Synthesis of the ensembles from succinylated interleukin-2 derivatives and their biological activity in vitro

Авторы

  • Artur Martynov ГУ «Институт микробиологии и иммунологии им. И. И. Мечникова Национальной академии медицинских наук Украины» ул. Пушкинская, 14, г. Харьков, Украина, 61057, Ukraine
  • Boris Farber Noigel LLC. Noigel, LLC., Inc. 1781 East 17th Street Suite #D6, Brooklyn, NY 11229 USA, United States
  • Sophia Farber Noigel LLC. Noigel, LLC., Inc. 1781 East 17th Street Suite #D6, Brooklyn, NY 11229 USA, United States
  • Tatiana Kabluchko ГУ «Институт микробиологии и иммунологии им. И. И. Мечникова Национальной академии медицинских наук Украины» ул. Пушкинская, 14, г. Харьков, 61057, Украина, Ukraine

DOI:

https://doi.org/10.15587/2313-8416.2015.53985

Ключевые слова:

Agilent-2100, bioactivity, succinylated interleukin-2, high-performance liquid chromatography, recombinant interleukin-2

Аннотация

Purpose: The biological activity (direct anticancer action in vitro) of combinatorial IL-2 succinylated derivatives was examined. Acylation of IL-2 was performed using succinic anhydride with various levels of acylation, with the formation of a complex assembly of many derivatives (self-assembled quasi-living structure).

Methods: In the study, we used recombinant interleukin-2 (IL-2) (Ronkoleukin, Russia) in oxidizing form and other reagents from Sigma-Aldrich and Fluka (USA). For acylation, recombinant IL-2 in the form of a matrix fluid with a protein concentration of 0.6 mg/ml was used. The IL-2 matrix solution was brought to a pH of 8.0 through the addition of a 0.01% solution of sodium hydroxide. The synthesized ensemble of succinyl-IL-2 was analyzed using the capillary gel electrophoresis method in an Agilent-2100 bioanalyzer. The molecular masses of the synthesized ensemble were established in comparison to standard samples of low-molecular proteins with known molecular masses that were part of the bioanalyzer’s collection. The additional negative charge of the modified IL-2 was determined by a FPLC (Fast Protein Liquid Chromatography) system from Pharmacia (Woerden, Netherlands). CTLL-2, a murine IL-2-dependent cell line, was obtained fromBiokontrol (Kiev, Ukraine). These respondingcells were used in proliferative assays comparing the activityof the IL-2 and succinylated IL-2 derivatives to the WHO InternationalStandard. For statistical data analysis, the one-way ANOVA was used.

Results: After treatment with Suc-IL-2, BTL were studied in vitro on the CTLL-2 cell line, dose-dependently, in a BTL induction reaction. The highest level of biological activity in acylated IL-2 was observed in Suc-IL-2 with four modified lysine residues. In conclusion, succinylated IL-2 with four substituted lysines may be useful as a prospective anticancer agent.

Conclusions: Ten-fold increase in the biological activity of IL-2 was observed after partial succinylation. This phenomenon can be used in the further IL-2 drugs biotechnological development for increasing the concentration of the main active substance in medicinal form

Биографии авторов

Artur Martynov, ГУ «Институт микробиологии и иммунологии им. И. И. Мечникова Национальной академии медицинских наук Украины» ул. Пушкинская, 14, г. Харьков, Украина, 61057

Доктор фармацевтических наук, профессор

Заведующий лаборатории и клинического отдела молекулярной иммунофармакологии (ЛКОМИ)

Boris Farber, Noigel LLC. Noigel, LLC., Inc. 1781 East 17th Street Suite #D6, Brooklyn, NY 11229 USA

Доктор технических наук, профессор

Президент Noigel LLC.

Sophia Farber, Noigel LLC. Noigel, LLC., Inc. 1781 East 17th Street Suite #D6, Brooklyn, NY 11229 USA

Старший исследователь

Tatiana Kabluchko, ГУ «Институт микробиологии и иммунологии им. И. И. Мечникова Национальной академии медицинских наук Украины» ул. Пушкинская, 14, г. Харьков, 61057, Украина

Старший лаборант

Лаборатория и клинический отдел молекулярной иммунофармакологии (ЛКОМИ)

Библиографические ссылки

Adibzadeh, M., Weder, H. G., Rehbein, A., Schwuléra, U., Obermeier, J., Pawelec, G. (1992). Activity of liposomal interleukin-2 in vitro. Mol. Biother. 4 (1), 24–28.

Okuno, K., Nakamura, K., Tanaka, A., Yachi, K., Yasutomi, M. (1998). Hepatic immunopotentiation by galactose-entrapped liposomal IL-2 compound in the treatment of liver metastases. Surg Today, 28 (1), 64–69. doi: 10.1007/bf02483610

Apisarnthanarax, N., Talpur, R., Duvic, M. (2002). Treatment of Cutaneous T Cell Lymphoma. American Journal of Clinical Dermatology, 3 (3), 193–215. doi: 10.2165/00128071-200203030-00006

Martynov, A. V., Smelyanskaya, M. V. (2005). Antiproliferative Properties of Chemically Modified Recombinant IFN-α2b. Journal of Interferon & Cytokine Research, 25 (7), 414–417. doi: 10.1089/jir.2005.25.414

Koppenhagen, F. J., Storm, G., Underberg, W. J. M. (1998). Development of a routine analysis method for liposome encapsulated recombinant interleukin-2. Journal of Chromatography B: Biomedical Sciences and Applications, 716 (1-2), 285–291. doi: 10.1016/s0378-4347(98)00271-0

Hank, J. A., Surfus, J., Gan, J., Albertini, M., Lindstrom, M., Schiller, J. H., Hotton, K. M., Khorsand, M., Sondel, P. M. (1999). Distinct Clinical and Laboratory Activity of Two Recombinant Interleukin-2 Preparations. Clin. Cancer Res., 5 (2), 281–292.

Arkin, M. R., Randal, M., DeLano, W. L., Hyde, J., Luong, T. N., Oslob, J. D. et. al (2003). Binding of small molecules to an adaptive protein-protein interface. Proceedings of the National Academy of Sciences, 100 (4), 1603–1608. doi: 10.1073/pnas.252756299

Rosenberg, S. A. (1988). New Approaches to the Immunotherapy of Cancer Using Interleukin-2. Annals of Internal Medicine, 108 (6), 853. doi: 10.7326/0003-4819-108-6-853

Kohler, P. C., Hank, J. A., Moore, K. H., Storer, B., Bechhofer, R., Sondel, P. M. (1987). Phase I clinical evaluation of recombinant interleukin-2. Prog. Clin. Biol. Res., 244, 161–172.

Lotze, M. T., Matory, Y. L., Rayner, A. A., Ettinghausen, S. E., Vetto, J. T., Seipp, C. A., Rosenberg, S. A. (1986). Clinical effects and toxicity of interleukin-2 in patients with cancer. Cancer, 58 (12), 2764–2772. doi: 10.1002/1097-0142(19861215)58:12<2764::aid-cncr2820581235>3.0.co;2-z

Gearing, A. J. H., Thorpe, R. (1988). The international standard for human interleukin-2. Journal of Immunological Methods, 114 (1-2), 3–9. doi: 10.1016/0022-1759(88)90145-7

Salunkhe, S., Soorapaneni, S., Prasad, K. S., Raiker, V. A., Padmanabhan, S. (2010). Strategies to maximize expression of rightly processed human interferon α2b in Pichia pastoris. Protein Expression and Purification, 71 (2), 139–146. doi: 10.1016/j.pep.2010.02.007

Cohen, J. (1992). A power primer. Psychological Bulletin, 11 2(1), 155–159. doi: 10.1037/0033-2909.112.1.155

Arkin, M. R., Randal, M., DeLano, W. L., Hyde, J., Luong, T. N., Oslob, J. D. et. al (2003). Binding of small molecules to an adaptive protein-protein interface. Proceedings of the National Academy of Sciences, 100 (4), 1603–1608. doi: 10.1073/pnas.252756299

Загрузки

Опубликован

2015-11-29

Выпуск

Раздел

Фармацевтические науки