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本文引用的文献

1
In vivo protein architecture of the eukaryotic kinetochore with nanometer scale accuracy.真核生物动粒的体内蛋白质结构,精度达纳米级别。
Curr Biol. 2009 Apr 28;19(8):694-9. doi: 10.1016/j.cub.2009.02.056. Epub 2009 Apr 2.
2
High precision size measurement of centromere 8 and the 8q24/c-myc gene region in metaphase and interphase human fibroblasts indicate differential condensation.中期和间期人成纤维细胞着丝粒 8 和 8q24/c-myc 基因区域的高精度大小测量表明存在差异凝聚。
J Struct Biol. 2008 Dec;164(3):293-303. doi: 10.1016/j.jsb.2008.09.002. Epub 2008 Sep 19.
3
Dynamic imaging of fibrin network formation correlated with other measures of polymerization.纤维蛋白网络形成的动态成像与其他聚合指标相关。
Blood. 2008 May 15;111(10):4854-61. doi: 10.1182/blood-2007-08-105247. Epub 2008 Feb 13.
4
Evaluating performance in three-dimensional fluorescence microscopy.评估三维荧光显微镜下的性能。
J Microsc. 2007 Dec;228(Pt 3):390-405. doi: 10.1111/j.1365-2818.2007.01861.x.
5
Nanostructure analysis using spatially modulated illumination microscopy.使用空间调制照明显微镜进行纳米结构分析。
Nat Protoc. 2007;2(10):2640-6. doi: 10.1038/nprot.2007.399.
6
4Pi microscopy deconvolution with a variable point-spread function.具有可变点扩散函数的4Pi显微镜解卷积
Appl Opt. 2006 Sep 20;45(27):7056-64. doi: 10.1364/ao.45.007056.
7
Polymerization of fibrin: specificity, strength, and stability of knob-hole interactions studied at the single-molecule level.纤维蛋白的聚合:在单分子水平上研究的钮孔相互作用的特异性、强度和稳定性。
Blood. 2005 Nov 1;106(9):2944-51. doi: 10.1182/blood-2005-05-2039. Epub 2005 Jul 5.
8
Dynamic changes of fibrin architecture during fibrin formation and intrinsic fibrinolysis of fibrin-rich clots.富含纤维蛋白凝块在纤维蛋白形成和内源性纤维蛋白溶解过程中纤维蛋白结构的动态变化。
J Biol Chem. 2003 Jun 13;278(24):21331-5. doi: 10.1074/jbc.M212734200. Epub 2003 Mar 17.
9
Formation of fibrin gel in fibrinogen-thrombin system: static and dynamic light scattering study.纤维蛋白原-凝血酶系统中纤维蛋白凝胶的形成:静态和动态光散射研究
Biomacromolecules. 2002 Sep-Oct;3(5):1013-20. doi: 10.1021/bm025545v.
10
Early events in the polymerization of fibrin.纤维蛋白聚合的早期事件。
Ann N Y Acad Sci. 2001;936:167-84. doi: 10.1111/j.1749-6632.2001.tb03504.x.

可视化和鉴定纤维蛋白聚合早期形成的结构。

Visualization and identification of the structures formed during early stages of fibrin polymerization.

机构信息

Department of Cell and Developmental Biology, University of Pennsylvania School of Medicine, Philadelphia, PA, USA.

出版信息

Blood. 2011 Apr 28;117(17):4609-14. doi: 10.1182/blood-2010-07-297671. Epub 2011 Jan 19.

DOI:10.1182/blood-2010-07-297671
PMID:21248064
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3099577/
Abstract

We determined the sequence of events and identified and quantitatively characterized the mobility of moving structures present during the early stages of fibrin-clot formation from the beginning of polymerization to the gel point. Three complementary techniques were used in parallel: spinning-disk confocal microscopy, transmission electron microscopy, and turbidity measurements. At the beginning of polymerization the major structures were monomers, whereas at the middle of the lag period there were monomers, oligomers, protofibrils (defined as structures that consisted of more than 8 monomers), and fibers. At the end of the lag period, there were primarily monomers and fibers, giving way to mainly fibers at the gel point. Diffusion rates were calculated from 2 different results, one based on sizes and another on the velocity of the observed structures, with similar results in the range of 3.8-0.1 μm²/s. At the gel point, the diffusion coefficients corresponded to very large, slow-moving structures and individual protofibrils. The smallest moving structures visible by confocal microscopy during fibrin polymerization were identified as protofibrils with a length of approximately 0.5 μm. The sequence of early events of clotting and the structures present are important for understanding hemostasis and thrombosis.

摘要

我们确定了事件的顺序,并鉴定和定量描述了纤维蛋白凝块形成早期从聚合开始到凝胶点期间存在的运动结构的迁移性。三种互补技术同时使用:旋转盘共聚焦显微镜、透射电子显微镜和浊度测量。在聚合开始时,主要结构是单体,而在滞后期的中间阶段,有单体、低聚物、原纤维(定义为由超过 8 个单体组成的结构)和纤维。在滞后期末期,主要是单体和纤维,在凝胶点时主要是纤维。扩散速率是根据 2 个不同的结果计算得出的,一个基于结构的大小,另一个基于观察到的结构的速度,在 3.8-0.1 μm²/s 的范围内得到了相似的结果。在凝胶点,扩散系数对应于非常大的、移动缓慢的结构和单个原纤维。在纤维蛋白聚合过程中通过共聚焦显微镜可见的最小运动结构被鉴定为长度约为 0.5 μm 的原纤维。凝血和存在的结构的早期事件的顺序对于理解止血和血栓形成很重要。