Facile Fabrication of a Modular 'Catch and Release' Hydrogel Interface: Harnessing Thiol-Disulfide Exchange for Reversible Protein Capture and Cell Attachment.

Surfaces engineered to 'specifically capture' and 'release on demand' analytes ranging from biomolecules to cells find niche applications in areas such as diagnostics and detection. Utilization of a disulfide-based linker as a building block allows fabrication of a novel hydrogel based platform that incorporates a 'catch and release' attribute. Hydrogels incorporating pyridyl disulfide group as a thiol-reactive handle were prepared by photopolymerization in presence of a PEG-based crosslinker. A range of bulk and micro-patterned hydrogels with varying amounts of the reactive group were prepared using PEG-based monomers with different chain lengths. Thiol-containing molecules were conjugated to these hydrogels through the thiol-disulfide exchange reaction under ambient conditions with high efficiencies, as determined by UV-vis spectroscopy. Facile conjugation of a thiol-containing fluorescent dye, namely BODIPY-SH, was demonstrated, followed by its effective cleavage in the presence of dithiothreitol (DTT), a thiol-containing disulfide reducing agent. Conjugation of a biotin-containing ligand onto the hydrogels allowed specific binding of the protein extravidin when exposed to a mixture of extravidin and bovine serum albumin. The bound protein could be released from the hydrogel by simple exposure to a DTT solution. Likewise, hydrogels modified with a cell adhesive peptide unit containing the RGD-sequence acted as favorable substrates for cellular attachment. Incubation of these cell attached hydrogel surfaces in a DTT-containing solution leads to facile detachment of cells from the surfaces, while retaining high level of cell viability. It can be envisioned that the benign nature of these hydrogels, their facile fabrication and modular functionalization will make them attractive platforms for many applications.