Synthesis of steroid tracers with a oxyme ligation method and use thereof in fluorescent polarisation immunoassay
- Авторлар: Prokhorenko I.A.1, Glushchenko D.A.1, Gulyak E.L.1, Mikhura I.V.1, Korshun V.A.1, Mukhametova L.I.2, Eremin S.А.2
-
Мекемелер:
- Shemyakin–Ovchinnikov Institute of Bioorganic Chemistry RAS
- Lomonosov Moscow State University
- Шығарылым: Том 50, № 1 (2024)
- Беттер: 51-64
- Бөлім: Articles
- URL: https://ter-arkhiv.ru/0132-3423/article/view/671002
- DOI: https://doi.org/10.31857/S0132342324010055
- EDN: https://elibrary.ru/OWPZNS
- ID: 671002
Дәйексөз келтіру
Аннотация
A method for the synthesis of ketosteroid oxime conjugates with a fluorescein (6-FAM) derivative connected via a short bifunctional aminooxypropyl linker is proposed. The conjugates were used as tracers for fluorescence polarization immunoassay (FPIA) with monoclonal antibodies. Stereoisomers by the oxime group were separated by preparative RP TLC and HPLC and tested in the FPIA method. Binding parameters of of tracers with monoclonal antibodies (mAbs) to progesterone were studied. Tracers showed high efficiency in the analysis of steroid hormones, the detection limit of progesterone being lower than that for a previously described analog. The Z-isomer was found to be more sensitive in the FPIA analysis compared to the E-isomer.
Негізгі сөздер
Толық мәтін

Авторлар туралы
I. Prokhorenko
Shemyakin–Ovchinnikov Institute of Bioorganic Chemistry RAS
Хат алмасуға жауапты Автор.
Email: prig67@mail.ru
Ресей, ul. Miklukho-Maklaya 16/10, Moscow, 117997
D. Glushchenko
Shemyakin–Ovchinnikov Institute of Bioorganic Chemistry RAS
Email: prig67@mail.ru
Ресей, ul. Miklukho-Maklaya 16/10, Moscow, 117997
E. Gulyak
Shemyakin–Ovchinnikov Institute of Bioorganic Chemistry RAS
Email: prig67@mail.ru
Ресей, ul. Miklukho-Maklaya 16/10, Moscow, 117997
I. Mikhura
Shemyakin–Ovchinnikov Institute of Bioorganic Chemistry RAS
Email: prig67@mail.ru
Ресей, ul. Miklukho-Maklaya 16/10, Moscow, 117997
V. Korshun
Shemyakin–Ovchinnikov Institute of Bioorganic Chemistry RAS
Email: prig67@mail.ru
Ресей, ul. Miklukho-Maklaya 16/10, Moscow, 117997
L. Mukhametova
Lomonosov Moscow State University
Email: prig67@mail.ru
Department of Chemistry
Ресей, Leninskiye Gory 1/3, Moscow, 119991S. Eremin
Lomonosov Moscow State University
Email: prig67@mail.ru
Department of Chemistry
Ресей, Leninskiye Gory 1/3, Moscow, 119991Әдебиет тізімі
- Zamri M.F.M.A., Bahru R., Pramanik S.K., Fattah I.M.R. // J. Water Proc. Engin. 2021. V. 41. 102017. https://doi.org/10.1016/j.jwpe.2021.102017
- Miller W.L., Auchus R.J. // Endocr. Rev. 2011. V. 32. P. 81. https://doi.org/10.1210/ER.2010-0013
- Куджаев А.М., Андрианова А.Г., Гущина А.Е., Смирнов И.В., Ротанова Т.В. // Биоорг. химия. Т. 48. С. 381–414. [Kudzhaev A.M., Andrianova A.G., Gustchina A.E., Smirnov I.V., Rotanova T.V. // Russ. J. Bioorg. Chem. 2022. V. 48. P. 678–709.] https://doi.org/10.1134/S1068162022040136
- Gore A.C. // JAMA Int. Med. 2016. V. 176. P. 1705–1706. https://doi.org/10.1001/jamainternmed.2016.5766
- Abraham G.E. // J. Steroid Biochem. 1975. V. 6. P. 261–270. https://doi.org/10.1016/0022-4731(75)90141-7
- Relave F., Lefebvre R.C., Beaudoin S., Price C. // Can. Vet. J. 2007. V. 48. P. 823–826.
- Stanczyk F.Z., Lee J.S., Santen R.J. // Cancer Epidemiol. Biomarkers Prev. 2007. V. 16. P. 1713–1719. https://doi.org/10.1158/1055-9965.EPI-06-0765
- Tate J., Ward G. // Clin. Biochem. Rev. 2004. V. 25. P. 105–120.
- Hall M.D., Yasgar A., Peryea T., Braisted J.C., Jadhav A., Simeonov A., Coussens N.P. // Methods Appl. Fluoresc. 2016. V. 4. P. 022001. https://doi.org/10.1088/2050-6120/4/2/022001
- Smith D.S., Eremin S.A. // Anal. Bioanal. Chem. 2008. V. 391. P. 1499–1507. https://doi.org/10.1007/s00216-008-1897-z
- Choi M.J., Choi J., Yoon D.Y., Park J., Eremin S.A. // Biol. Pharm. Bull. 1997. V. 20. P. 309–314. https://doi.org/10.1248/bpb.20.309
- Колосова A.Ю., Еремин С.А., Гаврилова Е.М., Егоров А.М. // Проблемы эндокринологии. 1994. Т. 40. С. 48–51. https://doi.org/10.14341/probl12147
- Hong J.Y., Choi M.J. // Biol. Pharm. Bull. 2002. V. 25. P. 1258–1262. https://doi.org/10.1248/bpb.25.1258
- Quémener D., Davis T.P., Barner-Kowollik C., Stenzel M.H. // Chem. Commun. 2006. V. 48. P. 5051–5053. https://doi.org/10.1039/B611224B
- Clède S., Lambert F., Sandt C., Kascakova S., Unger M., Harté E., Plamont M.-A., Saint-Forth R., Deniset- Besseau A., Guerouiab Z., Hirschmugl C., Lecomte S., Dazzi A., Vessières A., Policar C. // Analyst. 2013. V. 138. P. 5627–5638. https://doi.org/10.1039/C3AN00807J
- Robinson S.W., Beer P.D. // Org. Biomol. Chem. 2017. V. 15. P. 153–159. https://doi.org/10.1039/ c6ob02339h
- Khomutov A.R., Vepsalainen J.J., Shvetsov A.S., Hyvönen T., Keinänen T.A., Pustobaev V.N., Eloranta T.O., Khomutov R.M. // Tetrahedron. 1996. V. 52. P. 13751–13766. https://doi.org/10.1016/0040-4020(96)00836-8
- Sapozhnikova A., Misyurin V.A., Ryazantsev D.Y., Kokin E.A., Finashutina Yu.P., Alexeeva A.V., Ivanov I.A., Kocharovskaya M.V., Tikhonova N.A., Popova G.P., Alferova V.A., Ustinov A.V., Korshun V.A., Brylev V.A. // Int. J. Mol. Sci. 2022. V. 22. P. 12845. https://doi.org/10.3390/ijms222312845
- Kolmer D.K., Cool E.T. // Chem. Rev. 2017. V. 117. P. 10358–10376. https://doi.org/10.1021/acs.chemrev.7b00090
- Adamczyk M., Chen Y.-Y., Grote J., Mattingly P.G. // Steroids. 1999. V. 64. P. 283–290. https://doi.org/10.1016/S0039-128X(99)00004-5
- Мухаметова Л.И., Крылов В.Б., Соловьев A.C., Яшунский Д.В., Матвеев A.Л., Тикунова Н.В., Еремин С.А., Нифантьев Н.Э. // Известия Акад. наук. Сер. хим. 2021. №. 5. С. 975–981.
- Zhao Q., Bai Y., Wang H. // Talanta. 2020. V. 217. P. 121018. https://doi.org/10.1016/j.talanta.2020.121018
Қосымша файлдар
