期刊
BIOMATERIALS
卷 32, 期 8, 页码 2013-2020出版社
ELSEVIER SCI LTD
DOI: 10.1016/j.biomaterials.2010.11.049
关键词
Chirality; Circular dichroism; D-form amino acids; Molecular self-assembly; Scaffold hydrogel
资金
- Sichuan University
We previously reported a class of designer self-assembling peptides that form 3-dimensional nanofiber scaffolds using only L-amino acids. Here we report that using D-amino acids, the chiral self-assembling peptide d-EAK16 also forms 3-dimensional nanofiber scaffold that is indistinguishable from its counterpart l-EAK16. These chiral peptides containing all D-amino acids, d-EAK16, self-assemble into well-ordered nanofibers. However with alternating D- and L-amino acids, EA*K16 and E*AK*16, showed poor self-assembling properties. To fully understand individual molecular building blocks and their structures, assembly properties and dynamic behaviors for rapid hemostasis, we used circular dichroism, atomic force microscopy and scanning electron microscopy to study in detail the peptides. We also used rheological measurement to study the hydrogel gelation property. Furthermore, we used an erythrocyte-agglutination test and a rabbit liver wound healing model, particularly in the transverse rabbit liver experiments, to examine rapid hemostasis. We showed that 1% d-EAK16 for the liver wound hemostasis took similar to 20 s, but using 1% of E*A*K16 and EA*K16 that have alternating chiral D- and L-amino acids took similar to 70 and similar to 80 s, respectively. We here propose a plausible model not only to provide insights in understanding the chiral assembly properties for rapid hemostasis, but also to aid in further design of self-assembling is-form peptide scaffolds for clinical applications. (C)2010 Elsevier Ltd. All rights reserved.
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