Helbik-Maciejewska Aleksandra, Gitlin-Domagalska Agata, Glavaš Mladena, Ptaszyńska Natalia, Dębowski Dawid, Łęgowska Anna, Rolka Krzysztof
Department of Molecular Biochemistry, Faculty of Chemistry, University of Gdansk, Wita Stwosza 63, 80-308 Gdańsk, Poland.
Department of Organic Chemistry and Biochemistry, Rud̵er Bošković Institute, Bijenička c. 54, 10 000 Zagreb, Croatia.
J Org Chem. 2025 Jun 6;90(22):7182-7190. doi: 10.1021/acs.joc.5c00083. Epub 2025 May 23.
Backbone N-methylation is a pivotal peptide modification that enhances lipophilicity, metabolic stability, and binding affinity or specificity, thereby improving bioactive peptides' bioavailability. Substitution of a backbone amide hydrogen with a methyl group is a three-step procedure which is fully integrated with solid-phase peptide synthesis strategy and usually takes about 4 h. We have revolutionized this process by optimizing the method and slashing the total N-methylation procedure time from 4 h to just 40 min. Moreover, we demonstrate that N-methylation can be equally efficient regardless of the laboratory equipment used, such as a standard laboratory shaker, microwave synthesizer, or common ultrasonic bath. Our study not only results in acceleration of the N-methylation process during solid-phase peptide synthesis but also offers a flexible choice of laboratory equipment, making peptide modifications more efficient and achievable.
主链N-甲基化是一种关键的肽修饰,可增强亲脂性、代谢稳定性以及结合亲和力或特异性,从而提高生物活性肽的生物利用度。用甲基取代主链酰胺氢是一个三步过程,该过程与固相肽合成策略完全整合,通常需要约4小时。我们通过优化方法并将总N-甲基化过程时间从4小时大幅缩短至仅40分钟,彻底改变了这一过程。此外,我们证明,无论使用何种实验室设备,如标准实验室振荡器、微波合成仪或普通超声浴,N-甲基化都能同样高效。我们的研究不仅加快了固相肽合成过程中的N-甲基化进程,还提供了灵活的实验室设备选择,使肽修饰更高效且可实现。