的 sortase(eSrtA)突变体,可以快速一步将血栓调节蛋白与烷基胺衍生物(如叠氮化物、生物素和 PEG)进行修饰。本文证明了一种即时护理方案的可行性,即通过定点将叠氮化物-血栓调节蛋白固定在经过消毒的商用 ePTFE 血管移植物上,与商用肝素涂覆的移植物相比,在灵长类动物急性移植物血栓形成模型中,该移植物具有更好的抗血栓性。