Faculty of Chemistry, University of Gdańsk, Gdańsk, Poland.
Methods Mol Biol. 2024;2714:143-153. doi: 10.1007/978-1-0716-3441-7_8.
Glycosaminoglycans (GAGs) are a class of long linear anionic periodic polysaccharides. Their biological activities are very broad including tissue remodeling, regulation of cell proliferation, cell migration, cell differentiation, participation in bacterial/viral infections, and immune response. They can interact with many important biomolecular partners in the extracellular matrix of the cell including small drug molecules. Recently, several GAG-bioactive small molecule complexes have been experimentally and theoretically studied. Some of these compounds in complexes with GAGs may potentially interfere with protein-GAG or peptide-GAG multimolecular systems affecting the processes of cellular differentiation or have anti-inflammatory, antiviral as well as antithrombotic effects. Although many studies have been conducted on GAG-drug complexes, the molecular mechanisms of the formation of such complexes are still poorly understood. At the same time, the complexity of their physicochemical properties renders the use of both experimental and computational methods to study these molecular systems challenging. Here, we present the molecular dynamics-based protocols successfully employed to in silico analyze GAG-small molecule interactions.
糖胺聚糖(GAGs)是一类长线性阴离子周期性多糖。它们的生物活性非常广泛,包括组织重塑、调节细胞增殖、细胞迁移、细胞分化、参与细菌/病毒感染和免疫反应。它们可以与细胞外基质中的许多重要生物分子伴侣相互作用,包括小分子药物。最近,已经对几种 GAG-生物活性小分子复合物进行了实验和理论研究。这些与 GAG 结合的化合物中的一些可能潜在地干扰蛋白-GAG 或肽-GAG 多分子系统,影响细胞分化过程,具有抗炎、抗病毒和抗血栓形成作用。尽管已经对 GAG-药物复合物进行了许多研究,但形成这些复合物的分子机制仍知之甚少。同时,它们物理化学性质的复杂性使得使用实验和计算方法来研究这些分子系统具有挑战性。在这里,我们展示了基于分子动力学的成功协议,用于计算机分析 GAG-小分子相互作用。