Department of Chemistry, Brandeis University, 415 South Street, Waltham, Massachusetts 02454, USA.
Langmuir. 2012 Sep 18;28(37):13512-7. doi: 10.1021/la302583a. Epub 2012 Sep 4.
Here we report the examination of two convenient strategies, the use of a d-amino acid residue or a glycoside segment, for increasing the proteolytic resistance of supramolecular hydrogelators based on small peptides. Our results show that the introduction of d-amino acid or glycoside to the peptides significantly increases the resistance of the hydrogelators against proteinase K, a powerful endopeptidase. The insertion of d-amino acid in the peptide backbone, however, results relatively low storage moduli of the hydrogels, likely due to the disruption of the superstructures of the molecular assembly. In contrast, the introduction of a glycoside to the C-terminal of peptide enhances the biostability of the hydrogelators without the significant decrease of the storage moduli of the hydrogels. This work suggests that the inclusion of a simple glycogen in hydrogelators is a useful approach to increase their biostability, and the gained understanding from the work may ultimately lead to development of hydrogels of functional peptides for biomedical applications that require long-term biostability.
在这里,我们报告了两种方便的策略的研究,即使用 d-氨基酸残基或糖苷片段来提高基于小肽的超分子水凝胶的抗蛋白酶水解能力。我们的结果表明,在肽中引入 d-氨基酸或糖苷可以显著提高水凝胶对蛋白酶 K(一种强大的内肽酶)的抗性。然而,在肽骨架中插入 d-氨基酸会导致水凝胶的储能模量相对较低,这可能是由于分子组装的超结构被破坏。相比之下,在肽的 C 末端引入糖苷可以增强水凝胶的生物稳定性,而不会显著降低水凝胶的储能模量。这项工作表明,在水凝胶中加入简单的糖原是提高其生物稳定性的一种有效方法,从这项工作中获得的认识最终可能会导致开发用于需要长期生物稳定性的生物医学应用的功能性肽水凝胶。