Morphological characterization of elastin-mimetic block copolymers utilizing cryo- and cryoetch-HRSEM
- PMID: 12807669
- DOI: 10.1017/S1431927603030150
Morphological characterization of elastin-mimetic block copolymers utilizing cryo- and cryoetch-HRSEM
Erratum in
- Microsc Microanal. 2003 Aug;9(4):376
Abstract
Elastin-mimetic block copolymers were produced by genetic engineering. Genetically driven synthesis permitted control of the final physiochemical characteristics of the block copolymers. We designed BB and BAB block copolymers in which the A-block was hydrophilic and the B-block was hydrophobic. By designing the copolymers in this manner, it was proposed that they would self-assemble into micellar aggregates that, at high concentration, would form thermoreversible hydrogels. To analyze the three-dimensional fine surface morphology of the copolymers, to the resolution level of a few nanometers, we employed cryo-HRSEM. This method provided vast expanses of the specimen in its frozen hydrated state for survey. In our initial cryo-HRSEM studies, we observed the protein filaments and micelles surrounded by lakes of vitreous ice. Upon examination at low and intermediate magnifications, there was an extensive honeycomb-like filamentous network. To delineate the fine morphology of the hydrogel network at high magnification and to greater depths, we cryoetched away unbound water from the sample surface, in high vacuum, prior to chromium deposition. By using this technique, we were able to visualize for characterization purposes the fine fibril networks formed from the micellar aggregates over the surface of the hydrogel.
Similar articles
-
Self-assembly of block copolymers derived from elastin-mimetic polypeptide sequences.Adv Drug Deliv Rev. 2002 Oct 18;54(8):1057-73. doi: 10.1016/s0169-409x(02)00059-5. Adv Drug Deliv Rev. 2002. PMID: 12384307 Review.
-
In-lens cryo-high resolution scanning electron microscopy: methodologies for molecular imaging of self-assembled organic hydrogels.Microsc Microanal. 2003 Aug;9(4):286-95. doi: 10.1017/S1431927603030551. Microsc Microanal. 2003. PMID: 12901763
-
In-situ formation of biodegradable hydrogels by stereocomplexation of PEG-(PLLA)8 and PEG-(PDLA)8 star block copolymers.Biomacromolecules. 2006 Oct;7(10):2790-5. doi: 10.1021/bm060630e. Biomacromolecules. 2006. PMID: 17025354
-
Viscoelastic and mechanical behavior of recombinant protein elastomers.Biomaterials. 2005 Aug;26(23):4695-706. doi: 10.1016/j.biomaterials.2004.11.027. Biomaterials. 2005. PMID: 15763249
-
Recombinant elastin-mimetic biomaterials: Emerging applications in medicine.Adv Drug Deliv Rev. 2010 Dec 30;62(15):1468-78. doi: 10.1016/j.addr.2010.04.007. Epub 2010 May 2. Adv Drug Deliv Rev. 2010. PMID: 20441783 Free PMC article. Review.
Cited by
-
A permanent change in protein mechanical responses can be produced by thermally-induced microdomain mixing.J Biomater Sci Polym Ed. 2009;20(11):1629-44. doi: 10.1163/156856208X386228. J Biomater Sci Polym Ed. 2009. PMID: 19619402 Free PMC article.
-
Cell behavior on a CCN1 functionalized elastin-mimetic protein polymer.Biomaterials. 2012 Mar;33(8):2431-8. doi: 10.1016/j.biomaterials.2011.11.055. Epub 2011 Dec 31. Biomaterials. 2012. PMID: 22212194 Free PMC article.
-
Thermoresponsive Elastin-b-Collagen-Like Peptide Bioconjugate Nanovesicles for Targeted Drug Delivery to Collagen-Containing Matrices.Biomacromolecules. 2017 Aug 14;18(8):2539-2551. doi: 10.1021/acs.biomac.7b00686. Epub 2017 Aug 1. Biomacromolecules. 2017. PMID: 28719196 Free PMC article.
-
Peptide-based Biopolymers in Biomedicine and Biotechnology.Mater Sci Eng R Rep. 2008 Jan;62(4):125-155. doi: 10.1016/j.mser.2008.04.004. Mater Sci Eng R Rep. 2008. PMID: 19122836 Free PMC article.
-
Elastomeric polypeptide-based biomaterials.J Polym Sci A Polym Chem. 2010 Oct;1(8):1160-1170. doi: 10.1039/b9py00346k. J Polym Sci A Polym Chem. 2010. PMID: 21637725 Free PMC article.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources