Modified substrates for protection of peptide-immobilized surfaces from gamma radiation degradation

Patent metadata

Field	Value
Publication number	US-10144914-B2
Application number	US-201113032166-A
Country	US
Kind code	B2
Filing date	Feb 22, 2011
Priority date	Feb 23, 2010
Publication date	Dec 4, 2018
Grant date	Dec 4, 2018

Abstract

In the present specification and claims, three modified cell culture substrates are disclosed for protecting peptide mimetic surfaces used in cell culture technology. The methods are able to retain the functionality of the bioactive species conjugated to the surface. In particular, a vitronectin peptide fragment Ac-Lys-Gly-Gly-Pro-Gln-Val-Thr-Arg-Gly-Asp-Val-Phe-Thr-Met-Pro-NH2 was able to facilitate growth and proliferation of undifferentiated human embryonic stem cells after stabilization using 3 different modified cell culture substrates for of protection against gamma irradiation. The modified substrates disclosed in this invention are (i) covalent attachment of the antioxidant molecules (via blocking step); (ii) The use of coatings consisting of anti-oxidants and stabilizers comprising glycoprotiens, sugars, carbohydrates, poly(amino acids), peptides and hydrophilic polymers; and (iii) a third method wherein the same methionine contained in the bioactive sequence used to facilitate growth and proliferation of human embryonic stem cells was also used as a sacrificial coating to protect the same conjugated sequence against damage by gamma irradiation.

First claim

We claim:

1. A cell culture substrate modified to protect and stabilize against degradation by gamma irradiation, said cell culture substrate comprising:
a cell culture surface comprising a (meth)acrylate substrate and a peptide conjugated to the (meth)acrylate substrate, wherein the (meth)acrylate substrate is formed from a composition comprising tetra(ethylene glycol) dimethacrylate, 2-hydroxyethyl methacrylate and 2-carboxyethyl acrylate; and
a methionine ester covalently bound to the cell culture surface to protect and stabilize said cell culture surface from sterilizing gamma irradiation wherein the peptide is conjugated to the (meth)acrylate substrate via an n-hydroxysuccinimide reactive group; and wherein the methionine ester is conjugated to the (meth)acrylate substrate via an n-hydroxysuccinimide reactive group.

2. The substrate of claim 1 , wherein the methionine ester is methionine methyl ester.

3. The substrate of claim 1 , wherein the methionine ester forms a protective layer having a thickness of 10 nm to 20 μM.

4. The substrate of claim 1 , wherein the peptide is a cell adhesive peptide.

5. The substrate of claim 4 , wherein the cell adhesive peptide is vitronectin.

6. The substrate of claim 5 , wherein the vitronectin has an amino acid sequence of Ac-Lys-Gly-Gly-Pro-Gln-Val-Thr-Arg-Gly-Asp-Val-Phe-Thr-Met-Pro-NH2 (SEQ ID NO: 1).

7. A method comprising:
conjugating a peptide to a (meth)acrylate substrate to form a peptide-conjugated substrate, wherein the (meth)acrylate substrate is formed from a composition comprising tetra(ethylene glycol) dimethacrylate, 2-hydroxyethyl methacrylate and 2-carboxyethyl acrylate;
conjugating a methionine ester to the peptide-conjugated substrate to form a methionine-containing peptide-conjugated substrate; and
irradiating the methionine-containing peptide-conjugated substrate with gamma radiation to sterilize the methionine-containing peptide-conjugated substrate wherein conjugating the peptide to the (meth)acrylate substrate comprises conjugating the peptide to a n-hydroxysuccinimide reactive group of the (meth)acrylate substrate; and wherein conjugating the methionine ester to the peptide-conjugated (meth)acrylate substrate comprises conjugating the methionine ester to a n-hydroxysuccinimide reactive group of the peptide-conjugated (meth)acrylate substrate.

8. The method of claim 7 , wherein conjugating the methionine ester to the peptide-conjugated substrate comprises conjugating the methionine ester to the peptide-conjugated substrate via a residual or un-reacted n-hydroxysuccinimide reactive group remaining after conjugating the peptide to the (meth)acrylate substrate.

9. The method of claim 7 , further comprising disposing the methionine ester in a solvent prior to conjugating the methionine ester to the peptide-conjugated substrate, wherein the solvent comprises one or more of lower alcohol, isopropyl alcohol, phosphate buffer solution, boric acid, or deionized water.

10. The method of claim 7 , further comprising contacting the methionine-containing peptide-conjugated substrate irradiated with gamma radiation with a surface of a cell culture article.

11. The substrate of claim 1 , wherein the methionine ester is a methionine ester salt.

12. The substrate of claim 1 , wherein the methionine ester is covalently bound to the cell culture surface via treatment of the cell culture surface with a methionine ester composition comprising methionine methyl ester hydrochloride.

13. The substrate of claim 12 , wherein the methionine ester composition consists essentially of methionine methyl ester hydrochloride.

14. The substrate of claim 1 , wherein the (meth)acrylate substrate is formed from a composition comprising a volume ratio of 2-hydroxethyl methacrylate:2-carboxyethyl acrylate:tetra(ethylene glycol) dimethacrylate of 80:20:3.

15. The substrate of claim 1 , wherein the sterilizing gamma irradiation comprises a dose range of from 11-18 kGy.

Assignees

• Bookbinder Dana Craig
• Martin Arthur Winston
• Pal Santona
• Shogbon Christopher Bankole
• Weber Jennifer L
• Zhou Yue
• Corning Inc

Inventors

• Bookbinder Dana Craig
• Martin Arthur Winston
• Pal Santona
• Shogbon Christopher Bankole
• Weber Jennifer L
• Zhou Yue

Classifications

• C12N5/0068 Primary

  General culture methods using substrates (for specific animal cell type C12N5/06) · CPC title

• C12N2533/50

  Proteins · CPC title

• C12N2533/20

  Small organic molecules · CPC title