Ghosh Anupam, Mukhopadhyay Titas Kumar, Datta Ayan
School of Chemical Sciences, Indian Association for the Cultivation of Science, Jadavpur - 700032, West Bengal, India.
Nanoscale. 2022 Dec 22;15(1):321-336. doi: 10.1039/d2nr05096j.
Cyclotides are backbone-cyclized peptides of plant origin enriched with disulfide bonds, having exceptional stability towards thermal denaturation and proteolytic degradation. They have a plethora of activities like antibacterial, antifungal, anti-tumor and anti-HIV properties predominantly owing to their selective interaction with certain phospholipids, thereby leading to the disruption of cellular membranes. On the other hand, low-dimensional materials like graphene and hexagonal boron nitride (-BN) are also known to show membrane-proliferating activities through lipid extraction. A plausible and more effective antibacterial, anti-tumor and antifungal agent would be a composite of these 2D materials and cyclotides, provided the structures of the peptides remain unperturbed upon adsorption and interaction. In this study, classical molecular dynamics simulations are performed to understand the nature of adsorption of cyclotides belonging to different families on graphene and -BN and analyze the resulting structural changes. It is revealed that, due to their exceptional structural stability, cyclotides maintain their structural integrity upon adsorption on the 2D materials. In addition, the aggregated states of the cyclotides, which are ubiquitous in plant organs, are also not disrupted upon adsorption. Extensive free energy calculations show that the adsorption strength of the cyclotides is moderate in comparison to those of other similar-sized biomolecules, and the larger the size of the aggregates, the weaker the binding of individual peptides with the 2D materials, thereby leading to their lower release times from the materials. It is predicted that graphene and -BN may safely be used for the preparation of composites with cyclotides, which in turn may be envisaged to be probable candidates for manufacturing next-generation bionano agents for agricultural, antibacterial and therapeutic applications.
环肽是植物来源的具有丰富二硫键的主链环化肽,对热变性和蛋白水解降解具有非凡的稳定性。它们具有多种活性,如抗菌、抗真菌、抗肿瘤和抗HIV特性,主要是由于它们与某些磷脂的选择性相互作用,从而导致细胞膜的破坏。另一方面,像石墨烯和六方氮化硼(-BN)这样的低维材料也已知通过脂质提取表现出膜增殖活性。如果肽的结构在吸附和相互作用时保持不受干扰,那么一种合理且更有效的抗菌、抗肿瘤和抗真菌剂将是这些二维材料与环肽的复合物。在本研究中,进行了经典分子动力学模拟,以了解不同家族的环肽在石墨烯和 -BN上的吸附性质,并分析由此产生的结构变化。结果表明,由于其非凡的结构稳定性,环肽在吸附到二维材料上时保持其结构完整性。此外,在植物器官中普遍存在的环肽聚集态在吸附时也不会被破坏。广泛的自由能计算表明,与其他类似大小的生物分子相比,环肽的吸附强度适中,并且聚集体的尺寸越大,单个肽与二维材料的结合越弱,从而导致它们从材料中的释放时间越短。据预测,石墨烯和 -BN可安全地用于制备与环肽的复合材料,进而可设想它们可能是制造用于农业、抗菌和治疗应用的下一代生物纳米剂的候选材料。