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Development of Antifouling Hyperbranched Polyglycerol Layers on Hydroxyl Poly-p-xylylene Coatings.在羟基聚对二甲苯涂层上开发防污超支化聚甘油层。
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2
Application of advanced sampling and analysis methods to predict the structure of adsorbed protein on a material surface.应用先进的采样和分析方法预测材料表面吸附蛋白质的结构。
Biointerphases. 2017 May 17;12(2):02D409. doi: 10.1116/1.4983274.
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A Facile and Versatile Method to Endow Biomaterial Devices with Zwitterionic Surface Coatings.一种赋予生物材料装置两性离子表面涂层的简便通用方法。
Adv Healthc Mater. 2017 Feb;6(4). doi: 10.1002/adhm.201601091. Epub 2016 Dec 15.
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The early days of PEG and PEGylation (1970s-1990s).
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Modeling and simulation of protein-surface interactions: achievements and challenges.蛋白质-表面相互作用的建模与模拟:成就与挑战
Q Rev Biophys. 2016;49:e4. doi: 10.1017/S0033583515000256.
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The Langmuir isotherm: a commonly applied but misleading approach for the analysis of protein adsorption behavior.朗缪尔等温线:一种常用于分析蛋白质吸附行为但具有误导性的方法。
J Biomed Mater Res A. 2015 Mar;103(3):949-58. doi: 10.1002/jbm.a.35235. Epub 2014 Jun 3.
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Zwitterionic hydrogels implanted in mice resist the foreign-body reaction.两性离子水凝胶植入小鼠后可抵抗异物反应。
Nat Biotechnol. 2013 Jun;31(6):553-6. doi: 10.1038/nbt.2580. Epub 2013 May 12.
8
Non-fouling biomaterials based on blends of polyethylene oxide copolymers and polyurethane: simultaneous measurement of platelet adhesion and fibrinogen adsorption from flowing whole blood.基于聚氧化乙烯共聚物和聚氨酯共混物的抗污生物材料:从流动全血中同时测量血小板黏附和纤维蛋白原吸附。
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Protein interactions with surfaces: Computational approaches and repellency.蛋白质与表面的相互作用:计算方法与斥水性。
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Complement activation on poly(ethylene oxide)-like radiofrequency glow discharge-deposited surfaces.聚环氧乙烷样射频辉光放电沉积表面的补体激活。
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纤维蛋白原在生物材料上的吸附。

Fibrinogen adsorption to biomaterials.

机构信息

Departments of Bioengineering and Chemical Engineering, University of Washington, Seattle, Washington 98195.

出版信息

J Biomed Mater Res A. 2018 Oct;106(10):2777-2788. doi: 10.1002/jbm.a.36460. Epub 2018 Sep 8.

DOI:10.1002/jbm.a.36460
PMID:29896846
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6202247/
Abstract

Fibrinogen (Fg) adsorption is an important mechanism underlying cell adhesion to biomaterials and was the major focus of the author's research career. This article summarizes our work on Fg adsorption, with citations of related work as appropriate. The molecular properties of Fg that promote adsorption and cell adhesion will be described. In addition, the adsorption behavior of Fg from buffer, binary solutions with other proteins, and blood plasma will be discussed, including the Vroman effect. Studies of platelet adhesion to surfaces preadsorbed with blood plasmas selectively deficient in Fg, vitronectin (Vn), fibronectin (Fn), or von Willebrand's factor (vWf) will be reviewed. These studies clearly showed a major role for Fg in platelet adhesion under static conditions and both Fg and vWf for adhesion from flowing suspensions, but no significant role for Vn or Fn. However, it was also shown that platelet adhesion was poorly correlated with the total amount of adsorbed Fg, but very well correlated with the binding of antibodies specific to the cell binding domains of Fg. A brief overview of nonfouling surfaces for prevention of Fg adsorption will be given. A more extensive discussion of structural changes in Fg after its adsorption is included, including changes detected with both physicochemical and biological methods. A short discussion of the state of the art of structural determination of adsorbed proteins with computational methods is also given. A final section identifies Fg adsorption as the single most important event determining the biocompatibility of implants in soft tissue and in blood. © 2018 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 106A: 2777-2788, 2018.

摘要

纤维蛋白原(Fg)吸附是细胞黏附于生物材料的重要机制,也是作者研究工作的主要重点。本文总结了作者在纤维蛋白原吸附方面的工作,并适当引用了相关工作。将描述促进吸附和细胞黏附的纤维蛋白原的分子特性。此外,还将讨论从缓冲液、与其他蛋白质的二元溶液和血浆中吸附纤维蛋白原的行为,包括 Vroman 效应。综述了血小板黏附于预先吸附有纤维蛋白原、玻连蛋白(Vn)、纤维连接蛋白(Fn)或血管性血友病因子(vWf)缺陷的血浆的表面的研究。这些研究清楚地表明,纤维蛋白原在静态条件下对血小板黏附起主要作用,纤维蛋白原和 vWf 在流动悬浮液中对黏附起作用,但 Vn 或 Fn 没有明显作用。然而,研究还表明,血小板黏附与吸附的纤维蛋白原总量相关性较差,但与针对纤维蛋白原细胞结合结构域的抗体结合相关性非常好。本文简要概述了用于防止纤维蛋白原吸附的非缠结表面。还包括了纤维蛋白原吸附后结构变化的更广泛讨论,包括使用物理化学和生物学方法检测到的变化。还简要讨论了使用计算方法确定吸附蛋白质结构的最新技术。最后一部分将纤维蛋白原吸附确定为决定软组织和血液中植入物生物相容性的唯一最重要事件。© 2018 威利父子公司