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本文引用的文献

1
Single-molecule mass spectrometry in solution using a solitary nanopore.使用单个纳米孔进行溶液中的单分子质谱分析。
Proc Natl Acad Sci U S A. 2007 May 15;104(20):8207-11. doi: 10.1073/pnas.0611085104. Epub 2007 May 9.
2
Anthrax edema factor, voltage-dependent binding to the protective antigen ion channel and comparison to LF binding.炭疽水肿因子,与保护性抗原离子通道的电压依赖性结合及与致死因子结合的比较。
J Biol Chem. 2006 Oct 27;281(43):32335-43. doi: 10.1074/jbc.M606552200. Epub 2006 Sep 5.
3
Single polymer molecules in a protein nanopore in the limit of a strong polymer-pore attraction.在聚合物与纳米孔之间存在强吸引力的情况下,蛋白质纳米孔中的单个聚合物分子。
Phys Rev Lett. 2006 Jul 7;97(1):018301. doi: 10.1103/PhysRevLett.97.018301. Epub 2006 Jul 5.
4
Nonideality of polymer solutions in the pore and concentration-dependent partitioning.孔隙中聚合物溶液的非理想性及浓度依赖性分配。
J Chem Phys. 2005 Oct 8;123(14):146101. doi: 10.1063/1.2052589.
5
Anthrax biosensor, protective antigen ion channel asymmetric blockade.炭疽生物传感器,保护性抗原离子通道不对称阻断
J Biol Chem. 2005 Oct 7;280(40):34056-62. doi: 10.1074/jbc.M507928200. Epub 2005 Aug 8.
6
A phenylalanine clamp catalyzes protein translocation through the anthrax toxin pore.苯丙氨酸钳催化蛋白质通过炭疽毒素孔道进行转运。
Science. 2005 Jul 29;309(5735):777-81. doi: 10.1126/science.1113380.
7
Purified Bacillus anthracis lethal toxin complex formed in vitro and during infection exhibits functional and biological activity.在体外形成以及在感染过程中形成的纯化炭疽芽孢杆菌致死毒素复合物具有功能和生物活性。
J Biol Chem. 2005 Mar 18;280(11):10834-9. doi: 10.1074/jbc.M412210200. Epub 2005 Jan 11.
8
Anthrax toxin protective antigen: inhibition of channel function by chloroquine and related compounds and study of binding kinetics using the current noise analysis.炭疽毒素保护性抗原:氯喹及相关化合物对通道功能的抑制作用以及利用电流噪声分析对结合动力学的研究
Biophys J. 2005 Mar;88(3):1715-24. doi: 10.1529/biophysj.104.050336. Epub 2004 Dec 13.
9
Sizing the pore of the volume-sensitive anion channel by differential polymer partitioning.通过差异聚合物分配法确定容积敏感性阴离子通道的孔径
FEBS Lett. 2004 Oct 22;576(3):433-6. doi: 10.1016/j.febslet.2004.09.051.
10
Three-dimensional model of the pore form of anthrax protective antigen. Structure and biological implications.炭疽保护性抗原孔道形式的三维模型。结构与生物学意义。
J Biomol Struct Dyn. 2004 Dec;22(3):253-65. doi: 10.1080/07391102.2004.10531226.

用非电解质聚乙二醇确定炭疽芽孢杆菌PA63通道的大小。

Sizing the Bacillus anthracis PA63 channel with nonelectrolyte poly(ethylene glycols).

作者信息

Nablo Brian J, Halverson Kelly M, Robertson Joseph W F, Nguyen Tam L, Panchal Rekha G, Gussio Rick, Bavari Sina, Krasilnikov Oleg V, Kasianowicz John J

机构信息

Electrical and Electronics Laboratory, Semiconductor Electronics Division, National Institute of Standards and Technology, Gaithersburg, Maryland 20899-8120, USA.

出版信息

Biophys J. 2008 Aug;95(3):1157-64. doi: 10.1529/biophysj.107.121715.

DOI:10.1529/biophysj.107.121715
PMID:18645196
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2479592/
Abstract

Nonelectrolyte polymers of poly(ethylene glycol) (PEG) were used to estimate the diameter of the ion channel formed by the Bacillus anthracis protective antigen 63 (PA(63)). Based on the ability of different molecular weight PEGs to partition into the pore and reduce channel conductance, the pore appears to be narrower than the one formed by Staphylococcus aureus alpha-hemolysin. Numerical integration of the PEG sample mass spectra and the channel conductance data were used to refine the estimate of the pore's PEG molecular mass cutoff (approximately 1400 g/mol). The results suggest that the limiting diameter of the PA(63) pore is <2 nm, which is consistent with an all-atom model of the PA(63) channel and previous experiments using large ions.

摘要

聚乙二醇(PEG)的非电解质聚合物被用于估算炭疽芽孢杆菌保护性抗原63(PA(63))形成的离子通道直径。基于不同分子量PEG进入孔道并降低通道电导率的能力,该孔道似乎比金黄色葡萄球菌α-溶血素形成的孔道更窄。对PEG样品质谱和通道电导率数据进行数值积分,以优化对孔道PEG分子量截止值(约1400 g/mol)的估计。结果表明,PA(63)孔道的极限直径小于2 nm,这与PA(63)通道的全原子模型以及先前使用大离子的实验结果一致。