Interfacial Bioorthogonal Cross-Linking
Open Access
- 14 July 2014
- journal article
- letter
- Published by American Chemical Society (ACS) in ACS Macro Letters
- Vol. 3 (8), 727-731
- https://doi.org/10.1021/mz5002993
Abstract
Described herein is interfacial bioorthogonal cross-linking, the use of bioorthogonal chemistry to create and pattern biomaterials through diffusion-controlled gelation at the liquid-gel interface. The basis is a rapid (k2 284000 M–1 s–1) reaction between strained trans-cyclooctene (TCO) and tetrazine (Tz) derivatives. Syringe delivery of Tz-functionalized hyaluronic acid (HA-Tz) to a bath of bis-TCO cross-linker instantly creates microspheres with a cross-linked shell through which bis-TCO diffuses freely to introduce further cross-linking at the interface. Tags can be introduced with 3D resolution without external triggers or templates. Water-filled hydrogel channels were prepared by simply reversing the order of addition. Prostate cancer cells encapsulated in the microspheres have 99% viability, proliferate readily, and form aggregated clusters. This process is projected to be useful in the fabrication of cell-instructive matrices for in vitro tissue models.Keywords
Funding Information
- National Institutes of Health (COBRE 2P20RR017716, NIDCR, R01 DE022969, NIH S10 RR026962)
- National Science Foundation (CHE0840401, CHE1229234, DMR1206310)
This publication has 43 references indexed in Scilit:
- Synthetically Tractable Click Hydrogels for Three-Dimensional Cell Culture Formed Using Tetrazine–Norbornene ChemistryBiomacromolecules, 2013
- Genetic Encoding of Bicyclononynes and trans-Cyclooctenes for Site-Specific Protein Labeling in Vitro and in Live Mammalian Cells via Rapid Fluorogenic Diels–Alder ReactionsJournal of the American Chemical Society, 2012
- Biomedical Applications of Tetrazine CycloadditionsAccounts of Chemical Research, 2011
- Design and Synthesis of Highly Reactive Dienophiles for the Tetrazine–trans-Cyclooctene LigationJournal of the American Chemical Society, 2011
- High‐Yielding, Two‐Step 18F Labeling Strategy for 18F‐PARP1 InhibitorsChemMedChem, 2011
- Formation of Three-Dimensional Hydrogel Multilayers Using Enzyme-Mediated Redox Chain InitiationACS Applied Materials & Interfaces, 2010
- Bioorthogonal Chemistry: Fishing for Selectivity in a Sea of FunctionalityAngewandte Chemie International Edition, 2009
- Tetrazine-Based Cycloadditions: Application to Pretargeted Live Cell ImagingBioconjugate Chemistry, 2008
- Tetrazine Ligation: Fast Bioconjugation Based on Inverse-Electron-Demand Diels−Alder ReactivityJournal of the American Chemical Society, 2008
- 3-D Tissue Culture Systems for the Evaluation and Optimization of Nanoparticle-Based Drug CarriersBioconjugate Chemistry, 2008