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本文引用的文献

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A demonstration of some new methods of determining molecular weights from the data of the ultracentrifuge.
J Phys Colloid Chem. 1947 Sep;51(5):1204-13. doi: 10.1021/j150455a014.
2
Monitoring the homogeneity of adenovirus preparations (a gene therapy delivery system) using analytical ultracentrifugation.使用分析型超速离心法监测腺病毒制剂(一种基因治疗递送系统)的均匀性。
Anal Biochem. 2007 Mar 1;362(1):16-37. doi: 10.1016/j.ab.2006.11.031. Epub 2006 Dec 20.
3
Crystal structure of the Tp34 (TP0971) lipoprotein of treponema pallidum: implications of its metal-bound state and affinity for human lactoferrin.梅毒螺旋体Tp34(TP0971)脂蛋白的晶体结构:其金属结合状态及对人乳铁蛋白亲和力的意义
J Biol Chem. 2007 Feb 23;282(8):5944-58. doi: 10.1074/jbc.M610215200. Epub 2006 Dec 27.
4
Quantitation of aggregate levels in a recombinant humanized monoclonal antibody formulation by size-exclusion chromatography, asymmetrical flow field flow fractionation, and sedimentation velocity.通过尺寸排阻色谱法、不对称流场流分级法和沉降速度法对重组人源化单克隆抗体制剂中的聚集体水平进行定量分析。
J Pharm Sci. 2007 Feb;96(2):268-79. doi: 10.1002/jps.20760.
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Sedimentation velocity analysis of amyloid oligomers and fibrils.淀粉样寡聚体和原纤维的沉降速度分析
Methods Enzymol. 2006;413:199-217. doi: 10.1016/S0076-6879(06)13011-6.
6
Role of analytical ultracentrifugation in assessing the aggregation of protein biopharmaceuticals.分析超速离心法在评估蛋白质生物制药聚集方面的作用。
AAPS J. 2006 Sep 22;8(3):E590-605. doi: 10.1208/aapsj080368.
7
A critical review of analytical ultracentrifugation and field flow fractionation methods for measuring protein aggregation.用于测量蛋白质聚集的分析超速离心法和场流分级法的批判性综述。
AAPS J. 2006 Sep 22;8(3):E580-9. doi: 10.1208/aapsj080367.
8
Effects of protein aggregates: an immunologic perspective.蛋白质聚集体的影响:免疫学视角
AAPS J. 2006 Aug 4;8(3):E501-7. doi: 10.1208/aapsj080359.
9
An approximate solution to the Lamm equation.拉姆方程的近似解。
Biophys Chem. 1979 Sep;10(2):187-90. doi: 10.1016/0301-4622(79)85039-5.
10
Analytical ultracentrifugation for the study of protein association and assembly.用于研究蛋白质缔合与组装的分析超速离心法。
Curr Opin Chem Biol. 2006 Oct;10(5):430-6. doi: 10.1016/j.cbpa.2006.08.017. Epub 2006 Aug 28.

一种用于分析超速离心沉降速度分布模拟的新型自适应网格尺寸算法。

A new adaptive grid-size algorithm for the simulation of sedimentation velocity profiles in analytical ultracentrifugation.

作者信息

Brown Patrick H, Schuck Peter

机构信息

National Institute of Biomedical Imaging and Bioengineering, National Institutes of Health, Bethesda, Maryland, MD 20892.

出版信息

Comput Phys Commun. 2008 Jan 15;178(2):105-120. doi: 10.1016/j.cpc.2007.08.012.

DOI:10.1016/j.cpc.2007.08.012
PMID:18196178
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2267755/
Abstract

Analytical ultracentrifugation allows one to measure in real-time the concentration gradients arising from the application of a centrifugal force to macromolecular mixtures in solution. In the last decade, the ability to efficiently solve the partial differential equation governing the ultracentrifugal sedimentation and diffusion process, the Lamm equation, has spawned significant progress in the application of sedimentation velocity analytical ultracentrifugation for the study of biological macromolecules, for example, the characterization of protein oligomeric states and the study of reversible multi-protein complexes in solution. The present work describes a numerical algorithm that can provide an improvement in accuracy or efficiency over existing algorithms by more than one order of magnitude, and thereby greatly facilitate the practical application of sedimentation velocity analysis, in particular, for the study of multi-component macromolecular mixtures. It is implemented in the public domain software SEDFIT for the analysis of experimental data.

摘要

分析超速离心法可让人们实时测量因对溶液中的大分子混合物施加离心力而产生的浓度梯度。在过去十年中,能够有效求解描述超速离心沉降和扩散过程的偏微分方程(即兰姆方程),在沉降速度分析超速离心法用于研究生物大分子方面取得了重大进展,例如,蛋白质寡聚状态的表征以及溶液中可逆多蛋白复合物的研究。本研究描述了一种数值算法,该算法在准确性或效率方面比现有算法提高了一个多数量级,从而极大地促进了沉降速度分析的实际应用,特别是对于多组分大分子混合物的研究。它在用于分析实验数据的公共领域软件SEDFIT中得以实现。