Study of the Activation Process of Isotope Exchange between Boc-Trp-Pro-Pro-Trp, Trp-Pro-Pro-Trp and Deuterated Water

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The conditions for introducing deuterium into Trp-Pro-Pro-Trp and Boc-Trp-Pro-Pro-Trp by isotope exchange with D2O in the presence of a 5% Pd/Al2O3 catalyst were developed. The thermal stability of Trp-Pro-Pro-Trp upon introduction of deuterium was significantly lower than that of the Boc-protected peptide. The yield of deuterated Trp-Pro-Pro-Trp did not exceed 10–15%, and the inclusion of deuterium was about 0.9–1.1 at./molecule at 125°C. The introduction of deuterium into Boc-Trp-Pro-Pro-Trp was possible at 150°C, which increased the deuterium content to 3.75 at./molecule. It was found that the tryptophan fragment of the molecule contains approximately 2 times more deuterium than the proline fragment. It was found that pretreatment of Boc-Trp-Pro-Pro-Trp with deuterium gas not only activates isotope exchange, but also promotes the removal of Boc protection. The data obtained indicate that the reason for this phenomenon is associated with the generation of deuterium cations on Boc-Trp-Pro-Pro-Trp molecules by the catalyst.

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作者简介

V. Shevchenko

National Research Centre Kurchatov Institute

编辑信件的主要联系方式.
Email: nagaev.img@yandex.ru
俄罗斯联邦, pl. Kurchatova 2, Moscow, 123182

K. Shevchenko

National Research Centre Kurchatov Institute

Email: nagaev.img@yandex.ru
俄罗斯联邦, pl. Kurchatova 2, Moscow, 123182

I. Nagaev

National Research Centre Kurchatov Institute

Email: nagaev.img@yandex.ru
俄罗斯联邦, pl. Kurchatova 2, Moscow, 123182

L. Andreeva

National Research Centre Kurchatov Institute

Email: nagaev.img@yandex.ru
俄罗斯联邦, pl. Kurchatova 2, Moscow, 123182

参考

  1. Prince M. J., Wimo A., Guerchet M. M., Ali G. C., Wu Y. T., Prina M. World Alzheimer Report 2015—The Global Impact of Dementia: An Analysis of Prevalence, Incidence, cost and Trends. Alzheimer’s Disease International. London. 87 p.
  2. Shevchenko V. P., Nagaev I. Yu., Myasoedov N. F., Susan A. B. // J. Label. Compd. Radiopharm. 2007. Vol. 50. N5–6. C. 416–417. https://doi.org/10.1002/jlcr.1167
  3. Shevchenko V. P., Nagaev I. Yu., Myasoedov N. F. // J. Label. Compd. Radiopharm. 2010. Vol. 53. N11–12. P. 693–703. https://doi.org/10.1002/jlcr.1828
  4. Kopf S., Bourriquen F., Li W., Neumann H., Junge K., Beller M. // Chem. Rev. 2022. Vol. 122. N6. P. 6634–6718. https://doi.org/10.1021/acs.chemrev.1c00795
  5. Шевченко В. П., Нагаев И. Ю., Шапошников А. И., Шевченко К. В., Белимов А. А., Баташева С. Н., Гоголева Н. Е., Гоголев Ю. В., Мясоедов Н. Ф. // Докл. АН. 2018. Т. 483. № 3. C. 274–278. https://doi.org/10.31857/S086956520003247-4
  6. Smarun A. V., Petkovic M., Shchepinov M. S., Vidovic D. // J. Org. Chem. 2017. Vol. 82. N24. P. 13115–13120. https://doi.org/10.1021/acs.joc.7b02169
  7. Esaki H., Ito N., Sakai Sh., Maegawa T., Monguchi Y., Sajiki H. // Tetrahedron. 2006. Vol. 62. N47. P. 10954–10961. https://doi.org/10.1016/j.tet.2006.08.088
  8. Chiesa M., Giamello E., Murphy D. M., Pacchioni G., Paganini M. C., Soave R., Sojka Z. // J. Phys. Chem. B. 2001. Vol. 105. N2. P. 497–505. https://doi.org/10.1021/jp002794+
  9. Chiesa M., Giamello E., Paganini M. C. // J. Chem. Phys. 2002. Vol. 116. N10. P. 4266–4274. https://doi.org/10.1063/1.1447907
  10. Chiesa M., Paganini M. C., Spoto G., Giamello E., Di Valentin C., Del Vitto A., Pacchioni G. // J. Phys. Chem. B. 2005. Vol. 109. N15. P. 7314–7322. https://doi.org/10.1021/jp044783c
  11. Chiesa M., Paganini M. C., Giamello E., Murphy D. M., Di Valentin C., Pacchioni G. //Acc. Chem. Res. 2006. Vol. 39. N11. P. 861–867. https://doi.org/10.1021/ar068144r
  12. Борисов Ю. А., Золотарев Ю. А. // ЖФХ. 2002. Т. 76. № 4. С. 727–731.
  13. Bhering D. L., Ramirez-Solis A., Mota C. J.A. // J. Phys. Chem. B. 2003. Vol. 107. N18. P. 4342–4347. https://doi.org/10.1021/jp022331z
  14. Kresse G., Furthmuller J. // Comput. Mater. Sci. 1996. Vol. 6. N1. P. 15–50. https://doi.org/10.1016/0927-0256(96)00008-0
  15. Zheng A., Li Sh., Liu Sh.-B., Deng F. // Acc. Chem. Res. 2016. Vol. 49. N4. P. 655–663. https://doi.org/10.1021/acs.accounts.6b00007
  16. Баитов А. А., Сидоров Г. В., Мясоедов Н. Ф. // Радиохимия. 2011. Т. 53. № 3. С. 282–284.

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2. Fig.

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3. Scheme 1. The introduction of deuterium into polyunsaturated fatty acids.

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4. 1. Peptide isotopomers formed during treatment of the Boc-Trp-Pro-Pro-Trp-5% Pd/Al2O3–Al2O3 mixture (1 :5 : 30): (a) D2 (solid-phase method), 170°C; (b) D2O (liquid-phase method), 150°C.

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5. 2. Peptide isotopomers formed during isotopic exchange with D2O after pretreatment of the D2 mixture Boc-Trp-Pro-Pro-Trp-5% Pd/Al2O3–Al2O3 (1 : 5 : 30).

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