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Chapter 3. Voltage‐Dependent Ion Channels Induced by Cyclic Lipodepsipeptides in Planar Lipid Bilayers: Structure, Properties, and Resemblance to Native Channels. / Malev, Valery V.; Ostroumova, Olga S.; Takemoto, Jon Y.; Schagina, Ludmila V.

Advances in Planar Lipid Bilayers and Liposomes. Vol 8. Elsevier, 2008. стр. 292, 59-106.

Результаты исследований: Публикации в книгах, отчётах, сборниках, трудах конференцийглава/разделнаучная

Harvard

Malev, VV, Ostroumova, OS, Takemoto, JY & Schagina, LV 2008, Chapter 3. Voltage‐Dependent Ion Channels Induced by Cyclic Lipodepsipeptides in Planar Lipid Bilayers: Structure, Properties, and Resemblance to Native Channels. в Advances in Planar Lipid Bilayers and Liposomes. Vol 8. Elsevier, стр. 292, 59-106.

APA

Malev, V. V., Ostroumova, O. S., Takemoto, J. Y., & Schagina, L. V. (2008). Chapter 3. Voltage‐Dependent Ion Channels Induced by Cyclic Lipodepsipeptides in Planar Lipid Bilayers: Structure, Properties, and Resemblance to Native Channels. в Advances in Planar Lipid Bilayers and Liposomes. Vol 8 (стр. 292, 59-106). Elsevier.

Vancouver

Malev VV, Ostroumova OS, Takemoto JY, Schagina LV. Chapter 3. Voltage‐Dependent Ion Channels Induced by Cyclic Lipodepsipeptides in Planar Lipid Bilayers: Structure, Properties, and Resemblance to Native Channels. в Advances in Planar Lipid Bilayers and Liposomes. Vol 8. Elsevier. 2008. стр. 292, 59-106

Author

Malev, Valery V. ; Ostroumova, Olga S. ; Takemoto, Jon Y. ; Schagina, Ludmila V. / Chapter 3. Voltage‐Dependent Ion Channels Induced by Cyclic Lipodepsipeptides in Planar Lipid Bilayers: Structure, Properties, and Resemblance to Native Channels. Advances in Planar Lipid Bilayers and Liposomes. Vol 8. Elsevier, 2008. стр. 292, 59-106

BibTeX

@inbook{5b8aff10a92d46ddab8bc230a245a56d,
title = "Chapter 3. Voltage‐Dependent Ion Channels Induced by Cyclic Lipodepsipeptides in Planar Lipid Bilayers: Structure, Properties, and Resemblance to Native Channels",
abstract = "The syringomycins (SRs) are cyclic lipodepsipeptides produced by the phytopathogenic bacterium Pseudomonas syringae pv. syringae. Discovered and described during the 1980s and 1990s, the effects of the SRs on plant cells and inhibition of fungal and yeast growth are due to specific interactions with membrane lipids of target cells. Using one‐side addition of SRs to a system consisting of a bilayer lipid membrane and two aqueous compartments, researchers have shown that the SRs form anion selective channels that possess unique and highly reproducible voltage sensitive properties. Moreover, SRs form two types of ion channels, namely “small” and “large,” that differ several‐fold in their conductance. These initial findings generated interest in the SRs to (1) consider development of the SRs as antifungal agents, and (2) use SR channels as mechanistic models for native ion channels. Follow‐up kinetic studies were conducted on the opening/closure of ion channels formed by the most abundant form of the SRs, syringo",
author = "Malev, {Valery V.} and Ostroumova, {Olga S.} and Takemoto, {Jon Y.} and Schagina, {Ludmila V.}",
year = "2008",
language = "English",
isbn = "978-0-12-374341-1",
pages = "292, 59--106",
booktitle = "Advances in Planar Lipid Bilayers and Liposomes. Vol 8",
publisher = "Elsevier",
address = "Netherlands",

}

RIS

TY - CHAP

T1 - Chapter 3. Voltage‐Dependent Ion Channels Induced by Cyclic Lipodepsipeptides in Planar Lipid Bilayers: Structure, Properties, and Resemblance to Native Channels

AU - Malev, Valery V.

AU - Ostroumova, Olga S.

AU - Takemoto, Jon Y.

AU - Schagina, Ludmila V.

PY - 2008

Y1 - 2008

N2 - The syringomycins (SRs) are cyclic lipodepsipeptides produced by the phytopathogenic bacterium Pseudomonas syringae pv. syringae. Discovered and described during the 1980s and 1990s, the effects of the SRs on plant cells and inhibition of fungal and yeast growth are due to specific interactions with membrane lipids of target cells. Using one‐side addition of SRs to a system consisting of a bilayer lipid membrane and two aqueous compartments, researchers have shown that the SRs form anion selective channels that possess unique and highly reproducible voltage sensitive properties. Moreover, SRs form two types of ion channels, namely “small” and “large,” that differ several‐fold in their conductance. These initial findings generated interest in the SRs to (1) consider development of the SRs as antifungal agents, and (2) use SR channels as mechanistic models for native ion channels. Follow‐up kinetic studies were conducted on the opening/closure of ion channels formed by the most abundant form of the SRs, syringo

AB - The syringomycins (SRs) are cyclic lipodepsipeptides produced by the phytopathogenic bacterium Pseudomonas syringae pv. syringae. Discovered and described during the 1980s and 1990s, the effects of the SRs on plant cells and inhibition of fungal and yeast growth are due to specific interactions with membrane lipids of target cells. Using one‐side addition of SRs to a system consisting of a bilayer lipid membrane and two aqueous compartments, researchers have shown that the SRs form anion selective channels that possess unique and highly reproducible voltage sensitive properties. Moreover, SRs form two types of ion channels, namely “small” and “large,” that differ several‐fold in their conductance. These initial findings generated interest in the SRs to (1) consider development of the SRs as antifungal agents, and (2) use SR channels as mechanistic models for native ion channels. Follow‐up kinetic studies were conducted on the opening/closure of ion channels formed by the most abundant form of the SRs, syringo

M3 - Chapter

SN - 978-0-12-374341-1

SP - 292, 59-106

BT - Advances in Planar Lipid Bilayers and Liposomes. Vol 8

PB - Elsevier

ER -

ID: 4418454