Literature DB >> 29637775

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

Tugce Nihal Gevrek, Merve Cosar, Duygu Aydin, Elif Kaga, Mehmet Arslan, Rana Sanyal, Amitav Sanyal.   

Abstract

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 groups as thiol-reactive handles were prepared by photopolymerization in the presence of a poly(ethylene glycol) (PEG)-based cross-linker. A range of bulk and micropatterned 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 4,4-difluoro-1,3,5,7-tetramethyl-8-[(10-mercapto)]-4-bora-3 a,4 a-diaza- s-indacene, 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 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 a 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.

Entities:  

Keywords:  bioconjugation; hydrogel interfaces; protein and cell attachment; reversible conjugation; thiol−disulfide exchange chemistry

Mesh:

Substances:

Year:  2018        PMID: 29637775     DOI: 10.1021/acsami.8b00802

Source DB:  PubMed          Journal:  ACS Appl Mater Interfaces        ISSN: 1944-8244            Impact factor:   9.229


  5 in total

1.  Redox-Responsive Hydrogels for Tunable and "On-Demand" Release of Biomacromolecules.

Authors:  Ruveyda Kilic Boz; Duygu Aydin; Salli Kocak; Bianka Golba; Rana Sanyal; Amitav Sanyal
Journal:  Bioconjug Chem       Date:  2022-04-21       Impact factor: 6.069

Review 2.  Chemical Conjugation Strategies for the Development of Protein-Based Subunit Nanovaccines.

Authors:  Lantian Lu; Viet Tram Duong; Ahmed O Shalash; Mariusz Skwarczynski; Istvan Toth
Journal:  Vaccines (Basel)       Date:  2021-05-28

3.  Differentiating Co-Delivery of Bisphosphonate and Simvastatin by Self-Healing Hyaluronan Hydrogel Formed by Orthogonal "Clicks": An In-Vitro Assessment.

Authors:  Dmitri A Ossipov; Mads Lüchow; Michael Malkoch
Journal:  Polymers (Basel)       Date:  2021-06-26       Impact factor: 4.329

4.  A Modular and Practical Synthesis of Zwitterionic Hydrogels through Sequential Amine-Epoxy "Click" Chemistry and N-Alkylation Reaction.

Authors:  Junki Oh; Kevin Injoe Jung; Hyun Wook Jung; Anzar Khan
Journal:  Polymers (Basel)       Date:  2019-09-12       Impact factor: 4.329

5.  Vapor-Deposited Reactive Coating with Chemically and Topographically Erasable Properties.

Authors:  Yu-Chih Chiang; Cuei-Ping Ho; Yin-Lin Wang; Po-Chun Chen; Peng-Yuan Wang; Hsien-Yeh Chen
Journal:  Polymers (Basel)       Date:  2019-09-29       Impact factor: 4.329

  5 in total

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