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ЖУРНАЛЫ // Mendeleev Communications // Архив

Mendeleev Commun., 2025, том 35, выпуск 2, страницы 136–138 (Mi mendc1364)

Communications

Site-specific sortase-catalyzed lipidation of proteins

T. D. Melikhovaa, N. V. Bovina, N. S. Shoshinab, T. V. Bobika, L. A. Gavrilova, M. A. Sablinaa, E. M. Rapoporta, V. N. Stepanenkob, A. B. Tuzikova

a M. M. Shemyakin–Yu. A. Ovchinnikov Institute of Bioorganic Chemistry, Russian Academy of Sciences, 117997 Moscow, Russian Federation
b I. M. Sechenov First Moscow State Medical University, 119991 Moscow, Russian Federation


Аннотация: A methodology for the enzymatic ligation of proteins with a lipid is proposed, a feature of which is the use of a hydrophilized [thanks to a CMG(2) spacer] and therefore highly water-soluble lipid. Its H2N-Gly5 terminus and the recombinant protein amino acid sequence LPETG are substrates of the enzyme sortase A. Two lipid-ligated proteins, red fluorescent mCherry and Protein A, are shown to be inserted into the cell membrane.

Ключевые слова: bioconjugation, lipid tag, sortase А, protein A, mCherry, CMG.

Поступила в редакцию: 10.09.2024
Принята в печать: 28.10.2024

Язык публикации: английский

DOI: 10.71267/mencom.7613



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