An analysis of interactions between three structurally diverse anthocyanidins, as well as their glucosides, and model biological membranes, albumin, and plasmid DNA
Jazyk angličtina Země Velká Británie, Anglie Médium electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
37558717
PubMed Central
PMC10412636
DOI
10.1038/s41598-023-39470-2
PII: 10.1038/s41598-023-39470-2
Knihovny.cz E-zdroje
- MeSH
- anthokyaniny * metabolismus MeSH
- DNA MeSH
- erytrocytární membrána metabolismus MeSH
- glukosidy * farmakologie chemie MeSH
- lidé MeSH
- lidský sérový albumin MeSH
- plazmidy genetika MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- anthokyaniny * MeSH
- DNA MeSH
- glukosidy * MeSH
- lidský sérový albumin MeSH
The aim of the study is to investigate the differences in the interaction of three structurally diverse anthocyanidins, namely peonidin, petunidin, and delphinidin, as well as their glucosides with model biological membranes, human albumin, and plasmid DNA in order to look into their structure-activity relationships. Fluorimetric studies, as well as ATR-FTIR analyses, were jointly used in order to determine the changes observed in both the hydrophilic and hydrophobic layers of cell-mimic membranes (MM) which reflected the membrane lipid composition of tumour cells and red blood cell membranes (RBCM). Our results showed that anthocyanins and anthocyanidins can cause an increase in the packing order of the polar heads of lipids, as well as interact with their deeper layers by reducing the fluidity of lipid chains. The results presented here indicate that all compounds tested here possessed the ability to bind to human serum albumin (HSA) and the presence of a glucose molecule within the structures formed by anthocyanidin reduces their ability to bind to proteins. Using fluorescence correlation spectroscopy, it was demonstrated that the compounds tested here were capable of forming stable complexes with plasmid DNA and, particularly, strong DNA conformational changes were observed in the presence of petunidin and corresponding glucoside, as well as delphinidin. The results we obtained can be useful in comprehending the anthocyanins therapeutic action as molecular antioxidants and provide a valuable insight into their mechanism of action.
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Chen J, Xu B, Sun J, Jiang X, Bai W. Anthocyanin supplement as a dietary strategy in cancer prevention and management: A comprehensive review. Crit. Rev. Food Sci. Nutr. 2021;0:1–13. PubMed
Li D, Zhang Y, Liu Y, Sun R, Xia M. Purified anthocyanin supplementation reduces dyslipidemia, enhances antioxidant capacity, and prevents insulin resistance in diabetic patients. J. Nutr. 2015;145:742–748. PubMed
Celik E, Sanlier N. Effects of nutrient and bioactive food components on Alzheimer’s disease and epigenetic. Crit. Rev. Food Sci. Nutr. 2019;59:102–113. PubMed
Li D, Wang P, Luo Y, Zhao M, Chen F. Health benefits of anthocyanins and molecular mechanisms: Update from recent decade. Crit. Rev. Food Sci. Nutr. 2017;57:1729–1741. PubMed
Liu J, et al. Anthocyanins: Promising natural products with diverse pharmacological activities. Molecules. 2021;26:1–23. PubMed PMC
Alam MA, et al. Potential health benefits of anthocyanins in oxidative stress related disorders. Phytochem. Rev. 2021;20:705–749.
Rice-Evans CA, Miller NJ, Paganga G. Structure–antioxidant activity relationships of flavonoids and phenolic acids. Free Radic. Biol. Med. 1996;20:933–956. PubMed
Liu H, et al. Current advances in anthocyanins: Structure, bioactivity and human health. J. Food Nutr. Res. 2021;60:203–216.
Huang W, Zhu Y, Li C, Sui Z, Min W. Effect of blueberry anthocyanins malvidin and glycosides on the antioxidant properties in endothelial cells. Oxidative Med. Cell. Longev. 2016;2016:1591803. PubMed PMC
Brown JE, Kelly MF. Inhibition of lipid peroxidation by anthocyanins, anthocyanidins and their phenolic degradation products. Eur. J. Lipid Sci. Technol. 2007;109:66–71.
Erlejman AG, Verstraeten SV, Fraga CG, Oteiza PI. The interaction of flavonoids with membranes: Potential determinant of flavonoid antioxidant effects. Free Radic. Res. 2004;38:1311–1320. PubMed
Laura PF, Garzón MT, Vicente M. Relationship between the antioxidant capacity and effect of rosemary (Rosmarinus officinalis L.) polyphenols on membrane phospholipid order. J. Agric. Food Chem. 2010;58:161–171. PubMed
Mistry T, Cai Y, Lilley T, Haslam E. Polyphenol interactions. Part 5.’ Anthocyanin co-pigmentation. J. Chem. Soc. Perkin Trans. 1991;2(2):1287–1295.
Jaldappagari S, Motohashi N, Gangeenahalli MP, Naismith JH. Bioactive mechanism of interaction between anthocyanins and macromolecules like DNA and proteins. Bioact. Heterocycl. VI. 2008 doi: 10.1007/7081_2008_124. DOI
Sarma AD, Sharma R. Anthocyanin-DNA copigmentation complex: Mutual protection against oxidative damage. Phytochemistry. 1999;52:1313–1318.
Bernhardt I, Ellory JC. Red Cell Membrane Transport in Health and Disease. Berlin/Heidelberg, Germany: Springer Science & Business Media; 2013.
Scheidt HA, Pampel A, Nissler L, Gebhardt R, Huster D. Investigation of the membrane localization and distribution of flavonoids by high-resolution magic angle spinning NMR spectroscopy. Biochim. Biophys. Acta Biomembr. 2004;1663:97–107. PubMed
Tsuchiya H. Structure-dependent membrane interaction of flavonoids associated with their bioactivity. Food Chem. 2010;120:1089–1096.
Arora A, Byrem TM, Nair MG, Strasburg GM. Modulation of liposomal membrane fluidity by flavonoids and isoflavonoids. Arch. Biochem. Biophys. 2000;373:102–109. PubMed
Cyboran-Mikołajczyk S, Jurkiewicz P, Hof M, Kleszczyńska H. The impact of O-glycosylation on cyanidin interaction with POPC membranes: Structure–activity relationship. Molecules. 2018;23:2771. PubMed PMC
Tsuchiya H. Effects of red wine flavonoid components on biomembranes and cell proliferation. Int. J. Wine Res. 2011;3:9–17.
Van Dijk C, Driessen AJM, Recourt K. The uncoupling efficiency and affinity of flavonoids for vesicles. Biochem. Pharmacol. 2000;60:1593–1600. PubMed
Struga P, Spiegel M, Hurynowicz K, Gabrielska J. Interference of malvidin and its mono- and di-glucosides on the membrane—Combined in vitro and computational chemistry study. J. Funct. Foods. 2022;99:105340.
Sok M, Šentjurc M, Schara M. Membrane fluidity characteristics of human lung cancer. Cancer Lett. 1999;139:215–220. PubMed
Kojima K. Molecular aspects of the plasma membrane in tumor cells. Nagoya J. Med. Sci. 1993;56:1–18. PubMed
van Blitterswijk WJ, de Veer G, Krol JH, Emmelot P. Comparative lipid analysis of purified plasma membranes and shed extracellular membrane vesicles from normal murine thymocytes and leukemic GRSL cells. BBA Biomembranes. 1982;688:495–504. PubMed
Dudek A, Spiegel M, Strugała-Danak P, Gabrielska J. Analytical and theoretical studies of antioxidant properties of chosen anthocyanins: A structure–dependent relationships. Int. J. Mol. Sci. 2022;23:5432. PubMed PMC
Rahman MM, Ichiyanagi T, Komiyama T, Hatano Y, Konishi T. Superoxide radical- and peroxynitrite-scavenging activity of anthocyanins; structure–activity relationship and their synergism. Free Radic. Res. 2006;40:993–1002. PubMed
Fukumoto LR, Mazza G. Assessing antioxidant and prooxidant activities of phenolic compounds. J. Agric. Food Chem. 2000;48:3597–3604. PubMed
Tammela P, et al. Permeability characteristics and membrane affinity of flavonoids and alkyl gallates in Caco-2 cells and in phospholipid vesicles. Arch. Biochem. Biophys. 2004;425:193–199. PubMed
Khoo HE, Azlan A, Tang ST, Lim SM. Anthocyanidins and anthocyanins: Colored pigments as food, pharmaceutical ingredients, and the potential health benefits. Food Nutr. Res. 2017;61:1361779. PubMed PMC
Lang Y, et al. Protective effects of bovine serum albumin on blueberry anthocyanins under illumination conditions and their mechanism analysis. Food Res. Int. 2019;122:487–495. PubMed
Xiao J, Cao H, Wang Y, Zhao J, Wei X. Glycosylation of dietary flavonoids decreases the affinities for plasma protein. J. Agric. Food Chem. 2009;57:6642–6648. PubMed
Tang L, Zuo H, Shu L. Comparison of the interaction between three anthocyanins and human serum albumins by spectroscopy. J. Lumin. 2014;153:54–63.
Cahyana Y, Gordon MH. Interaction of anthocyanins with human serum albumin: Influence of pH and chemical structure on binding. Food Chem. 2013;141:2278–2285. PubMed
Zhang J, et al. Structure–affinity relationship of dietary anthocyanin–HSA interaction. J. Berry Res. 2018;8:1–9.
Adjimatera N, Kral T, Hof M, Blagbrough IS. Lipopolyamine-mediated single nanoparticle formation of calf thymus DNA analyzed by fluorescence correlation spectroscopy. Pharm. Res. 2006;23:1564–1573. PubMed
Kanakis CD, Tarantilis PA, Polissiou MG, Diamantoglou S, Tajmir-Riahi HA. Dna interaction with naturally occurring antioxidant flavonoids quercetin, kaempferol, and delphinidin. J. Biomol. Struct. Dyn. 2005;22:719–724. PubMed
Dragan AI, et al. Characterization of PicoGreen interaction with dsDNA and the origin of its fluorescence enhancement upon binding. Biophys. J. 2010;99:3010–3019. PubMed PMC
Wang Y, Schellenberg H, Walhorn V, Toensing K, Anselmetti D. Binding mechanism of PicoGreen to DNA characterized by magnetic tweezers and fluorescence spectroscopy. Eur. Biophys. J. 2017;46:561–566. PubMed
Strugała P, Dudra A, Gabrielska J. Interaction between mimic lipid membranes and acylated and nonacylated cyanidin and its bioactivity. J. Agric. Food Chem. 2016;64:7414–7422. PubMed
Dodge JT, Mitchell C, Hanahan DJ. The preparation and chemical characteristics of hemoglobin-free ghosts of human erythrocytes. Arch. Biochem. Biophys. 1963;100:119–130. PubMed
Włoch A, et al. Interaction of 4′-methylflavonoids with biological membranes, liposomes, and human albumin. Sci. Rep. 2021;11:1–14. PubMed PMC
Alay M, et al. Spectroscopic analysis of the interaction of a peptide sequence of hepatitis G virus with bilayers. Talanta. 2003;60:269–277. PubMed
Engelke M, Bojarski P, Bloß R, Diehl H. Tamoxifen perturbs lipid bilayer order and permeability: Comparison of DSC, fluorescence anisotropy, Laurdan generalized polarization and carboxyfluorescein leakage studies. Biophys. Chem. 2001;90:157–173. PubMed
Selvaraj S, Krishnaswamy S, Devashya V, Sethuraman S, Krishnan UM. Influence of membrane lipid composition on flavonoid-membrane interactions: Implications on their biological activity. Prog. Lipid Res. 2015;58:1–13. PubMed
Lakowicz JR. Principles of Fluorescence Spectroscopy. Plenum Press; 2006.
Verkman A. The quenching of an intermembrane fluorescent probe. A method to study the binding and permeation of phloretin through bilayers. Biochem. Pharmacol. 1980;599:370–379. PubMed
Pruchnik H, et al. Effect of distigmasterol-modified acylglycerols on the fluidity and phase transition of lipid model membranes. Membranes. 2022;12:1054. PubMed PMC
Strugała P, Tronina T, Huszcza E, Gabrielska J. Bioactivity in vitro of quercetin glycoside obtained in Beauveria bassiana culture and its interaction with liposome membranes. Molecules. 2017;22:1520. PubMed PMC
Trnková L, Boušová I, Staňková V, Dršata J. Study on the interaction of catechins with human serum albumin using spectroscopic and electrophoretic techniques. J. Mol. Struct. 2011;985:243–250.
Kral T, Widerak K, Langner M, Hof M. Propidium iodide and PicoGreen as dyes for the DNA fluorescence correlation spectroscopy measurements. J. Fluoresc. 2005;15:179–183. PubMed
Humpolíčková J, et al. Equilibrium dynamics of spermine-induced plasmid DNA condensation revealed by fluorescence lifetime correlation spectroscopy. Biophys. J. 2008;94:17–19. PubMed PMC