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设计基于卡丹基序肽和肝素的多组分高级生物活性水凝胶支架以控制细胞行为。

Designing Cardin-Motif Peptide and Heparin-Based Multicomponent Advanced Bioactive Hydrogel Scaffolds to Control Cellular Behavior.

作者信息

Sen Sourav, Sharma Pooja, Pal Vijay Kumar, Roy Sangita

机构信息

Institute of Nano Science and Technology (INST), Sector 81, Knowledge City, 140306 Mohali, Punjab India.

出版信息

Biomacromolecules. 2023 Nov 13;24(11):4923-4938. doi: 10.1021/acs.biomac.3c00621. Epub 2023 Nov 1.

Abstract

Recently, peptide and sugar-based multicomponent systems have gained much interest in attaining the sophisticated structure and biofunctional complexity of the extracellular matrix (ECM). To this direction, we have designed for the first time a biologically relevant minimalist Cardin-motif peptide capable of binding ECM-derived glycosaminoglycans. Herein, we explored Cardin-motif peptide and heparin-based biomolecular matrix by employing simple noncovalent interactions at the molecular level. Interestingly, this peptide was inadequate to induce hydrogelation at ambient pH due to the presence of basic amino acids. However, addition of heparin successfully triggered its gelation at physiological pH following favorable electrostatic interactions with heparin. Importantly, the newly developed scaffolds displayed tunable nanofibrous morphology and superior mechanical properties as controlled simply by the differential mixing ratio of both biomolecular entities. Additionally, these composite scaffolds could closely mimic the complexity of ECM as they demonstrated superior biocompatibility and enhanced growth and proliferation of neural cells as compared to the peptide scaffold.

摘要

最近,基于肽和糖的多组分系统在实现细胞外基质(ECM)复杂结构和生物功能复杂性方面引起了广泛关注。在此方向上,我们首次设计了一种与生物学相关的简约型卡丹基序肽,它能够结合ECM衍生的糖胺聚糖。在此,我们通过在分子水平上采用简单的非共价相互作用,探索了卡丹基序肽和基于肝素的生物分子基质。有趣的是,由于存在碱性氨基酸,该肽在环境pH下不足以诱导水凝胶化。然而,加入肝素后,与肝素发生有利的静电相互作用,成功地在生理pH下触发了其凝胶化。重要的是,新开发的支架呈现出可调节的纳米纤维形态和优异的机械性能,这只需通过两种生物分子实体的不同混合比例就能简单控制。此外,这些复合支架能够紧密模拟ECM的复杂性,因为与肽支架相比,它们表现出卓越的生物相容性,并能促进神经细胞的生长和增殖。

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