2012
DOI: 10.1021/la302583a
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Introducing d-Amino Acid or Simple Glycoside into Small Peptides to Enable Supramolecular Hydrogelators to Resist Proteolysis

Abstract: 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 … Show more

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Cited by 86 publications
(70 citation statements)
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“…Unlike Aβ oligomers that resist degradation and accumulate to induce chronic cytotoxicity, the degradation of 1 and other molecular aggregates are rather fast and even tunable. [21] The ability to control the spatiotemporal profiles of the molecular nanofibrils based on the self-assembly of small peptides not only offers a new dimension to control the cytotoxicity of aggregation, but also promises reduced chronic side effect. Moreover, although it remains challenge to provide a simple notion for explaining the lowered Alzheimer’s disease rate in cancer patients, this study on the nanofibrils of 1 offers valuable insights for understanding the lowered cancer rate in Alzheimer’s disease patients.…”
mentioning
confidence: 99%
“…Unlike Aβ oligomers that resist degradation and accumulate to induce chronic cytotoxicity, the degradation of 1 and other molecular aggregates are rather fast and even tunable. [21] The ability to control the spatiotemporal profiles of the molecular nanofibrils based on the self-assembly of small peptides not only offers a new dimension to control the cytotoxicity of aggregation, but also promises reduced chronic side effect. Moreover, although it remains challenge to provide a simple notion for explaining the lowered Alzheimer’s disease rate in cancer patients, this study on the nanofibrils of 1 offers valuable insights for understanding the lowered cancer rate in Alzheimer’s disease patients.…”
mentioning
confidence: 99%
“…Introduction of one Dphenylalanine residue in different positions of naphthalenebased dipeptide gelators was shown to hamper hydrogela-tion. The authors ascribed this fact to reduced intermolecular interactions, and thus reduced formation of superstructures, possibly due to an altered peptide configuration [19]. In another report, introduction of D-amino acids in different positions along a self-assembling peptide sequence led to disruption of the beta-sheet secondary conformation (Fig.…”
Section: Beta-sheetsmentioning
confidence: 98%
“…Alternatively, chymotrypsin, collagenase, cathepsin B, or matrix metalloproteinases (MMP) are useful enzyme models [18]. Overall, increased enzymatic stability towards the action of peptidases or proteases has been shown in several cases, with differences in degradation rates expectedly varying dependent on sequence and position of the D-amino acid(s), as well as conditions applied [19]. From a medicinal perspective, inert bulking agents have value, however a greater advantage comes when the increased stability is coupled to a therapeutic or diagnostic use, such as the delivery of drugs or imaging agents in vivo [15].…”
Section: Introductionmentioning
confidence: 99%
“…These results underscore a new opportunity for systematic exploration of the self-assembly of small biomolecules by varying any individual segment to generate a large array of supramolecular hydrogels for biological functions and for biomedical applications. [165] …”
Section: Supramolecular Hydrogels Made Of the Hybrids Of Basic Biomentioning
confidence: 99%