Synthesis of bioactive protein hydrogels by genetically encoded SpyTag-SpyCatcher chemistry
Abstract
Protein-based hydrogels have emerged as promising alternatives to synthetic hydrogels for biomedical applications, owing to the precise control of structure and function enabled by protein engineering. Nevertheless, strategies for assembling 3D molecular networks that carry the biological information encoded in full-length proteins remain underdeveloped. Here we present a robust protein gelation strategy based on a pair of genetically encoded reactive partners, SpyTag and SpyCatcher, that spontaneously form covalent isopeptide linkages under physiological conditions. The resulting "network of Spies" may be designed to include cell-adhesion ligands, matrix metalloproteinase-1 cleavage sites, and full-length globular proteins [mCherry and leukemia inhibitory factor (LIF)]. The LIF network was used to encapsulate mouse embryonic stem cells; the encapsulated cells remained pluripotent in the absence of added LIF. These results illustrate a versatile strategy for the creation of information-rich biomaterials.
Additional Information
Copyright © 2014 National Academy of Sciences. Edited by Robert Langer, Massachusetts Institute of Technology, Cambridge, MA, and approved July 1, 2014 (received for review January 21, 2014). Published ahead of print July 21, 2014. This research was funded by National Science Foundation Grant DMR 1206121 and by the Gordon and Betty Moore Foundation through Grant GBMF2809 to the California Institute of Technology Programmable Molecular Technology Initiative. F.S. and W.-B.Z. contributed equally to this work. Author contributions: F.S., W.-B.Z., F.H.A., and D.A.T. designed research; F.S., W.-B.Z., and A.M. performed research; F.S., W.-B.Z., and A.M. contributed new reagents/analytic tools; F.S., W.-B.Z., A.M., F.H.A., and D.A.T. analyzed data; and F.S., W.-B.Z., A.M., F.H.A., and D.A.T. wrote the paper. The authors declare no conflict of interest. This article is a PNAS Direct Submission. This article contains supporting information online at www.pnas.org/lookup/suppl/doi:10.1073/pnas.1401291111/-/DCSupplemental.Attached Files
Published - 11269.full.pdf
Supplemental Material - pnas.1401291111.sapp.pdf
Files
Name | Size | Download all |
---|---|---|
md5:4e219d7a473dfa939dd6a3bddf6b347f
|
1.1 MB | Preview Download |
md5:77b2aa97bd949037df7cf0ea27038171
|
772.9 kB | Preview Download |
Additional details
- PMCID
- PMC4128157
- Eprint ID
- 47388
- DOI
- 10.1073/pnas.1401291111
- Resolver ID
- CaltechAUTHORS:20140722-093927552
- DMR-1206121
- NSF
- GBMF2809
- Gordon and Betty Moore Foundation
- Created
-
2014-07-22Created from EPrint's datestamp field
- Updated
-
2021-11-10Created from EPrint's last_modified field