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Электронный каталог: Luginina, A. - Functional GPCR Expression in Eukaryotic LEXSY System
Luginina, A. - Functional GPCR Expression in Eukaryotic LEXSY System
Статья
Автор: Luginina, A.
Journal of Molecular Biology [Electronic resource]: Functional GPCR Expression in Eukaryotic LEXSY System
б.г.
ISBN отсутствует
Автор: Luginina, A.
Journal of Molecular Biology [Electronic resource]: Functional GPCR Expression in Eukaryotic LEXSY System
б.г.
ISBN отсутствует
Статья
Luginina, A.
Functional GPCR Expression in Eukaryotic LEXSY System / A.Luginina, V.Borshchevskiy, [et al.] // Journal of Molecular Biology [Electronic resource]. – 2023. – Vol.435, No.23. – P.168310. – URL: https://doi.org/10.1016/j.jmb.2023.168310. – Bibliogr.:64.
G protein-coupled receptors (GPCRs) form the largest superfamily of membrane proteins in the human genome, and represent one of the most important classes of drug targets. Their structural studies facilitate rational drug discovery. However, atomic structures of only about 20% of human GPCRs have been solved to date. Recombinant production of GPCRs for structural studies at a large scale is challenging due to their low expression levels and stability. Therefore, in this study, we explored the efficacy of the eukaryotic system LEXSY (Leishmania tarentolae) for GPCR production. We selected the human A&sub(2A) adenosine receptor (A&sub(2A)AR), as a model protein, expressed it in LEXSY, purified it, and compared with the same receptor produced in insect cells, which is the most popular expression system for structural studies of GPCRs. The A&sub(2A)AR purified from both expression systems showed similar purity, stability, ligand-induced conformational changes and structural dynamics, with a remarkably higher protein yield in the case of LEXSY expression. Overall, our results suggest that LEXSY is a promising platform for large-scale production of GPCRs for structural studies.
Спец.(статьи,препринты) = 28.0 - Биология$
Спец.(статьи,препринты) = С 44 б - Разделение химических элементов экстракционными и ионообменными методами
ОИЯИ = ОИЯИ (JINR)2023
Бюллетени = 9/024
Luginina, A.
Functional GPCR Expression in Eukaryotic LEXSY System / A.Luginina, V.Borshchevskiy, [et al.] // Journal of Molecular Biology [Electronic resource]. – 2023. – Vol.435, No.23. – P.168310. – URL: https://doi.org/10.1016/j.jmb.2023.168310. – Bibliogr.:64.
G protein-coupled receptors (GPCRs) form the largest superfamily of membrane proteins in the human genome, and represent one of the most important classes of drug targets. Their structural studies facilitate rational drug discovery. However, atomic structures of only about 20% of human GPCRs have been solved to date. Recombinant production of GPCRs for structural studies at a large scale is challenging due to their low expression levels and stability. Therefore, in this study, we explored the efficacy of the eukaryotic system LEXSY (Leishmania tarentolae) for GPCR production. We selected the human A&sub(2A) adenosine receptor (A&sub(2A)AR), as a model protein, expressed it in LEXSY, purified it, and compared with the same receptor produced in insect cells, which is the most popular expression system for structural studies of GPCRs. The A&sub(2A)AR purified from both expression systems showed similar purity, stability, ligand-induced conformational changes and structural dynamics, with a remarkably higher protein yield in the case of LEXSY expression. Overall, our results suggest that LEXSY is a promising platform for large-scale production of GPCRs for structural studies.
Спец.(статьи,препринты) = 28.0 - Биология$
Спец.(статьи,препринты) = С 44 б - Разделение химических элементов экстракционными и ионообменными методами
ОИЯИ = ОИЯИ (JINR)2023
Бюллетени = 9/024