Three-dimensional Immobilization of Proteins within Agarose Hydrogels using Two-photon Chemistry

Three-dimensional biomolecule patterned hydrogels provide cellular microenvironments that mimic in vivo conditions. We are particularly interested in the fabrication of materials to spatially control stem cell differentiation towards the creation of tissue analogues. To this end, we have designed a...

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Main Author: Wylie, Ryan Gavin
Other Authors: Shoichet, Molly
Language:en_ca
Published: 2011
Subjects:
Online Access:http://hdl.handle.net/1807/31977
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spelling ndltd-TORONTO-oai-tspace.library.utoronto.ca-1807-319772013-11-08T04:03:47ZThree-dimensional Immobilization of Proteins within Agarose Hydrogels using Two-photon ChemistryWylie, Ryan Gavin3D patterningProtein immobilization0541Three-dimensional biomolecule patterned hydrogels provide cellular microenvironments that mimic in vivo conditions. We are particularly interested in the fabrication of materials to spatially control stem cell differentiation towards the creation of tissue analogues. To this end, we have designed a 3D protein patterning system where differentiation factors were immobilized within distinct volumes through two-photon chemistry, which provides 3D control since the excitation volume is limited to the focal point of the laser. Agarose hydrogels were modified with 6-bromo-7-hydroxy-coumarin (Bhc) protected amines or thiols, which upon two-photon excitation are deprotected in defined volumes yielding reactive amines or thiols. Fibroblast growth factor-2 (FGF-2) was immobilized onto agarose-thiol-Bhc through either disulfide bond formation with agarose thiols or the physical interaction between human serum albumin (HSA) and the albumin binding domain (ABD). The use of biological binding pairs also provides mild immobilization conditions, minimizing the risk for bioactivity loss. Similarly, two differentiation factors for retinal stem progenitor cells were simultaneously immobilized: 1) ciliary neurotrophic factor (CNTF); and 2) N-terminal sonic hedgehog (SHH). Maleimide modified binding proteins, such as maleimide-streptavidin; react with exposed thiols, yielding 3D patterns of covalently immobilized streptavidin in agarose hydrogels. Growth factors are then introduced as fusion proteins with binding domains, such as biotin-CNTF, for complexation and thus 3D immobilization. By combining multiple binding systems with two-photon patterning, we were able to simultaneously 3D immobilize proteins towards the creation biomimetic hydrogels.Shoichet, Molly2011-112012-01-12T16:08:20ZNO_RESTRICTION2012-01-12T16:08:20Z2012-01-12Thesishttp://hdl.handle.net/1807/31977en_ca
collection NDLTD
language en_ca
sources NDLTD
topic 3D patterning
Protein immobilization
0541
spellingShingle 3D patterning
Protein immobilization
0541
Wylie, Ryan Gavin
Three-dimensional Immobilization of Proteins within Agarose Hydrogels using Two-photon Chemistry
description Three-dimensional biomolecule patterned hydrogels provide cellular microenvironments that mimic in vivo conditions. We are particularly interested in the fabrication of materials to spatially control stem cell differentiation towards the creation of tissue analogues. To this end, we have designed a 3D protein patterning system where differentiation factors were immobilized within distinct volumes through two-photon chemistry, which provides 3D control since the excitation volume is limited to the focal point of the laser. Agarose hydrogels were modified with 6-bromo-7-hydroxy-coumarin (Bhc) protected amines or thiols, which upon two-photon excitation are deprotected in defined volumes yielding reactive amines or thiols. Fibroblast growth factor-2 (FGF-2) was immobilized onto agarose-thiol-Bhc through either disulfide bond formation with agarose thiols or the physical interaction between human serum albumin (HSA) and the albumin binding domain (ABD). The use of biological binding pairs also provides mild immobilization conditions, minimizing the risk for bioactivity loss. Similarly, two differentiation factors for retinal stem progenitor cells were simultaneously immobilized: 1) ciliary neurotrophic factor (CNTF); and 2) N-terminal sonic hedgehog (SHH). Maleimide modified binding proteins, such as maleimide-streptavidin; react with exposed thiols, yielding 3D patterns of covalently immobilized streptavidin in agarose hydrogels. Growth factors are then introduced as fusion proteins with binding domains, such as biotin-CNTF, for complexation and thus 3D immobilization. By combining multiple binding systems with two-photon patterning, we were able to simultaneously 3D immobilize proteins towards the creation biomimetic hydrogels.
author2 Shoichet, Molly
author_facet Shoichet, Molly
Wylie, Ryan Gavin
author Wylie, Ryan Gavin
author_sort Wylie, Ryan Gavin
title Three-dimensional Immobilization of Proteins within Agarose Hydrogels using Two-photon Chemistry
title_short Three-dimensional Immobilization of Proteins within Agarose Hydrogels using Two-photon Chemistry
title_full Three-dimensional Immobilization of Proteins within Agarose Hydrogels using Two-photon Chemistry
title_fullStr Three-dimensional Immobilization of Proteins within Agarose Hydrogels using Two-photon Chemistry
title_full_unstemmed Three-dimensional Immobilization of Proteins within Agarose Hydrogels using Two-photon Chemistry
title_sort three-dimensional immobilization of proteins within agarose hydrogels using two-photon chemistry
publishDate 2011
url http://hdl.handle.net/1807/31977
work_keys_str_mv AT wylieryangavin threedimensionalimmobilizationofproteinswithinagarosehydrogelsusingtwophotonchemistry
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