Compositions and methods for rapid and reversible biomolecular labeling
US-2024426816-A1 · Dec 26, 2024 · US
US9927334B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9927334-B2 |
| Application number | US-201213982680-A |
| Country | US |
| Kind code | B2 |
| Filing date | Feb 3, 2012 |
| Priority date | Feb 3, 2011 |
| Publication date | Mar 27, 2018 |
| Grant date | Mar 27, 2018 |
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Disclosed herein are hydrogel compositions and methods of making hydrogel compositions. Furthermore, methods of specifically capturing and releasing biological materials from a sample using the disclosed hydrogel compositions are disclosed, including methods of utilizing the compositions in microfluidic devices.
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The invention claimed is: 1. A hydrogel composition comprising: a plurality of alginic acid molecules; divalent cations crosslinking the alginic acid molecules; a plurality of branched polyethylene glycol molecules comprising a plurality of attachment points; and one or more binding agents, wherein the alginic acid molecules are conjugated to the branched polyethylene glycol molecules by a first of the attachment points, and the one or more binding agents are conjugated to the branched polyethylene glycol molecules by a second of the attachment points, and wherein the hydrogel composition dissolves in the presence of a chelator. 2. The composition of claim 1 , wherein the branched polyethylene glycol molecules are four-arm molecules. 3. The composition of claim 1 , wherein the one or more binding agents is an antibody, antibody fragment, peptidomimetic compound, peptide, small molecule, or nucleic acid. 4. The composition of claim 3 , wherein the antibody is selected from the group consisting of antibodies against GPR49, LGR5, CD24, FLK1, CD45, CD31, CD34, and sca-1 proteins. 5. A method of capturing and releasing target biological materials from a sample, the method comprising: (a) providing a microfluidic device comprising one or more chambers for receiving fluids, wherein at least one of the one or more chambers comprises a surface coated with a hydrogel composition, the hydrogel composition comprising: a plurality of alginic acid molecules; divalent cations crosslinking the alginic acid molecules; branched polyethylene glycol molecules comprising a plurality of attachment points; and one or more binding agents that bind to the target biological materials; wherein the alginic acid molecules are conjugated to the branched polyethylene glycol molecules by a first of the attachment points, and the one or more binding agents are conjugated to the branched polyethylene glycol molecules by a second of the attachment points, and wherein the hydrogel composition dissolves in the presence of a chelator; (b) introducing the sample comprising target and non-target biological materials into the one or more chambers under conditions effective to bind the target biological materials to the hydrogel composition; and (c) releasing the target biological materials using a chelator. 6. The method of claim 5 , further comprising removing the unbound non-target materials from the sample prior to step (c). 7. A method of making a hydrogel composition, the method comprising: (a) reacting branched polyethylene glycol molecules comprising a plurality of attachment points with one or more binding agents in a buffer; and (b) reacting the branched polyethylene glycol binding agent solution with alginic acid molecules and divalent cations to form a functionalized hydrogel, the functionalized hydrogel comprising branched polyethylene glycol molecules conjugated at least one alginic acid molecule by a first of the attachment points and further conjugated to one or more binding agents by a second of the attachment points, wherein the hydrogel composition dissolves in the presence of a chelator. 8. The method of claim 7 , wherein the polyethylene glycol molecule is a four-arm molecule. 9. The method of claim 7 , wherein the one or more binding agents is an antibody, antibody fragment, peptidomimetic compound, peptide, small molecule, or a nucleic acid. 10. The method of claim 9 , wherein the antibody is selected from the group consisting of antibodies against GPR49, LGR5, CD24, FLK1, CD45, CD31, CD34, and sca-1 proteins. 11. The hydrogel composition of claim 1 , wherein the divalent cations are Ca 2+ cations. 12. The method of claim 5 , wherein the divalent cations are Ca 2+ cations. 13. The method of claim 7 , wherein the divalent cations are Ca 2+ cations.
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