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Controllably degradable ?-sheet nanofibers and gels from self-assembling depsipeptides.


ABSTRACT: Self-assembled peptide materials have received considerable interest for a range of applications, including 3D cell culture, tissue engineering, and the delivery of cells and drugs. One challenge in applying such materials within these areas has been the extreme stability of ?-sheet fibrillized peptides, which are resistant to proteolysis, degradation, and turnover in biological environments. In this study, we designed self-assembling depsipeptides containing ester bonds within the peptide backbone. Beta-sheet fibrillized nanofibers were formed in physiologic conditions, and two of these nanofiber-forming depsipeptides produced hydrogels that degraded controllably over the course of days-to-weeks via ester hydrolysis. With HPLC, TEM, and oscillating rheometry, we show that the rate of hydrolysis can be controlled in a straightforward manner by specifying the amino acid residues surrounding the ester bond. In 3D cell cultures, depsipeptide gels softened over the course of several days and permitted considerably more proliferation and spreading of C3H10T1/2 pluripotent stem cells than non-degradable analogs. This approach now provides a reliable and reproducible means to soften or clear ?-sheet fibrillized peptide materials from biological environments.

SUBMITTER: Tian YF 

PROVIDER: S-EPMC3819105 | biostudies-literature | 2013 Oct

REPOSITORIES: biostudies-literature

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Controllably degradable β-sheet nanofibers and gels from self-assembling depsipeptides.

Tian Ye F YF   Hudalla Gregory A GA   Han Huifang H   Collier Joel H JH  

Biomaterials science 20131001 10


Self-assembled peptide materials have received considerable interest for a range of applications, including 3D cell culture, tissue engineering, and the delivery of cells and drugs. One challenge in applying such materials within these areas has been the extreme stability of β-sheet fibrillized peptides, which are resistant to proteolysis, degradation, and turnover in biological environments. In this study, we designed self-assembling depsipeptides containing ester bonds within the peptide backb  ...[more]

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