Single channel properties of lysenin measured in artificial lipid bilayers and their applications to biomolecule detection

被引:12
作者
Aoki, Takaaki [1 ]
Hirano, Minako [2 ]
Takeuchi, Yuko [1 ]
Kobayashi, Toshihide [3 ]
Yanagida, Toshio [1 ,2 ]
Ide, Toru [1 ,4 ]
机构
[1] Osaka Univ, Grad Sch Frontier Biosci, Network Ctr Mol & Syst Life Sci, Suita, Osaka 5650871, Japan
[2] Osaka Univ, Grad Sch Frontier Biosci, Lab Nanobiol, Suita, Osaka 5650871, Japan
[3] RIKEN, Lipid Biol Lab, Saitama, Japan
[4] RIKEN, Mol Informat Life Sci Res Grp, Saitama, Japan
来源
PROCEEDINGS OF THE JAPAN ACADEMY SERIES B-PHYSICAL AND BIOLOGICAL SCIENCES | 2010年 / 86卷 / 09期
关键词
hemolytic toxin; patch clamp; single channel current; current inhibition; EISENIA-FOETIDA; SPHINGOMYELIN; MEMBRANES; PROTEIN; TOXIN; BINDING;
D O I
10.2183/pjab.86.920
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Single channel currents of lysenin were measured using artificial lipid bilayers formed on a glass micropipette tip. The single channel conductance for KCl, NaCl, CaCl2, and Trimethylammonium-Cl were 474 +/- 87, 537 +/- 66, 210 +/- 14, and 274 +/- 10 ps, respectively, while the permeability ratio P-Na/P-Cl was 5.8. By adding poly(deoxy adenine) or poly(L-lysine) to one side of the bilayer, channel currents were influenced when membrane voltages were applied to pass the charged molecules through the channel pores. Current inhibition process was concentration-dependent with applied DNA. As the current fluctuations of a-hemolysin channels is often cited as the detector in a molecular sensor, these results suggest that by monitoring channel current changes, the lysenin channel has possibilities to detect interactions between it and certain biomolecules by its current fluctuations.
引用
收藏
页码:920 / 925
页数:6
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