Mechanistic Investigation of Interactions between Steroidal Saponin Digitonin and Cell Membrane Models
Digitonin is an amphiphilic steroidal saponin, a class of natural products that can bind to cholesterol and lyse cells. Despite the known cell membrane lysis activity, it remains unclear how it interacts with cell membranes. In the present work, the interaction mechanism between digitonin and cell m...
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Veröffentlicht in: | The journal of physical chemistry. B 2014-12, Vol.118 (50), p.14632-14639 |
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creator | Frenkel, Nataliya Makky, Ali Sudji, Ikhwan Resmala Wink, Michael Tanaka, Motomu |
description | Digitonin is an amphiphilic steroidal saponin, a class of natural products that can bind to cholesterol and lyse cells. Despite the known cell membrane lysis activity, it remains unclear how it interacts with cell membranes. In the present work, the interaction mechanism between digitonin and cell membrane models has quantitatively been investigated using a combination of physical techniques. It has been demonstrated that digitonin molecules bind specifically to cholesterol in the membrane, resulting in the formation of cholesterol–digitonin complexes on the membrane surface by removing cholesterol from the membrane core. Changes in the mass density and the film mechanics caused by the digitonin were determined by using quartz crystal microbalance with dissipation (QCM-D), and the combination of X-ray reflectivity (XRR) and dual polarization interferometry (DPI) yielded the hydration level of the cholesterol–digitonin complexes. From differential scanning calorimetry (DSC) analysis, supporting evidence was obtained that cholesterol was removed from the membrane core. |
doi_str_mv | 10.1021/jp5074939 |
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Despite the known cell membrane lysis activity, it remains unclear how it interacts with cell membranes. In the present work, the interaction mechanism between digitonin and cell membrane models has quantitatively been investigated using a combination of physical techniques. It has been demonstrated that digitonin molecules bind specifically to cholesterol in the membrane, resulting in the formation of cholesterol–digitonin complexes on the membrane surface by removing cholesterol from the membrane core. Changes in the mass density and the film mechanics caused by the digitonin were determined by using quartz crystal microbalance with dissipation (QCM-D), and the combination of X-ray reflectivity (XRR) and dual polarization interferometry (DPI) yielded the hydration level of the cholesterol–digitonin complexes. 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B</title><addtitle>J. Phys. Chem. B</addtitle><description>Digitonin is an amphiphilic steroidal saponin, a class of natural products that can bind to cholesterol and lyse cells. Despite the known cell membrane lysis activity, it remains unclear how it interacts with cell membranes. In the present work, the interaction mechanism between digitonin and cell membrane models has quantitatively been investigated using a combination of physical techniques. It has been demonstrated that digitonin molecules bind specifically to cholesterol in the membrane, resulting in the formation of cholesterol–digitonin complexes on the membrane surface by removing cholesterol from the membrane core. Changes in the mass density and the film mechanics caused by the digitonin were determined by using quartz crystal microbalance with dissipation (QCM-D), and the combination of X-ray reflectivity (XRR) and dual polarization interferometry (DPI) yielded the hydration level of the cholesterol–digitonin complexes. From differential scanning calorimetry (DSC) analysis, supporting evidence was obtained that cholesterol was removed from the membrane core.</description><subject>Calorimetry, Differential Scanning</subject><subject>Cell Membrane - chemistry</subject><subject>Cell Membrane - metabolism</subject><subject>Cholesterol</subject><subject>Cholesterol - chemistry</subject><subject>Cholesterol - metabolism</subject><subject>Density</subject><subject>Differential scanning calorimetry</subject><subject>Digitonin - chemistry</subject><subject>Digitonin - metabolism</subject><subject>Interferometry - methods</subject><subject>Membranes</subject><subject>Microbalances</subject><subject>Models, Chemical</subject><subject>Quartz Crystal Microbalance Techniques</subject><subject>Quartz crystals</subject><subject>Reflectivity</subject><subject>Saponins</subject><subject>Thermodynamics</subject><issn>1520-6106</issn><issn>1520-5207</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkT9PwzAQxS0EoqUw8AWQFyQYAraTXJoRlX-VqBgKc-Q45-IqsUucgPj2uLR0QmKwfPf009PdO0JOObviTPDr5SplWZLH-R4Z8lSwKLxsf1sDZzAgR94vGROpGMMhGYg04UIwGBI9Q_UmrfGdUXRqPzAUC9kZZ6nTQeiwlWrdelpi94lo6TxozlSypnO5ctZYemsWpvuppK3oBOuazrApW2mRzlyFtT8mB1rWHk-2_4i83t-9TB6jp-eH6eTmKZIJT7oojVWZAsi4SlCBZJAnME51qZkGoSuWa8EkJjJoWZazGBA0co0SAHml83hELja-q9a992GZojFehYHCKK73Bc8grC1igP9RiPOQacLigF5uUNU671vUxao1jWy_Cs6K9QWK3QUCe7a17csGqx35G3kAzjeAVL5Yur61IZA_jL4BmL-NFA</recordid><startdate>20141218</startdate><enddate>20141218</enddate><creator>Frenkel, Nataliya</creator><creator>Makky, Ali</creator><creator>Sudji, Ikhwan Resmala</creator><creator>Wink, Michael</creator><creator>Tanaka, Motomu</creator><general>American Chemical Society</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>7SR</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>L7M</scope></search><sort><creationdate>20141218</creationdate><title>Mechanistic Investigation of Interactions between Steroidal Saponin Digitonin and Cell Membrane Models</title><author>Frenkel, Nataliya ; Makky, Ali ; Sudji, Ikhwan Resmala ; Wink, Michael ; Tanaka, Motomu</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a414t-53cb566a3d4ec6a0694685fbf0f62fd09f20ae4a85f779036e6fe1fea66e1df93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Calorimetry, Differential Scanning</topic><topic>Cell Membrane - chemistry</topic><topic>Cell Membrane - metabolism</topic><topic>Cholesterol</topic><topic>Cholesterol - chemistry</topic><topic>Cholesterol - metabolism</topic><topic>Density</topic><topic>Differential scanning calorimetry</topic><topic>Digitonin - chemistry</topic><topic>Digitonin - metabolism</topic><topic>Interferometry - methods</topic><topic>Membranes</topic><topic>Microbalances</topic><topic>Models, Chemical</topic><topic>Quartz Crystal Microbalance Techniques</topic><topic>Quartz crystals</topic><topic>Reflectivity</topic><topic>Saponins</topic><topic>Thermodynamics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Frenkel, Nataliya</creatorcontrib><creatorcontrib>Makky, Ali</creatorcontrib><creatorcontrib>Sudji, Ikhwan Resmala</creatorcontrib><creatorcontrib>Wink, Michael</creatorcontrib><creatorcontrib>Tanaka, Motomu</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Engineered Materials Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>The journal of physical chemistry. 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In the present work, the interaction mechanism between digitonin and cell membrane models has quantitatively been investigated using a combination of physical techniques. It has been demonstrated that digitonin molecules bind specifically to cholesterol in the membrane, resulting in the formation of cholesterol–digitonin complexes on the membrane surface by removing cholesterol from the membrane core. Changes in the mass density and the film mechanics caused by the digitonin were determined by using quartz crystal microbalance with dissipation (QCM-D), and the combination of X-ray reflectivity (XRR) and dual polarization interferometry (DPI) yielded the hydration level of the cholesterol–digitonin complexes. From differential scanning calorimetry (DSC) analysis, supporting evidence was obtained that cholesterol was removed from the membrane core.</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>25412206</pmid><doi>10.1021/jp5074939</doi><tpages>8</tpages></addata></record> |
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subjects | Calorimetry, Differential Scanning Cell Membrane - chemistry Cell Membrane - metabolism Cholesterol Cholesterol - chemistry Cholesterol - metabolism Density Differential scanning calorimetry Digitonin - chemistry Digitonin - metabolism Interferometry - methods Membranes Microbalances Models, Chemical Quartz Crystal Microbalance Techniques Quartz crystals Reflectivity Saponins Thermodynamics |
title | Mechanistic Investigation of Interactions between Steroidal Saponin Digitonin and Cell Membrane Models |
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