Next Article in Journal
Clinicopathological Significance of NMIIA Overexpression in Human Gastric Cancer
Previous Article in Journal
Role of Oxidative Stress in Hepatocarcinogenesis Induced by Hepatitis C Virus
Article Menu

Export Article

Open AccessArticle
Int. J. Mol. Sci. 2012, 13(11), 15279-15290; doi:10.3390/ijms131115279

Molecular Mechanisms of RADA16-1 Peptide on Fast Stop Bleeding in Rat Models

1
Institute for NanoBiomedical Technology and Membrane Biology, West China Hospital, Sichuan University, Chengdu 610041, Sichuan, China
2
College of Life Science, Jianghan University, Wuhan 430056, Hubei, China
3
National Engineering Research Center for solid state fermentation, Luzhou 640040, Sichuan, China
*
Author to whom correspondence should be addressed.
Received: 13 July 2012 / Revised: 8 November 2012 / Accepted: 12 November 2012 / Published: 19 November 2012
(This article belongs to the Section Biochemistry, Molecular Biology and Biophysics)
View Full-Text   |   Download PDF [2789 KB, uploaded 19 June 2014]   |  

Abstract

Ionic self-assembly of the peptide RADARADARADARADA (RADA16-1) may form a well-defined nanofiber and eventually a hydrogel scaffold, with a water content of over 99.5%. This leads to the establishment of a nanofiber barrier that can be used to achieve complete hemostasis in less than 20 s in multiple tissues and in a variety of different wounds. In the present study, the nanofiber scaffolds of RADA16-1 peptide were sonicated into smaller fragments to identify possible molecular mechanisms underlying the rapid cessation of bleeding associated with these materials. Atomic force microscopy (AFM), circular dichroism (CD), and rheometry were also used to evaluate the re-assembly kinetics of this peptide. A bleeding control experiment was performed in animal models to uncover the molecular mechanisms underlying this fast hemostasis. In this way, these sonicated fragments not only quickly reassembled into nanofibers indistinguishable from the original material, but the degree of reassembly was also correlated with an increase in the rigidity of the scaffold and increased as the time required for hemostasis increased.
Keywords: RADA16-1; nanofiber scaffolds; self-assembly; hemostasis RADA16-1; nanofiber scaffolds; self-assembly; hemostasis
This is an open access article distributed under the Creative Commons Attribution License (CC BY 3.0).

Scifeed alert for new publications

Never miss any articles matching your research from any publisher
  • Get alerts for new papers matching your research
  • Find out the new papers from selected authors
  • Updated daily for 49'000+ journals and 6000+ publishers
  • Define your Scifeed now

SciFeed Share & Cite This Article

MDPI and ACS Style

Wang, T.; Zhong, X.; Wang, S.; Lv, F.; Zhao, X. Molecular Mechanisms of RADA16-1 Peptide on Fast Stop Bleeding in Rat Models. Int. J. Mol. Sci. 2012, 13, 15279-15290.

Show more citation formats Show less citations formats

Related Articles

Article Metrics

Article Access Statistics

1

Comments

[Return to top]
Int. J. Mol. Sci. EISSN 1422-0067 Published by MDPI AG, Basel, Switzerland RSS E-Mail Table of Contents Alert
Back to Top