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Mendeleev Communications, 2025, Volume 35, Issue 2, Pages 136–138
DOI: https://doi.org/10.71267/mencom.7613
(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
References:
Abstract: 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.
Keywords: bioconjugation, lipid tag, sortase А, protein A, mCherry, CMG.
Received: 10.09.2024
Accepted: 28.10.2024
Document Type: Article
Language: English
Supplementary materials:
Supplementary_data_1.pdf (793.6 Kb)


Citation: T. D. Melikhova, N. V. Bovin, N. S. Shoshina, T. V. Bobik, L. A. Gavrilov, M. A. Sablina, E. M. Rapoport, V. N. Stepanenko, A. B. Tuzikov, “Site-specific sortase-catalyzed lipidation of proteins”, Mendeleev Commun., 35:2 (2025), 136–138
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