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1
Apparent inhibition of photoredox reactions of magnesium octaethylporphyrin at the lipid bilayer-water interface by neutral quinones.中性醌类物质对八乙基镁卟啉在脂质双层-水界面光氧化还原反应的明显抑制作用。
Biophys J. 1981 Jul;35(1):93-7. doi: 10.1016/S0006-3495(81)84776-5.
2
The potential span of photoredox reactions of porphyrins and chlorophyll at the lipid bilayer-water interface.卟啉和叶绿素在脂质双分子层 - 水界面处光氧化还原反应的潜在跨度。
Biophys J. 1981 Jul;35(1):79-92. doi: 10.1016/S0006-3495(81)84775-3.
3
Photoinduced electron transfer across lipid bilayers containing magnesium octaethylporphyrin.光诱导电子穿过含八乙基镁卟啉的脂质双层的转移。
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4
Photoinitiated ion movements in bilayer membranes containing magnesium octaethylporphyrin.含八乙基镁卟啉的双层膜中的光引发离子运动。
Biophys J. 1986 Sep;50(3):431-9. doi: 10.1016/S0006-3495(86)83479-8.
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Charge transfer across a single lipid-water interface causes ion pumping across the bilayer.电荷在单个脂质-水界面间的转移导致离子跨双层膜的泵浦。
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Diffusion- and reaction rate-limited redox processes mediated by quinones through bilayer lipid membranes.醌类物质通过双层脂质膜介导的扩散和反应速率受限的氧化还原过程。
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The effect of oxygen on the amplitude of photodriven electron transfer across the lipid bilayer-water interface.氧气对跨脂质双层 - 水界面的光驱动电子转移幅度的影响。
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Kinetics of charge transfer at the lipid bilayer-water interface on the nanosecond time scale.纳秒时间尺度下脂质双分子层-水界面处的电荷转移动力学。
Biophys J. 1987 Oct;52(4):577-86. doi: 10.1016/S0006-3495(87)83247-2.
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Photoinitiated vectorial transmembrane electron transfer in bilayers sensitized by a face to face triporphyrin acting as a molecular electronic device. Amplification due to ionic coupling.由面对面的三卟啉作为分子电子器件敏化的双层膜中的光引发矢量跨膜电子转移。离子耦合导致的放大作用。
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Protein/lipid interaction in the bacterial photosynthetic reaction center: phosphatidylcholine and phosphatidylglycerol modify the free energy levels of the quinones.细菌光合反应中心中的蛋白质/脂质相互作用:磷脂酰胆碱和磷脂酰甘油改变醌的自由能水平。
Biochemistry. 2004 Oct 12;43(40):12913-23. doi: 10.1021/bi0489356.

引用本文的文献

1
The potential span of photoredox reactions of porphyrins and chlorophyll at the lipid bilayer-water interface.卟啉和叶绿素在脂质双分子层 - 水界面处光氧化还原反应的潜在跨度。
Biophys J. 1981 Jul;35(1):79-92. doi: 10.1016/S0006-3495(81)84775-3.
2
The effect of oxygen on the amplitude of photodriven electron transfer across the lipid bilayer-water interface.氧气对跨脂质双层 - 水界面的光驱动电子转移幅度的影响。
Biophys J. 1985 May;47(5):679-84. doi: 10.1016/S0006-3495(85)83964-3.
3
Diffusion- and reaction rate-limited redox processes mediated by quinones through bilayer lipid membranes.醌类物质通过双层脂质膜介导的扩散和反应速率受限的氧化还原过程。
Biophys J. 1987 Feb;51(2):161-7. doi: 10.1016/S0006-3495(87)83321-0.

本文引用的文献

1
The potential span of photoredox reactions of porphyrins and chlorophyll at the lipid bilayer-water interface.卟啉和叶绿素在脂质双分子层 - 水界面处光氧化还原反应的潜在跨度。
Biophys J. 1981 Jul;35(1):79-92. doi: 10.1016/S0006-3495(81)84775-3.
2
Potential energy barriers to ion transport within lipid bilayers. Studies with tetraphenylborate.脂质双分子层中离子运输的势能屏障。四苯硼酸盐的研究。
Biophys J. 1975 Aug;15(8):795-830. doi: 10.1016/S0006-3495(75)85856-5.
3
Plasto- and ubiquinone as translocators of electrons and protons through membranes: a facilitating role of the isoprenoid side chain.质体醌和泛醌作为电子和质子通过膜的转运体:类异戊二烯侧链的促进作用。
FEBS Lett. 1977 Jul 15;79(2):345-7. doi: 10.1016/0014-5793(77)80817-x.

中性醌类物质对八乙基镁卟啉在脂质双层-水界面光氧化还原反应的明显抑制作用。

Apparent inhibition of photoredox reactions of magnesium octaethylporphyrin at the lipid bilayer-water interface by neutral quinones.

作者信息

Krakover T, Ilani A, Mauzerall D

出版信息

Biophys J. 1981 Jul;35(1):93-7. doi: 10.1016/S0006-3495(81)84776-5.

DOI:10.1016/S0006-3495(81)84776-5
PMID:7260323
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1327505/
Abstract

Neutral quinones rapidly equilibrate across the lipid bilayer, hereby rendering the photoeffects seen in pigmented bilayers sensitive to the redox properties at both interfaces. The lack of photoeffect by quinones themselves and their apparent quenching reactions with aqueous acceptors is thus explained. An aqueous donor is needed on one side to break the symmetry and to allow vectorial electron transfer to be recorded. It is concluded that the neutral quinone accumulates on the polar side of the interface with respect to the hydrophobic pigment. The system may allow the study of kinetics of proton transfer accompanying the redox reactions of the quinones.

摘要

中性醌能迅速在脂质双分子层间达到平衡,从而使色素双分子层中观察到的光效应取决于两个界面处的氧化还原特性。由此解释了醌本身缺乏光效应以及它们与水性受体明显的猝灭反应。一侧需要有一个水性供体来打破对称性,并记录矢量电子转移。得出的结论是,相对于疏水性色素,中性醌在界面的极性侧积累。该系统可能有助于研究醌氧化还原反应伴随的质子转移动力学。