Enzyme‐Responsive Delivery of Multiple Proteins with Spatiotemporal Control
Source abstract
Abstract
Orchestrated biological materials such as enzymes and growth factors regulate the growth of tissues and organs. A chirality-controlled, single-protein technology is devised to tailor the spatiotemporally defined delivery of therapeutic proteins in response to natural enzymes present at wound sites. Sustained delivery of one protein and sequential delivery of two proteins are demonstrated for stroke and skin wound healing. As a service to our authors and readers, this journal provides supporting information supplied by the authors. Such materials are peer reviewed and may be re-organized for online delivery, but are not copy-edited or typeset. Technical support issues arising from supporting information (other than missing files) should be addressed to the authors. Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Electrospun Nanofibers in Biomedical Applications · Nanoparticle-Based Drug Delivery · Polymer Surface Interaction Studies
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Chemical and Biomolecular Engineering University of California Los Angeles, 420 Westwood Plaza Los Angeles CA 90095 USA
Department of Neurology David Geffen School of Medicine University of California Los Angeles, 710 Westwood Plaza Los Angeles CA 90095 USA
Funding
American Heart Association · National Institutes of Health · NSF
References (23)
Show source-provided references
1. 10.1038/nrd239910.1038/nrd2399 ↗
2. 10.1038/nature0703910.1038/nature07039 ↗
3. 10.1111/j.1440-0960.1994.tb01799.x10.1111/j.1440-0960.1994.tb01799.x ↗
4. 10.1002/anie.20140370210.1002/anie.201403702 ↗
5. 10.1016/j.biomaterials.2011.07.02210.1016/j.biomaterials.2011.07.022 ↗
6. 10.1038/nbt1101-102910.1038/nbt1101-1029 ↗
7. 10.1016/j.jconrel.2013.07.03210.1016/j.jconrel.2013.07.032 ↗
8. 10.1002/jbm.a.2009110.1002/jbm.a.20091 ↗
9. 10.1002/adma.20110177110.1002/adma.201101771 ↗
10. 10.1038/nbt.210810.1038/nbt.2108 ↗
11. 10.1038/nnano.2009.34110.1038/nnano.2009.341 ↗
12. 10.1097/01.ASW.0000418541.31366.a310.1097/01.ASW.0000418541.31366.a3 ↗
13. 10.1016/j.biomaterials.2013.06.06110.1016/j.biomaterials.2013.06.061 ↗
14. 10.1016/S0022-5223(95)70188-510.1016/S0022-5223(95)70188-5 ↗
15. 10.1172/JCI1842010.1172/JCI18420 ↗
16. 10.1096/fj.06-6568fje10.1096/fj.06-6568fje ↗
17. 10.1016/S0002-9440(10)63754-610.1016/S0002-9440(10)63754-6 ↗
18. Greenhalgh D. G. · Am. J. Pathol. · 1990 · 136 · 1235
19. 10.1172/JCI936910.1172/JCI9369 ↗
20. 10.1002/jnr.2308810.1002/jnr.23088 ↗
21. 10.1046/j.1524-475X.1999.00154.x10.1046/j.1524-475X.1999.00154.x ↗
22. 10.1074/jbc.270.21.1260710.1074/jbc.270.21.12607 ↗
23. 10.1038/nm.366810.1038/nm.3668 ↗