Comparison of the Effects on Bovine Serum Albumin Induced by Different Forms of Vanadium.

Bovine serum albumin Interaction Oxidovanadium(IV) acetylacetonate Oxidovanadium(IV) sulfate Sodium metavanadate Spectroscopic measurements

Journal

Biological trace element research
ISSN: 1559-0720
Titre abrégé: Biol Trace Elem Res
Pays: United States
ID NLM: 7911509

Informations de publication

Date de publication:
Jun 2023
Historique:
received: 31 05 2022
accepted: 26 07 2022
medline: 6 4 2023
pubmed: 2 8 2022
entrez: 1 8 2022
Statut: ppublish

Résumé

Various forms of vanadium coexist in vivo, and the behavior mechanism is different. An investigation of the separate and simultaneous binding of three vanadium forms with bovine serum albumin (BSA) was performed. VO(acac)

Identifiants

pubmed: 35915278
doi: 10.1007/s12011-022-03373-6
pii: 10.1007/s12011-022-03373-6
doi:

Substances chimiques

Serum Albumin, Bovine 27432CM55Q
Vanadium 00J9J9XKDE

Types de publication

Comparative Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

3088-3098

Informations de copyright

© 2022. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.

Références

Lin Q, Xu S, Zhou A, Liu W, Liao J, Cao Z, Chen Z, Yao C, Zhang Y, Li Y (2020) Association between changes in gestational blood pressure and vanadium exposure in China. Environ Toxicol Phar 79:103424. https://doi.org/10.1016/j.etap.2020.103424
doi: 10.1016/j.etap.2020.103424
Awan RS, Liu C, Yang S, Wu Y, Zang Q, Khan A, Li G (2021) The occurrence of vanadium in nature: its biogeochemical cycling and relationship with organic matter-a case study of the early Cambrian black rocks of the niutitang formation, western human. China Acta Geochim 40:1–25. https://doi.org/10.1007/s11631-021-00482-2
doi: 10.1007/s11631-021-00482-2
Omidinasab M, Rahbar N, Ahmadi M, Kakavandi B, Ghanbari F, Kuzas GZ, Martinez SS, Jaafarzadeh N (2018) Removal of vanadium and palladium ions by adsorption onto magnetic chitosan nanoparticles. Environ Sci Pollut Res 25:34262–34276. https://doi.org/10.1007/s11356-018-3137-1
doi: 10.1007/s11356-018-3137-1
Imtiaz M, Rizwan MS, Xiong S, Li H, Ashraf M, Shahzad SM, Shahzard M, Rizwan M, Tu S (2015) Vanadium, recent advancements and research prospects: a review. Environ Int 80:79–88. https://doi.org/10.1016/j.envint.2015.03.018
doi: 10.1016/j.envint.2015.03.018 pubmed: 25898154
Huang JH, Huang F, Evans L, Glasauer S (2015) Vanadium: global (bio) geochemistry. Chem Geol 417:68–89. https://doi.org/10.1016/j.chemgeo.2015.09.019
doi: 10.1016/j.chemgeo.2015.09.019
Yu YQ, Yang JY (2018) Oral bioaccessibility and health risk assessment of vanadium(IV) and vanadium(V) in a vanadium titanomagnetite mining region by a whole digestive system in-vitro method (WDSM). Chmosphere 215:294–304. https://doi.org/10.1016/j.chemosphere.2018.10.042
doi: 10.1016/j.chemosphere.2018.10.042
Rehder D (2015) The role of vanadium in biology. Metallomics 7(5):730–742. https://doi.org/10.1039/C4MT00304G
doi: 10.1039/C4MT00304G pubmed: 25608665
Ngwa HA, Ay M, Jin H, Anantharam V, Kanthasamy A, Kanthasamy AG (2017) Neurotoxicity of vanadium. Adv Neurobiol 18:287–301. https://doi.org/10.1007/978-3-319-60189-2_14
doi: 10.1007/978-3-319-60189-2_14 pubmed: 28889273
Treviño S, Díaz A, Sánchez-Lara E, Sanche-Gaytan BL, Perez-Aguilar JM, Gonzalea-Vegara E (2019) Vanadium in biological action: chemical, pharmacological aspects, and metabolic implications in diabetes mellitus. Biol Trace Elem Res 188:68–98. https://doi.org/10.1007/s12011-018-1540-6
doi: 10.1007/s12011-018-1540-6 pubmed: 30350272
Scibior A, Pietrayk L, Piewa Z, Skiba A (2020) Vanadium: risks and possible benefits in the light of a comprehensive overview of its pharmacotoxicological mechanisms and multi-applications with a summary of further research trends. J Trace Elem Med Bio 61:126508. https://doi.org/10.1016/j.jtemb.2020.126508
doi: 10.1016/j.jtemb.2020.126508
Chiarelli R, Martino C, Roccheri MC, Cancemi P (2021) Toxic effects induced by vanadium on sea urchin embryos. Chemosphere 274:129843. https://doi.org/10.1016/j.chemosphere.2021.129843
doi: 10.1016/j.chemosphere.2021.129843 pubmed: 33561719
Hemmatifar A, Ozbek N, Halliday C, Hatton TA (2020) Electrochemical selective recovery of heavy metal vanadium oxyanion from continuously flowing aqueous streams. Chemsuschem 13(15):3865–3874. https://doi.org/10.1002/cssc.202001094
doi: 10.1002/cssc.202001094
Bishayee A, Waghray A, Patel MA, Chatterjee M (2010) Vanadium in the detection, prevention and treatment of cancer: the in vivo evidence. Cancer Lett 294:1–12. https://doi.org/10.1016/j.canlet.2010.01.030
doi: 10.1016/j.canlet.2010.01.030 pubmed: 20206439
Dias DM, Rodrigues JPGLM, Domigues NS, Bonvin AMJJ, Castro MMCA (2013) Unveiling the Interaction of vanadium compounds with human serum albumin by using
doi: 10.1002/ejic.201300419
Lv X, Jiang Z, Zeng G, Zhao S, Li N, Chen F, Huang X, Yao J, Tuo X (2021) Comprehensive insights into the interactions of dicyclohexyl phthalate and its metabolite to human serum albumin. Food Chem Toxicol 155:112407. https://doi.org/10.1016/j.fct.2021.112407
doi: 10.1016/j.fct.2021.112407 pubmed: 34273427
Sokolowska M, Szelaka-Rylik MW, Poznański J, Bal W (2009) Spectroscopic and thermodynamic determination of three distinct binding sites for Co(II) ions in human serum albumin. J Inorg Biochem 103(7):1005–1013. https://doi.org/10.1016/j.jinorgbio.2009.04.011
doi: 10.1016/j.jinorgbio.2009.04.011 pubmed: 19487034
Pessoa JC, Garribba E, Santos MFA, Santos-Silva T (2015) Vanadium and proteins: uptake, transport, structure, activity and function. Coordin Chem Rev 301–302:49–86. https://doi.org/10.1016/j.ccr.2015.03.016
doi: 10.1016/j.ccr.2015.03.016
Raza M, Ahmad A, Feng Y, Khan Z, Yang J (2017) Biophysical and molecular docking approaches for the investigation of biomolecular interactions between amphotericin B and bovine serum albumin. J Photoch Photobio B 170:6–15. https://doi.org/10.1016/j.jphotobiol.2017.03.014
doi: 10.1016/j.jphotobiol.2017.03.014
Correia I, Jakusch T, Cobbinna E, Mehtab S, Tomaz I, Nagy NV, Rockenbauer A, Pessoa JC, Kiss T (2012) Evaluation of the binding of oxovanadium(IV) to human serum albumin. Dalton Trans 41(21):6477–6487. https://doi.org/10.1039/C2DT12247B
doi: 10.1039/C2DT12247B pubmed: 22476413
Ferrer EG, Bosch A, Yantorno O, Baran EJ (2008) A spectroscopy approach for the study of the interactions of bioactive vanadium species with bovine serum albumin. Bioorgan Med Chem 16(7):3878–3886. https://doi.org/10.1016/j.bmc.2008.01.060
doi: 10.1016/j.bmc.2008.01.060
Purcell M, Neault JF, Malonga H, Arakawa H, Tajmir-Riahi HA (2001) Interaction of human serum albumin with oxovanadium ions studied by FT-IR spectroscopy and gel and capillary electrophoresis. Can J Chem 79:1415–1421. https://doi.org/10.1139/cjc-79-10-1415
doi: 10.1139/cjc-79-10-1415
Sanna D, Garribba E, Micera G (2009) Interaction of VO
doi: 10.1016/j.jinorgbio.2009.01.002 pubmed: 19201482
Sanna D, Micera G, Garribba E (2009) On the transport of vanadium in blood serum. Inorg Chem 48(13):5747–5757. https://doi.org/10.1021/ic802287s
doi: 10.1021/ic802287s pubmed: 19514735
Desaulniers D, Cummings-Lorbetskie C, Leingartner K, Xiao GH, Zhou G (2021) Effects of vanadium (sodium metavanadate) and aflatoxin-B1 on cytochrome p450 activities, DNA damage and DNA methylation in human liver cell lines. Toxicol In Vitro 70:105036. https://doi.org/10.1016/j.tiv.2020.105036
doi: 10.1016/j.tiv.2020.105036 pubmed: 33164849
Wani TA, Bakheit AH, Ansari MN, Al-Majed AA, Al-Qahtani MB, Zargar S (2018) Spectroscopic and molecular modeling studies of binding interaction between bovine serum albumin and roflumilast. Drug Des Dev Ther 12:2627–2634. https://doi.org/10.2147/DDDT.S169697
doi: 10.2147/DDDT.S169697
Sun J, Huang Y, Zheng C, Zhou Y, Liu Y, Liu J (2015) Ruthenium (II) complexes interact with human serum albumin and induce apoptosis of tumor cells. Biol Trace Elem Res 163:266–274. https://doi.org/10.1007/s12011-014-0165-7
doi: 10.1007/s12011-014-0165-7 pubmed: 25398541
Soares FA, Ceschi MA, Franceschini DB, Canto VP, Netz PA, Campo LF (2019) Tianeptine esters derivatives: a study of protein-drug interaction performed by fluorescence quenching and molecular docking. J Brazil Chem Soc 30(10): 2125–2135. https://doi.org/10.21577/0103-5053.20190090
Mariam J, Dongre PM, Kothari DC (2011) Study of interaction of silver nanoparticles with bovine serum albumin using fluorescence spectroscopy. J Fluoresc 21(6):2193–2199. https://doi.org/10.1007/s10895-011-0922-3
doi: 10.1007/s10895-011-0922-3 pubmed: 21773692
Lv Y, Liang Q, Li Y, Liu X, Zhang D, Li X (2022) Study of the binding mechanism between hydroxytyrosol and bovine serum albumin using multispectral and molecular docking. Food Hydrocolloid 122:107072. https://doi.org/10.1016/j.foodhyd.2021.107072
doi: 10.1016/j.foodhyd.2021.107072
Kőszegi T, Poór M (2016) Ochratoxin A: molecular interactions, mechanisms of toxicity and prevention at the molecular level. Toxins 8(4):111. https://doi.org/10.3390/toxins8040111
doi: 10.3390/toxins8040111 pubmed: 27092524 pmcid: 4848637
Farajzadeh-Dehkordi N, Zahraei Z, Farhadian S, Gholamian-Dehkordi N (2022) The interactions between Reactive Black 5 and human serum albumin: combined spectroscopic and molecular dynamics simulation approaches. Enciron Sci Pollut Res. https://doi-org.unimib.80599.net/ https://doi.org/10.1007/s11356-022-20736-7
Huang S, Peng S, Zhu F, Lei X, Xiao Q, Su W, Liu Y, Huang C, Zhang L (2016) Multispectroscopic investigation of the interaction between two ruthenium(II) arene complexes of curcumin analogs and human serum albumin. Biol Trace Elem Res 169(2):189–203. https://doi.org/10.1007/s12011-015-0416-2
doi: 10.1007/s12011-015-0416-2 pubmed: 26170171
Yang J, Huang SC, Wang Y, Ji MY, Hu YJ (2021) Multispectroscopic, electrochemical and molecular docking approaches on binding comparison of camptothecin, 10-hydroxycamptothecin to bovine serum albumin. J Mol Liq 326:115296. https://doi.org/10.1016/j.molliq.2021.115296
doi: 10.1016/j.molliq.2021.115296
Lou YY, Zhou KL, Pan DQ, Shen JL, Shi JH (2017) Spectroscopic and molecular docking approaches for investigating conformation and binding characteristics of clonazepam with bovine serum albumin (BSA). J Photobio B 167:158–167. https://doi.org/10.1016/j.jphotobiol.2016.12.029
doi: 10.1016/j.jphotobiol.2016.12.029
Gadallah MI, Ali HRH, Askal HF, Saleh GA (2021) Towards understanding of the interaction of certain carbapenems with protein via combined experimental and theoretical approach. Spectrochim Acta A 246:119005. https://doi.org/10.1016/j.saa.2020.119005
doi: 10.1016/j.saa.2020.119005
Khatun S, Uddeen R (2018) Probing of the binding profile of anti-hypertensive drug, captopril with bovine serum albumin: a detailed calorimetric, spectroscopic and molecular docking studies. J Chem Thermodyn 126:43–53. https://doi.org/10.1016/j.jct.2018.06.004
doi: 10.1016/j.jct.2018.06.004
Nasiri F, Dehghan G, Shaghaghi M, Datmalchi S, Irashanhi M (2021) Probing the interaction between 7-geranyloxycoumarin and bovine serum albumin: spectroscopic analyzing and molecular docking study. Spectrochim Acta A 254:119664. https://doi.org/10.1016/j.saa.2021.119664
doi: 10.1016/j.saa.2021.119664
Khayyat AIA, Zargar S, Wani TA, Rehman MU, Khan AA (2022) Association mechanism and conformational changes in trypsin on its interaction with atrazine: a multi-spectroscopic and biochemical study with computational approach. Int J Mol Sci 23:5636. https://doi.org/10.3390/ijms23105636
doi: 10.3390/ijms23105636 pubmed: 35628445 pmcid: 9146720
Zargar S, Wani TA (2021) Exploring the binding mechanism and adverse toxic effects of persistent organic pollutant (dicofol) to human serum albumin: a biophysical, biochemical and computational approach. Chem-Biol Interact 350:109707. https://doi.org/10.1016/j.cbi.2021.109707
doi: 10.1016/j.cbi.2021.109707 pubmed: 34656558
Zhang Y, Shi S, Sun X, Huang K, Chen X, Peng M (2011) Structure-affinity relationship of bovine serum albumin with dietary flavonoids with different C-ring substituents in the presence of Fe
doi: 10.1016/j.foodres.2011.06.045
He L, Wang Y, Wu X, Liu X, Wang X, Liu B, Wang X (2015) Enhancement of the binding affinity of methylene blue to site I in human serum albumin by cupric and ferric ions. Luminescence 30(8):1380–1388. https://doi.org/10.1002/bio.2910
doi: 10.1002/bio.2910 pubmed: 25833007
Sun Q, Yang H, Tang P, Liu J, Wang W, Li H (2018) Interactions of cinnamaldehyde and its metabolite cinnamic acid with human serum albumin and interference of other food additives. Food Chem 243:74–81. https://doi.org/10.1016/j.foodchem.2017.09.109
doi: 10.1016/j.foodchem.2017.09.109 pubmed: 29146372

Auteurs

Qionghua Zhang (Q)

College of Chemistry and Chemical Engineering, Bohai University, 19, Keji Rd., New Songshan District, Jinzhou, Liaoning Province, 121013, People's Republic of China.

Yanxuan Ma (Y)

College of Chemistry and Chemical Engineering, Bohai University, 19, Keji Rd., New Songshan District, Jinzhou, Liaoning Province, 121013, People's Republic of China.

Hongrui Liu (H)

College of Chemistry and Chemical Engineering, Bohai University, 19, Keji Rd., New Songshan District, Jinzhou, Liaoning Province, 121013, People's Republic of China.

Jiali Gu (J)

College of Chemistry and Chemical Engineering, Bohai University, 19, Keji Rd., New Songshan District, Jinzhou, Liaoning Province, 121013, People's Republic of China. gujiali_99@163.com.

Xuekai Sun (X)

Institute of Applied Ecology, Chinese Academy of Sciences, Shenyang, 110016, People's Republic of China.

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