Skoulas Dimitrios, Fallon Muireann, Genoud Katelyn J, O'Brien Fergal J, Hughes Deirdre Fitzgerald, Heise Andreas
Department of Chemistry, RCSI University of Medicine and Health Sciences, 123 St. Stephen's Green, D02 YN77 Dublin, Ireland.
Department of Clinical Microbiology, Royal College of Surgeons in Ireland, RCSI Education and Research, Beaumont Hospital, Beaumont, D09 V2N0 Dublin, Ireland.
Gels. 2024 Oct 11;10(10):652. doi: 10.3390/gels10100652.
Hydrogels with low toxicity, antimicrobial potency and shear-thinning behavior are promising materials to combat the modern challenges of increased infections. Here, we report on 8-arm star block copolypeptides based on poly(L-lysine), poly(L-tyrosine) and poly(S-benzyl-L-cysteine) blocks. Three star block copolypeptides were synthesized with poly(S-benzyl-L-cysteine) always forming the outer block. The inner block comprised either two individual blocks of poly(L-lysine) and poly(L-tyrosine) or a statistical block copolypeptide from both amino acids. The star block copolypeptides were synthesized by the Ring Opening Polymerization (ROP) of the protected amino acid N-carboxyanhydrides (NCAs), keeping the overall ratio of monomers constant. All star block copolypeptides formed hydrogels and Scanning Electron Microscopy (SEM) confirmed a porous morphology. The investigation of their viscoelastic characteristics, water uptake and syringe extrudability revealed superior properties of the star polypeptide with a statistical inner block of L-lysine and L-tyrosine. Further testing of this sample confirmed no cytotoxicity and demonstrated antimicrobial activity of 1.5-log and 2.6-log reduction in colony-forming units, CFU/mL, against colony-forming reference laboratory strains of Gram-negative and Gram-positive , respectively. The results underline the importance of controlling structural arrangements in polypeptides to optimize their physical and biological properties.
具有低毒性、抗菌效力和剪切变稀行为的水凝胶是应对感染增加这一现代挑战的有前景的材料。在此,我们报道基于聚(L-赖氨酸)、聚(L-酪氨酸)和聚(S-苄基-L-半胱氨酸)嵌段的8臂星形嵌段共多肽。合成了三种星形嵌段共多肽,其中聚(S-苄基-L-半胱氨酸)总是形成外层嵌段。内层嵌段由聚(L-赖氨酸)和聚(L-酪氨酸)的两个单独嵌段或由这两种氨基酸组成的统计嵌段共多肽组成。通过受保护氨基酸N-羧基环酸酐(NCA)的开环聚合(ROP)合成星形嵌段共多肽,保持单体的总比例恒定。所有星形嵌段共多肽都形成了水凝胶,扫描电子显微镜(SEM)证实了多孔形态。对其粘弹性特征、吸水性和注射器挤出性的研究表明,具有L-赖氨酸和L-酪氨酸统计内层嵌段的星形多肽具有优异的性能。对该样品的进一步测试证实无细胞毒性,并分别对革兰氏阴性和革兰氏阳性的菌落形成参考实验室菌株显示出1.5对数和2.6对数的菌落形成单位(CFU/mL)减少的抗菌活性。结果强调了控制多肽结构排列以优化其物理和生物学性质的重要性。