Comparative electrokinetic properties of extracellular vesicles produced by yeast and bacteria
Extracellular vesicles (EVs) are nano-sized, biocolloidal proteoliposomes that have been shown to be produced by all cell types studied to date and are ubiquitous in the environment. Extensive literature on colloidal particles has demonstrated the implications of surface chemistry on transport behav...
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Published in | Colloids and surfaces, B, Biointerfaces Vol. 225; p. 113249 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Netherlands
Elsevier B.V
01.05.2023
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Abstract | Extracellular vesicles (EVs) are nano-sized, biocolloidal proteoliposomes that have been shown to be produced by all cell types studied to date and are ubiquitous in the environment. Extensive literature on colloidal particles has demonstrated the implications of surface chemistry on transport behavior. Hence, one may anticipate that physicochemical properties of EVs, particularly surface charge-associated properties, may influence EV transport and specificity of interactions with surfaces. Here we compare the surface chemistry of EVs as expressed by zeta potential (calculated from electrophoretic mobility measurements). The zeta potentials of EVs produced by Pseudomonas fluorescens, Staphylococcus aureus, and Saccharomyces cerevisiae were largely unaffected by changes in ionic strength and electrolyte type, but were affected by changes in pH. The addition of humic acid altered the calculated zeta potential of the EVs, especially for those from S. cerevisiae. Differences in zeta potential were compared between EVs and their respective parent cell with no consistent trend emerging; however, significant differences were discovered between the different cell types and their EVs. These findings imply that, while EV surface charge (as estimated from zeta potential) is relatively insensitive to the evaluated environmental conditions, EVs from different organisms can differ regarding which conditions will cause colloidal instability.
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•EVs produced by Pseudomonas fluorescens, Staphylococcus aureus, and Saccharomyces cerevisiae.•EV zeta potential largely unaffected by changes in ionic strength/electrolyte type.•EV zeta potential affected by changes in pH.•S. cerevisiae EVs affected by presence of humic acid.•No consistent trend for relationship between EV and corresponding parent cell. |
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AbstractList | Extracellular vesicles (EVs) are nano-sized, biocolloidal proteoliposomes that have been shown to be produced by all cell types studied to date and are ubiquitous in the environment. Extensive literature on colloidal particles has demonstrated the implications of surface chemistry on transport behavior. Hence, one may anticipate that physicochemical properties of EVs, particularly surface charge-associated properties, may influence EV transport and specificity of interactions with surfaces. Here we compare the surface chemistry of EVs as expressed by zeta potential (calculated from electrophoretic mobility measurements). The zeta potentials of EVs produced by Pseudomonas fluorescens, Staphylococcus aureus, and Saccharomyces cerevisiae were largely unaffected by changes in ionic strength and electrolyte type, but were affected by changes in pH. The addition of humic acid altered the calculated zeta potential of the EVs, especially for those from S. cerevisiae. Differences in zeta potential were compared between EVs and their respective parent cell with no consistent trend emerging; however, significant differences were discovered between the different cell types and their EVs. These findings imply that, while EV surface charge (as estimated from zeta potential) is relatively insensitive to the evaluated environmental conditions, EVs from different organisms can differ regarding which conditions will cause colloidal instability. Extracellular vesicles (EVs) are nano-sized, biocolloidal proteoliposomes that have been shown to be produced by all cell types studied to date and are ubiquitous in the environment. Extensive literature on colloidal particles has demonstrated the implications of surface chemistry on transport behavior. Hence, one may anticipate that physicochemical properties of EVs, particularly surface charge-associated properties, may influence EV transport and specificity of interactions with surfaces. Here we compare the surface chemistry of EVs as expressed by zeta potential (calculated from electrophoretic mobility measurements). The zeta potentials of EVs produced by Pseudomonas fluorescens, Staphylococcus aureus, and Saccharomyces cerevisiae were largely unaffected by changes in ionic strength and electrolyte type, but were affected by changes in pH. The addition of humic acid altered the calculated zeta potential of the EVs, especially for those from S. cerevisiae. Differences in zeta potential were compared between EVs and their respective parent cell with no consistent trend emerging; however, significant differences were discovered between the different cell types and their EVs. These findings imply that, while EV surface charge (as estimated from zeta potential) is relatively insensitive to the evaluated environmental conditions, EVs from different organisms can differ regarding which conditions will cause colloidal instability. [Display omitted] •EVs produced by Pseudomonas fluorescens, Staphylococcus aureus, and Saccharomyces cerevisiae.•EV zeta potential largely unaffected by changes in ionic strength/electrolyte type.•EV zeta potential affected by changes in pH.•S. cerevisiae EVs affected by presence of humic acid.•No consistent trend for relationship between EV and corresponding parent cell. Extracellular vesicles (EVs) are nano-sized, biocolloidal proteoliposomes that have been shown to be produced by all cell types studied to date and are ubiquitous in the environment. Extensive literature on colloidal particles has demonstrated the implications of surface chemistry on transport behavior. Hence, one may anticipate that physicochemical properties of EVs, particularly surface charge-associated properties, may influence EV transport and specificity of interactions with surfaces. Here we compare the surface chemistry of EVs as expressed by zeta potential (calculated from electrophoretic mobility measurements). The zeta potentials of EVs produced by Pseudomonas fluorescens, Staphylococcus aureus, and Saccharomyces cerevisiae were largely unaffected by changes in ionic strength and electrolyte type, but were affected by changes in pH. The addition of humic acid altered the calculated zeta potential of the EVs, especially for those from S. cerevisiae. Differences in zeta potential were compared between EVs and their respective parent cell with no consistent trend emerging; however, significant differences were discovered between the different cell types and their EVs. These findings imply that, while EV surface charge (as estimated from zeta potential) is relatively insensitive to the evaluated environmental conditions, EVs from different organisms can differ regarding which conditions will cause colloidal instability. |
ArticleNumber | 113249 |
Author | Kuehn, Meta J. McCumber, Alexander W. Dittmer, Dirk P. Hendren, Christine Ogilvie McMillan, Hannah M. Wiesner, Mark R. Rogers, Nicholas M.K. McNamara, Ryan P. |
AuthorAffiliation | g Department of Geological and Environmental Sciences, Appalachian State University, Boone, NC, USA c Department of Civil & Environmental Engineering, Duke University, Durham, NC, USA h Research Institute for Environment, Energy and Economics, Appalachian State University, Boone, NC, USA d Department of Biochemistry, Duke University, Durham, NC, USA b Porter School of Earth and Environmental Studies, Tel Aviv University, Tel Aviv, 69978, Israel e Department of Molecular Genetics and Microbiology, Duke University, Durham, NC, USA j Department of Environmental Sciences and Engineering, University of North Carolina Chapel Hill, Chapel Hill, NC, USA k Department of Microbiology and Immunology, University of North Carolina Chapel Hill, Chapel Hill, NC, USA a Department of Mechanical Engineering, Tel Aviv University, Tel Aviv, 69978, Israel f Center for the Environmental Implications of Nanotechnology, Duke University, Durham, NC, USA |
AuthorAffiliation_xml | – name: g Department of Geological and Environmental Sciences, Appalachian State University, Boone, NC, USA – name: b Porter School of Earth and Environmental Studies, Tel Aviv University, Tel Aviv, 69978, Israel – name: h Research Institute for Environment, Energy and Economics, Appalachian State University, Boone, NC, USA – name: k Department of Microbiology and Immunology, University of North Carolina Chapel Hill, Chapel Hill, NC, USA – name: f Center for the Environmental Implications of Nanotechnology, Duke University, Durham, NC, USA – name: a Department of Mechanical Engineering, Tel Aviv University, Tel Aviv, 69978, Israel – name: e Department of Molecular Genetics and Microbiology, Duke University, Durham, NC, USA – name: c Department of Civil & Environmental Engineering, Duke University, Durham, NC, USA – name: d Department of Biochemistry, Duke University, Durham, NC, USA – name: j Department of Environmental Sciences and Engineering, University of North Carolina Chapel Hill, Chapel Hill, NC, USA |
Author_xml | – sequence: 1 givenname: Nicholas M.K. surname: Rogers fullname: Rogers, Nicholas M.K. email: nmkrogers093@tauex.tau.ac.il organization: Department of Mechanical Engineering, Tel Aviv University, Tel Aviv 69978, Israel – sequence: 2 givenname: Alexander W. surname: McCumber fullname: McCumber, Alexander W. organization: Department of Environmental Sciences and Engineering, University of North Carolina Chapel Hill, Chapel Hill, NC, USA – sequence: 3 givenname: Hannah M. surname: McMillan fullname: McMillan, Hannah M. organization: Department of Molecular Genetics and Microbiology, Duke University, Durham, NC, USA – sequence: 4 givenname: Ryan P. surname: McNamara fullname: McNamara, Ryan P. organization: Department of Microbiology and Immunology, University of North Carolina Chapel Hill, Chapel Hill, NC, USA – sequence: 5 givenname: Dirk P. surname: Dittmer fullname: Dittmer, Dirk P. organization: Department of Microbiology and Immunology, University of North Carolina Chapel Hill, Chapel Hill, NC, USA – sequence: 6 givenname: Meta J. surname: Kuehn fullname: Kuehn, Meta J. organization: Department of Biochemistry, Duke University, Durham, NC, USA – sequence: 7 givenname: Christine Ogilvie surname: Hendren fullname: Hendren, Christine Ogilvie organization: Center for the Environmental Implications of Nanotechnology, Duke University, Durham, NC, USA – sequence: 8 givenname: Mark R. surname: Wiesner fullname: Wiesner, Mark R. organization: Department of Civil & Environmental Engineering, Duke University, Durham, NC, USA |
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Keywords | Yeast Colloidal stability Zeta potential Environmental fate Bacteria Extracellular vesicle Surface potential |
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SubjectTerms | Bacteria Colloidal stability Environmental fate Extracellular vesicle Extracellular Vesicles - chemistry Saccharomyces cerevisiae Surface potential Yeast Zeta potential |
Title | Comparative electrokinetic properties of extracellular vesicles produced by yeast and bacteria |
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