Monitoring of the Zeta Potential of Human Cells upon Reduction in Their Viability and Interaction with Polymers
- Authors: Bondar O.V.1, Saifullina D.V.1, Shakhmaeva I.I.1, Mavlyutova I.I.1, Abdullin T.I.1
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Affiliations:
- Kazan (Volga Region) Federal University
- Issue: Vol 4, No 1 (2012)
- Pages: 78-81
- Section: Research Articles
- Submitted: 17.01.2020
- Published: 15.03.2012
- URL: https://actanaturae.ru/2075-8251/article/view/10637
- DOI: https://doi.org/10.32607/20758251-2012-4-1-78-81
- ID: 10637
Cite item
Abstract
The dynamic light scattering (DLS) technique was applied in order to assess the zeta potential of the plasma membrane of human cells. At pH 7.4, the cell zeta potential for different types of cells showed variations over a wide range and was equal to -19.4 ± 0.8 mV for HeLa cells and -31.8 ± 1.1 mV for erythrocytes. The difference could presumably be attributed to the differences in the biochemical composition of the cell plasma membrane. As a result of the heating of HeLa cells, the zeta potential shifted towards more negative voltages by 4.2 mV. An increase in the zeta potential correlated with an increase in the content of phosphatidylserine on the cell surface, which is considered to be an early marker of apoptosis. The DLS technique was also used to study the interactions between the cells and membranotropic polymers, such as polycations and nonionogenic Pluronic L121.
About the authors
O. V. Bondar
Kazan (Volga Region) Federal University
Author for correspondence.
Email: oxanav.bondar@gmail.com
Россия
D. V. Saifullina
Kazan (Volga Region) Federal University
Email: oxanav.bondar@gmail.com
Россия
I. I. Shakhmaeva
Kazan (Volga Region) Federal University
Email: oxanav.bondar@gmail.com
Россия
I. I. Mavlyutova
Kazan (Volga Region) Federal University
Email: oxanav.bondar@gmail.com
Россия
T. I. Abdullin
Kazan (Volga Region) Federal University
Email: oxanav.bondar@gmail.com
Россия
References
- Fernie A.R., Trethewey R.N., Krotzky A.J., Willmitzer L. // Nat. Rev. Mol. Cell. Biol. 2004. V. 5. P. 763-769.
- Boros L.G., Cascante M., Lee W.N. // Drug discovery today. 2002. V. 7. P. 364-372.
- Fang J., Palanisami A., Rajapakshe K. // Biosensors. 2011. V. 1. P 13-22.
- Kuo Y.-C., Lin T.-W. // J. Phys. Chem. B. 2006. V. 110. № 5. P. 2202-2208.
- Wilson W., Wade M., Holman S., Champlin F.R. // J. Microbiol. Meth. 2001. V. 43. P 153-164.
- Eylar E.H., Madoff M.A., Brody O.V., Oncley J.L. // J. Biol. Chem. 1962. V. 237. P. 1992-2000.
- Pack D.W., Hoffman A.S., Stayton S.P., Stayton PS. // Nat. Rev. Drug Disc. 2005. V. 4. P. 581-593.
- Firestone M.A., Wolf A.C., Seifert S. // Biomacromolecules. 2003. V. 4. P 1539-1549.
- Bryskhe K., Schillen K., Loéfroth J.E., Olsson U. // Phys. Chem. Chem. Phys. 2001. V. 3. P. 1303-1309.
- Erukova V.Yu., Krylova O.O., Antonenko Yu.N., Melik-Nubarov N.S. // Biochim. Biophys. Acta. 2000. V. 1468. P. 73-86.