Institute of Biomaterial Science and Berlin-Brandenburg Center for Regenerative Therapies (BCRT), Helmholtz-Zentrum Geesthacht, Kantstrasse 55, 14513 Teltow, Germany; Institute of Chemistry, University of Potsdam, 14476 Potsdam-Golm, Germany.
Institute of Biomaterial Science and Berlin-Brandenburg Center for Regenerative Therapies (BCRT), Helmholtz-Zentrum Geesthacht, Kantstrasse 55, 14513 Teltow, Germany.
Acta Biomater. 2016 Jul 1;38:1-10. doi: 10.1016/j.actbio.2016.04.018. Epub 2016 Apr 21.
The extracellular matrix (ECM) is a nano-structured, highly complex hydrogel, in which the macromolecules are organized primarily by non-covalent interactions. Here, in a biomimetic approach, the decorin-derived collagen-binding peptide LSELRLHNN was grafted to hyaluronic acid (HA) in order to enable the formation of a supramolecular hydrogel network together with collagen. The storage modulus of a mixture of collagen and HA was increased by more than one order of magnitude (G'=157Pa) in the presence of the HA-grafted peptide compared to a mixture of collagen and HA (G'=6Pa). The collagen fibril diameter was decreased, as quantified using electron microscopy, in the presence of the HA-grafted peptide. Here, the peptide mimicked the function of decorin by spatially organizing collagen. The advantage of this approach is that the non-covalent crosslinks between collagen molecules and the HA chains created by the peptide form a reversible and dynamic hydrogel, which could be employed for a diverse range of applications in regenerative medicine.
Biopolymers of the extracellular matrix (ECM) like collagen or hyaluronan are attractive starting materials for biomaterials. While in biomaterial science covalent crosslinking is often employed, in the native ECM, stabilization and macromolecular organization is primarily based on non-covalent interactions, which allows dynamic changes of the materials. Here, we show that collagen-binding peptides, derived from the small proteoglycan decorin, grafted to hyaluronic acid enable supramolecular stabilization of collagen hydrogels. These hydrogels have storage moduli more than one order of magnitude higher than mixtures of collagen and hyaluronic acid. Furthermore, the peptide supported the structural organization of collagen. Such hydrogels could be employed for a diverse range of applications in regenerative medicine. Furthermore, the rational design helps in the understanding ECM structuring.
细胞外基质 (ECM) 是一种纳米结构的高度复杂的水凝胶,其中大分子主要通过非共价相互作用进行组织。在这里,采用仿生方法,将源自 decorin 的胶原结合肽 LSELRLHNN 接枝到透明质酸 (HA) 上,以便与胶原一起形成超分子水凝胶网络。与胶原和 HA 的混合物相比,在存在接枝有 HA 的肽的情况下,胶原和 HA 的混合物的储能模量增加了一个数量级以上 (G'=157Pa)。如电子显微镜定量所示,在存在接枝有 HA 的肽的情况下,胶原纤维直径减小。在这里,该肽通过空间组织胶原模仿了 decorin 的功能。该方法的优点是,由肽形成的胶原分子和 HA 链之间的非共价交联形成了一种可逆和动态的水凝胶,可用于再生医学的各种应用。
细胞外基质 (ECM) 的生物聚合物,如胶原或透明质酸,是生物材料的有吸引力的起始材料。虽然在生物材料科学中经常使用共价交联,但在天然 ECM 中,稳定和大分子组织主要基于非共价相互作用,这允许材料的动态变化。在这里,我们表明,从小蛋白聚糖 decorin 衍生的胶原结合肽接枝到透明质酸上,能够使胶原水凝胶实现超分子稳定化。这些水凝胶的储能模量比胶原和透明质酸混合物高一个数量级以上。此外,该肽支持胶原的结构组织。这种水凝胶可用于再生医学的各种应用。此外,合理的设计有助于理解 ECM 的结构。