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Acrl peg sva

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ACRL-PEG-SVA is a heterobifunctional crosslinker that contains an N-hydroxysuccinimide (NHS) ester and an acrylate group. It can be used to conjugate biomolecules such as proteins, peptides, and small molecules.

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4 protocols using acrl peg sva

1

Covalent Linkage of Scl2-2 Protein in PEGDA Hydrogels

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In order to covalently link the Scl2-2 protein into the structure of PEGDA hydrogels, the Scl2-2 protein was acrylate-derivatized using PEG-succinimidyl valerate (ACRL-PEG-SVA, 3.4 kDa; Laysan Bio). Briefly, Scl2-2 trimer and ACRL-PEG-SVA were reacted at a molar ratio of 1:6 for 2 h in phosphate buffered saline (PBS, pH 7.4; Life Technologies). Immediately following the derivation reaction, the resulting ACRL-PEG-Scl2-2 product was used for the fabrication of the PEG-Scl2-2 hydrogels. As a control, rat tail collagen I (Life Technologies) was also reacted with ACRL-PEG-SVA for 2 h at a 1:6 molar ratio in 50 mM sodium bicarbonate buffer, pH 8.5.70 (link) The resulting products were then dialyzed against double deionized water for 48 h. Following purification, the acrylate-derivatized collagen was lyophilized and stored at -80 ºC until use. The incorporation of acrylate groups within the Scl2-2 and collagen I was confirmed by Fourier Transform Infrared Spectroscopy following previously described methods.57 (link) Both acrylate-derivatized and unmodified Scl2-2 were also analyzed by circular dichroism as previously described.57 (link) Results from the circular dichroism analyses are shown in Supplementary Figure 1.
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2

Synthetic Peptide Conjugation for Biomaterials

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The GF binding peptides, KGLPLGNSH [19 (link)] (Genscript, Piscataway, NJ, USA), targeting the human Transforming Growth Factor beta 1 (hTGFβ1), and DRVQRQTTTVVA [20 (link)] (Genscript), targeting the human Vascular Endothelial Growth Factor (hVEGF), and the cell adhesion peptide, RGDS (Genscript), were conjugated to Acrylate-PEG-Succinimidyl Valerate (ACRL-PEG-SVA 3.4 kDa, Laysan Bio, Arab, AL, USA). The peptides were dissolved in a 50 mM NaHCO3 pH 8.5 buffer and reacted with ACRL-PEG-SVA at a 1:1 molar ratio for 2 h. The products (ACRL-PEG-KGLPLGNSH, ACRL-PEG-DRVQRQTTTVVA and ACRL-PEG-RGDS) were purified through a dialysis membrane (3.5 kDa, Thermo Fisher Scientific, Waltham, MA, USA) for 24 h and then lyophilized. The products were stored at −20 °C until further use. Peptide conjugation to ACRL-PEG-SVA was confirmed using ATR-FTIR.
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3

Functionalization of Growth Factors and Peptide

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Addition of acryl groups to RGDS (American Peptide), human recombinant carrier free BMP2 (R&D systems), and human recombinant carrier free TGFβ1 (EMD Millipore) was carried out via reaction with acryloyl-PEG-succinimidyl valerate (ACRL-PEG-SVA, 3.4 kDa; Laysan Bio) at a 1:1 molar ratio for RGDS or 1:6 molar ratio for BMP2 and TGFβ1. Reconstituted TGFβ1 and BMP2 were first dialyzed to non-growth factor associated primary amines. The resulting mixtures were reacted for 2 hr in 50 mM sodium bicarbonate buffer, pH 8.5.74 ,75 The ACRL-PEG-RGDS was purified by dialysis overnight against dIH2O at 4°C using 3500 MWCO Snakeskin Dialysis tubing (Thermo Fisher Scientific) to remove unreacted ACRL-PEG-SVA. ACRL-PEG-BMP2 and ACRL-PEGTGFβ1 were purified by dialysis overnight against dIH2O at 4°C using 5000 MWCO Snakeskin Dialysis tubing.
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4

Acrylate Derivatization of Scl2-2 and Collagen for Hydrogel Fabrication

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Following expression and purification, the Scl2-2 protein was acrylate-derivatized in order to permit its chemical conjugation within PEG diacrylate hydrogels. Briefly, Scl2-2 was reacted with acrylate-PEG-succinimidyl valerate (ACRL-PEG-SVA, 3.4 kDa; Laysan Bio, Inc.) at a molar ratio of 1:6 for 2 h in Dulbecco's phosphate buffered saline (DPBS, pH 7.4; Life Technologies). The resulting acrylate-derivatized protein was used immediately for the fabrication of PEG-Scl2-2 hydrogels. In a similar manner, collagen I (rat tail, Life Technologies) was reacted with ACRL-PEG-SVA at a 1:6 molar ratio for 2 h in 50 mM sodium bicarbonate buffer, pH 8.5.27 The resulting acrylate-derivatized collagen was purified by dialysis against double deionized water, lyophilized and stored at -20 °C until use. Acrylation of the Scl2-2 protein and collagen was confirmed using Fourier Transform Infrared Spectroscopy as previously described.20 (link)
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