Bioluminescent monitoring enables observation of intracellular events in real time without cell and tissue destruction
- Autores: Markova S.V.1,2,3, Malikova N.P.1,2, Vysotski E.S.1,2, Frank L.A.1,2,3, Gitelson I.I.1,2,3
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Afiliações:
- Institute of Biophysics, Federal Research Center Krasnoyarsk Scientific Center, Siberian Branch
- Blokhin Russian Cancer Research Center
- Siberian Federal University
- Edição: Volume 62, Nº 3 (2017)
- Páginas: 503-507
- Seção: Biophysics of Complex Systems
- URL: https://ogarev-online.ru/0006-3509/article/view/152328
- DOI: https://doi.org/10.1134/S0006350917030101
- ID: 152328
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Resumo
Secreted reporter proteins provide monitoring of intracellular events in real time without cell destruction. To create human melanoma cell lines that enables noninvasive bioluminescent monitoring of metabolic activity, a comparison of the efficiency of isoforms and mutant variants of luciferase from the Metridia longa as secreted reporter proteins in the cells of human melanoma lines Mel IL was conducted. The MLM3 deletion mutant had the highest activity in the medium of two studied isoforms and two deletion mutants of secreted M. longa luciferase during the Mel IL melanoma cell transfection. It was established that optimization of the gene structure of the selected MLM3 variant for expression in human cells increases the level of bioluminescent activity in the Mel IL cells by almost an order of magnitude. A stable Mel IL melanoma cell line with constitutive expression of the humanized hMLM3 reporter gene was obtained and characterized. The linear range of identification of living cells by the hMLM3 reporter activity was more than three orders of magnitude with a sensitivity of detection of 10 cells.
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Sobre autores
S. Markova
Institute of Biophysics, Federal Research Center Krasnoyarsk Scientific Center, Siberian Branch; Blokhin Russian Cancer Research Center; Siberian Federal University
Autor responsável pela correspondência
Email: smarkova@mail.ru
Rússia, Akademgorodok 50/50, Krasnoyarsk, 660036; Kashirskoe shosse 24, Moscow, 115478; Svobodny pr. 79, Krasnoyarsk, 660041
N. Malikova
Institute of Biophysics, Federal Research Center Krasnoyarsk Scientific Center, Siberian Branch; Blokhin Russian Cancer Research Center
Email: smarkova@mail.ru
Rússia, Akademgorodok 50/50, Krasnoyarsk, 660036; Kashirskoe shosse 24, Moscow, 115478
E. Vysotski
Institute of Biophysics, Federal Research Center Krasnoyarsk Scientific Center, Siberian Branch; Blokhin Russian Cancer Research Center
Email: smarkova@mail.ru
Rússia, Akademgorodok 50/50, Krasnoyarsk, 660036; Kashirskoe shosse 24, Moscow, 115478
L. Frank
Institute of Biophysics, Federal Research Center Krasnoyarsk Scientific Center, Siberian Branch; Blokhin Russian Cancer Research Center; Siberian Federal University
Email: smarkova@mail.ru
Rússia, Akademgorodok 50/50, Krasnoyarsk, 660036; Kashirskoe shosse 24, Moscow, 115478; Svobodny pr. 79, Krasnoyarsk, 660041
I. Gitelson
Institute of Biophysics, Federal Research Center Krasnoyarsk Scientific Center, Siberian Branch; Blokhin Russian Cancer Research Center; Siberian Federal University
Email: smarkova@mail.ru
Rússia, Akademgorodok 50/50, Krasnoyarsk, 660036; Kashirskoe shosse 24, Moscow, 115478; Svobodny pr. 79, Krasnoyarsk, 660041
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