Key Laboratory for Molecular Enzymology and Engineering of the Ministry of Education, Jilin University, Changchun 130012, China.
School of Life Sciences, Jilin University, Changchun 130012, China.
Int J Mol Sci. 2017 Dec 27;19(1):67. doi: 10.3390/ijms19010067.
V13K, a 26-residue peptide, has been shown to have strong antimicrobial activity, negligible hemolytic activity, and significant anticancer activity. In the present work, V13K was used as the framework to investigate the influence of helicity, as influenced by d-amino acid substitutions in the center of the peptide polar and non-polar faces of the amphipathic helix, on biological activity. The antibacterial and anticancer activities of the peptides were investigated. Atomic force microscopy and other biophysical methods were used to investigate the effect of peptide helicity on biological activity. The results showed the importance of suitable and rational modification of membrane-active peptides, based on helicity, in optimizing potential biological activity.
V13K 是一种 26 个氨基酸组成的肽,具有很强的抗菌活性、极小的溶血活性和显著的抗癌活性。在本工作中,V13K 被用作框架,研究了肽的亲水头和疏水尾的中心的 d-氨基酸取代对螺旋的影响,从而影响其螺旋性,进而对生物活性的影响。研究了这些肽的抗菌和抗癌活性。原子力显微镜和其他生物物理方法用于研究肽的螺旋性对生物活性的影响。结果表明,基于螺旋性,适当合理地修饰膜活性肽对于优化潜在的生物活性非常重要。