BIOPHYSICAL AND IMMUNOLOGICAL CHARACTERIZATION OF CARBAMYLATED-DNA: SERUM AUTOANTIBODIES OF DIABETIC NEPHROPATHY PATIENTS EXHIBIT STRONG BINDING WITH CARBAMYLATED-DNA

Authors

  • M Arif Iqubal Department of Biochemistry, Jawaharlal Nehru Medical College, Faculty of Medicine, Aligarh Muslim University, Aligarh – 202 002, Uttar Pradesh (India)
  • Zarina Arif Department of Biochemistry, Jawaharlal Nehru Medical College, Faculty of Medicine, Aligarh Muslim University, Aligarh – 202 002, Uttar Pradesh (India)
  • Asim Badar Department of Biochemistry, Jawaharlal Nehru Medical College, Faculty of Medicine, Aligarh Muslim University, Aligarh – 202 002, Uttar Pradesh (India)
  • Khursheed Alam Department of Biochemistry, Jawaharlal Nehru Medical College, Faculty of Medicine, Aligarh Muslim University, Aligarh – 202 002, Uttar Pradesh (India)

DOI:

https://doi.org/10.48165/

Keywords:

Autoantibodies, carbamylated-DNA, diabetic nephropathy, isocyanates

Abstract

Isocyanates (ICN) have drawn considerable attention in recent past as they  can react with a variety of nucleophiles including DNA, proteins and cause  damage(s). However, pathophysiological implications resulting from the  occupational and accidental exposures of ICN are yet too elusive. It may be  produced in high concentrations in the conditions of chronic renal failure  and chronic inflammatory diseases (diabetes mellitus, rheumatoid  arthritis, etc.). In this study, mammalian dsDNA was modified with ICN  and characterized by UV, fluorescence, FT-IR and thermal melting methods. ICN mainly reacts with exocyclic nitrogen of DNA bases.  Antibodies against carbamylated-DNA were raised in rabbits and  characterized by direct binding and inhibition ELISA. The presence of  anti-carbamylated-DNA autoantibodies in the sera of diabetic nephro pathy patients was evaluated by ELISA. Carbamylated-DNA exhibited  hyperchromicity at 260 nm and depicted increase in ethidium bromide assisted fluorescence as compared to the native DNA. Furthermore, the appearance of prominent new peaks in FT-IR profile at different wave  numbers suggested carbamoylation-induced changes in the vibration of  sugar-phosphate backbone, base(s) etc. Carbamylated-DNA was highly  immunogenic as compared to the native DNA. Experimental induction of  antibodies against carbamylated-DNAand presence of autoantibodies  against carbamylated-DNA in the sera of diabetic nephropathic patients  point towards the significance of carbamylated-DNA in diabetic  nephropathy. 

Downloads

Download data is not yet available.

References

Ahmad, S., Uddin, M., Habib, S., Shahab, U., Alam, K. and Ali, A. 2014. Autoimmune response to AGE modified human DNA: Implications in type 1 Diabetes mellitus. Journal of Clinical and Translational Endocrinology, 1: 66-72.

Alam, K. and Jabeen, S. 2007. Immunogenicity of mitochondrial DNA modified by hydroxyl radical. Cellular Immunology, 247: 12-17.

Alam, K., Ali, A. and Ali, R. 1993. The effect of hydroxyl radical on the antigenicity of native DNA. FEBS Letters, 319: 66-70.

Baumann, R.P., Seow, H.A., Shyam, K., Penketh, P.G. and Sartorelli, A.C. 2005. The antineoplastic efficacy of the prodrug Cloretazine TM is produced by the synergistic interaction of carbamoylating and alkylating products of its activation. Oncology Research Featuring Preclinical and Clinical Cancer Therapeutics, 15: 313-325.

Benigni, R. and Bossa, C. 2011. Mechanisms of chemical carcinogenicity and mutagenicity: a review with implications for predictive toxicology. Chemical Reviews, 111: 2507-2536. Beyerbach, A., Farmer, P.B. and Sabbioni, G. 2006. Biomarkers for isocyanate exposure: Synthesis of isocyanate DNA adducts. Chemical Research in Toxicology, 19: 1611-1618. Caspary, W.J. and Myhr, B. 1986. Mutagenicity of methylisocyanate and its reaction products to cultured mammalian cells. Mutation Research Letters, 174: 285-293.

Chen, C.N., Porubleva, L., Shearer, G., Svrakic, M., Holden, L.G., Dover, J.L., Johnston, M., Chitnis, P.R. and Kohl, D.H. 2003. Associating protein activities with their genes: rapid identification of a gene encoding a methylglyoxal reductase in the yeast Saccharomyces cerevisiae. Yeast, 20: 545-554.

Delanghe, S., Delanghe, J.R., Speeckaert, R., Van Biesen, W. and Speeckaert, M.M. 2017. Mechanisms and consequences of carbamoylation. Nature Reviews Nephrology, 13: 580-593.

Carbamylated-DNA autoantibodies in diabetic nephropathy 325

Deo, M.G., Gangal, S., Bhisey, A., Somasundaram, R., Balsara, B., Gulwani, B., Darbari, B.S., Bhide, S. and Maru, G.B. 1987. Immunological, mutagenic and genotoxic investigations in gas exposed population of Bhopal. Indian Journal of Medical Research, 86: 63-76.

Dovbeshko, G.I., Gridina, N.Y., Kruglova, E.B. and Pashchuk, O.P. 2000. FTIR spectroscopy studies of nucleic acid damage. Talanta, 53: 233-246.

East, C.J., Abboud, C.N. and Borch, R.F. 1992. Diethyldithiocarbamate induction of cytokine release in human long-term bone marrow cultures. Blood, 80: 1172-117,

Heath, R. 2017. Isocyanate-based polymers: polyurethanes, polyureas, polyisocyanurates, and their copolymers. pp. 799-835. In: Brydson’s Plastics Materials 8th edn. (ed. M. Gilbert). Elsevier, Oxford, UK.

Hu, R., Kim, B.R., Chen, C., Hebbar, V. and Kong, A.N.T.2003. The roles of JNK and apoptotic signalling pathways in PEITC-mediated responses in human HT-29 colon adenocarcinoma cells. Carcinogenesis, 24: 1361-1367.

Liljenberg, M., Ripa, L. and Shamovsky, I. 2020. Theoretical Studies of the Mechanism of Carbamoylation of Nucleobases by Isocyanates. Chemical Research in Toxicology, 33: 2845- 2853.

Marczynski, G.T. and Shapiro, L. 1992. Cell-cycle control of a cloned chromosomal origin of replication from Caulobacter crescentus. Journal of Molecular Biology, 226: 959-977. Mishra, P.K., Panwar, H., Bhargava, A., Gorantla, V.R., Jain, S.K., Banerjee, S. and Maudar, K.K., 2008. Isocyanates induces DNA damage, apoptosis, oxidative stress, and inflammation in cultured human lymphocytes. Journal of Biochemical and Molecular Toxicology, 22: 429-440. Pijanka, J.K., Kohler, A., Yang, Y., Dumas, P., Chio-Srichan, S., Manfait, M., Sockalingum, G.D. and Sulé-Suso, J. 2009. Spectroscopic signatures of single, isolated cancer cell nuclei using synchrotron infrared microscopy. Analyst, 134: 1176-1181.

Polak, W., Lekki, J., Veselov, O., Stachura, Z. and Styczen, J. 2006. Single proton hit facility at the IFJ PAN in Cracow. Acta Physica Polonica - Series A General Physics, 109: 417-420. Saxena, A.K., Singh, K.P., Nagle, S.L., Gupta, B.N., Ray, P., Srivastav, R.K., Tewari, S.P. and Singh, R. 1988. Effect of exposure to toxic gas on the population of Bhopal: Part IV-- Immunological and chromosomal studies. Indian Journal of Experimental Biology, 26: 173- 176.

Segal, A., Solomon, J.J. and Li, F. 1989. Isolation of methylcarbamoyl-adducts of adenine and cytosine following in vitro reaction of methyl isocyanate with calf thymus DNA. Chemico Biological Interactions, 69: 359-372.

Shelby, M.D., Allen, J.W., Caspary, W.J., Haworth, S., Ivett, J., Kligerman, A., Luke, C.A., Mason, J.M., Myhr, B., Tice, R.R. and Valencia, R. 1987. Results of in vitro and in vivo genetic toxicity tests on methyl isocyanate. Environmental Health Perspectives, 72: 183-187.

Smith, G.F. 2011. Designing drugs to avoid toxicity. Progress in Medicinal Chemistry, 50: 1-47. Talha, M., Mir, A.R., Habib, S., Abidi, M., Warsi, M.S. and Islam, S. 2021. Hydroxyl radical induced structural perturbations make insulin highly immunogenic and generate an auto immune response in type 2 diabetes mellitus. Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, 255: 1-14.

Tamura, N., Aoki, K. and Lee, M.S. 1990. Characterization and genotoxicity of DNA adducts caused by 2-naphthyl isocyanate. Carcinogenesis, 11: 2009-2014.

Tamura, N., Aoki, K. and Lee, M.S. 1992. Selective reactivities of isocyanates towards DNA bases and genotoxicity of methyl carbamoylation of DNA. Mutation Research Letters, 283: 97-106. Tang, L. and Zhang, Y. 2005. Mitochondria are the primary target in isothiocyanate-induced apoptosis in human bladder cancer cells. Molecular Cancer Therapeutics, 4: 1250-1259. Tantry, I.Q., Waris, S., Habib, S., Khan, R.H., Mahmood, R. and Ali, A., 2018. Hypochlorous acid induced structural and conformational modifications in human DNA: a multi-spectroscopic study. International Journal of Biological Macromolecules, 106: 551-558.

M. Arif Iqubal et al.

Ugenskiene, R., Lekki, J., Polak, W., Prise, K.M., Folkard, M., Veselov, O., Stachura, Z., Kwiatek, W.M., Zazula, M. and Stachura, J.2007. Double strand break formation as a response to X-ray and targeted proton-irradiation. Nuclear Instruments and Methods in Physics Research Section B: Beam Interactions with Materials and Atoms, 260: 159-163.

Vandenabeele-Trambouze, O., Mion, L., Garrelly, L. and Commeyras, A. 2001. Reactivity of organic isocyanates with nucleophilic compounds: amines; alcohols; thiols; oximes; and phenols in dilute organic solutions. Advances in Environmental Research, 6: 45-55.

Wang, Z. 2009. Comprehensive Organic Name Reactions and Reagents, Hoboken, NJ, John Wiley. Waris, G. and Alam, K. 2004. Immunogenicity of superoxide radical modified-DNA: studies on induced antibodies and SLE anti-DNA autoantibodies. Life Sciences, 75: 2633-2642. Worthy, W.1985. Methyl isocyanate-The chemistry of a hazard. Chemical and Engineering News, 63: 27-33.

Zhang, Y., Tang, L. and Gonzalez, V. 2003. Selected isothiocyanates rapidly induce growth inhibition of cancer cells. Molecular Cancer Therapeutics, 2: 1045-1052.

Published

2023-11-16

How to Cite

BIOPHYSICAL AND IMMUNOLOGICAL CHARACTERIZATION OF CARBAMYLATED-DNA: SERUM AUTOANTIBODIES OF DIABETIC NEPHROPATHY PATIENTS EXHIBIT STRONG BINDING WITH CARBAMYLATED-DNA . (2023). Applied Biological Research, 24(3), 317–326. https://doi.org/10.48165/