Effects of N-terminal modifications on the stability of antimicrobial peptide SAMP-A4 analogues against protease degradation.

Autor: Li R; College of Biological Engineering, Henan University of Technology, Zhengzhou, China., He S; College of Biological Engineering, Henan University of Technology, Zhengzhou, China., Yin K; College of Information Science and Engineering, Henan University of Technology, Zhengzhou, China., Zhang B; College of Biological Engineering, Henan University of Technology, Zhengzhou, China., Yi Y; College of Biological Engineering, Henan University of Technology, Zhengzhou, China., Zhang M; College of Biological Engineering, Henan University of Technology, Zhengzhou, China., Pei N; College of Biological Engineering, Henan University of Technology, Zhengzhou, China., Huang L; College of Biological Engineering, Henan University of Technology, Zhengzhou, China.
Jazyk: angličtina
Zdroj: Journal of peptide science : an official publication of the European Peptide Society [J Pept Sci] 2021 Oct; Vol. 27 (10), pp. e3352. Date of Electronic Publication: 2021 May 24.
DOI: 10.1002/psc.3352
Abstrakt: Infections with multidrug-resistant (MDR) pathogens are increasingly concerning for public health. Synthesized antimicrobial peptide A4 (SAMP-A4), a peptide computationally designed by our research team, is a potential drug candidate. However, the antimicrobial peptide SAMP-A4 is easily degraded in serum. To obtain SAMP-A4 analogues with high biostability, chemical modifications at its N-terminus, including fatty acid conjugation, glycosylation and PEGylation, were carried out. The results showed that the introduction of hydrophobic fatty acids at the N-terminus of SAMP-A4 is better than hydrophilic glycosylation and PEGylation. With increasing fatty acid chain length, the stability of SAMP-A4 analogues in serum and trypsin solutions is significantly improved, and the activities against MDR bacteria and Candida are significantly enhanced. There is no obvious change in haemolysis even when hexanoic acid is coupled with SAMP-A4, so the resulting analogue SAMP-A4-C6, SAMP-A4 conjugated with hexanoic acid, is the most likely of the analogues to become a drug.
(© 2021 European Peptide Society and John Wiley & Sons, Ltd.)
Databáze: MEDLINE
Externí odkaz: