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US4176009A Expired / Lapsed US ⏱️ 0.0 years remaining

Method of measuring collagenase activity

Assignee: Ajinomoto Co Inc
•
Filing: 1977-11-21
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Granted: 1979-11-27
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Expires: 1997-11-21
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Abstract

Abstract A method of measuring collagenase activity using as substrates peptide derivatives having the structure A-Pro-B-Gly-C-Ala-Gly-E wherein A is a hydrophobic neutral or acidic chromophore, B is an amino acid residue, C is Ile or Leu, E is Gln-D-Arg-OH or D-Arg-OH and all the amino acid residues except for Gly are L-configuration unless otherwise stated.

Inventors

  • 👤 Shumpei Sakakibara
  • 👤 Yutaka Nagai
  • 👤 Kenji Fujiwara
  • 👤 Takahiro Sakai

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-07 09:57
CPC Classifications
C; C07; C07K; C07K5/00; C07K5/04; C07K5/08; C07K5/0802; C07K5/0804; C07K5/0808; C07K14/00; C07K14/435; C07K14/78; Y; Y10; Y10S; Y10S930/00; Y10S930/01; Y10S930/28

Claims Analysis

Total Claims: 10
Claim 1
Independent Claim 120 words
A method of measuring collagenase activity which comprises contacting a compound having the structure A-Pro-B-Gly-C-Ala-Gly-E with collagenase in an aqueous medium whereby said compound is hydrolyzed to release peptide fragments, extracting the released peptide fragments containing A with an organic solvent, and assaying the extract by subjecting the extract to colorimetry, said A being a hydrophobic, and neutral or acidic chromophore selected from the group consisting of 2,4-dinitrophenyl, 5-dimethyl-amino-1-naphthalene-sulfonyl, p-phenylazobenzyloxycarbonyl, p-nitrobenzyloxycarbonyl, p-(4-hydroxy-1-naphthylazo)-benzenesulfonyl and p-phenylazobenzoyl, said B being an amino acid residue of an alpha-amino acid having up to 15 carbon atoms occurring in protein, said C being Ile or Leu, said E being Gln-D-Arg-OH or D-Arg-OH, and all the amino acid residues except for Gly being L-configuration unless otherwise stated.
Claim 2
Independent Claim 120 words
A method of measuring collagenase activity which comprises contacting a compound having the structure A-Pro-B-Gly-C-Ala-Gly-E with collagenase in an aqueous medium whereby said compound is hydrolyzed to release peptide fragments, extracting the released peptide fragments containing A with an organic solvent, and assaying the extract by subjecting the extract to colorimetry, said A being a hydrophobic, and neutral or acidic chromophore selected from the group consisting of 2,4-dinitrophenyl, 5-dimethyl-amino-1-naphthalene-sulfonyl, p-phenylazobenzyloxycarbonyl, p-nitrobenzyloxycarbonyl, p-(4-hydroxy-1-naphthylazo)-benzenesulfonyl and p-phenylazobenzoyl, said B being an amino acid residue of an alpha-amino acid having up to 15 carbon atoms occurring in protein, said C being Ile or Leu, said E being Gln-D-Arg-OH or D-Arg-OH, and all the amino acid residues except for Gly being L-configuration unless otherwise stated.
Claim 3
Dependent Claim 30 words
A method as set forth in claim 1, wherein said contacting is carried out at a temperature of 30° to 45° C. and at a pH of 6 to 9.
Claim 4
Dependent Claim 40 words
A method as set forth in claim 2, wherein said A is 2,4-dinitrophenyl, said B is a residue of a compound selected from the group consisting of alanine, leucine and glutamine, said C is Ile and said E is Gln-D-Arg-OH.
Claim 5
Dependent Claim 32 words
A method as set forth in claim 1 wherein said collagenase activity is calculated by subtracting from the absorbance obtained by said colorimetry the absorbance obtained by substituting said compound by A-B-Gly-C-Ala-Gly-E.
Claim 6
Dependent Claim 27 words
A method as set forth in claim 4, wherein said A is 2,4-dinitrophenyl, said B is Gln or Ala, said C is Ile and E is Gln-D-Arg-OH.
Claim 7
Dependent Claim 32 words
A method as set forth in claim 2, wherein said collagenase activity is calculated by subtracting from the absorbance obtained by said colorimetry the absorbance obtained by substituting said compound by A-B-Gly-C-Ala-Gly-E.
Claim 8
Dependent Claim 23 words
A method as set forth in claim 2, wherein A is a compound selected from the group consisting of 2,4-dinitrophenyl, p-(4-hydroxy-1-napthylazo)-benzenesulfonyl and p-phenylazobenzoyl.
Claim 9
Dependent Claim 41 words
A method as set forth in claim 1, wherein B is a residue of a compound selected from the group consisting of glycine, alanine, valine, leucine, serine, threonine, proline, phenylalanine, tyrosine, tryptophane, lysine, arginine, aspartic acid, asparagine, glutamic acid and glutamine.
Claim 10
Dependent Claim 27 words
A method as set forth in claim 1, wherein B is a residue of a compound selected from the group consisting of alanine, proline, leucine and glutamine.

References Cited (Backward Citations)

US4016042A Cited
US4028318A Cited
US4070245A Cited
US4119620A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1982-11-26 1983-05-28 1983-11-27 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1986-11-26 1987-05-28 1987-11-27 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1990-11-26 1991-05-28 1991-11-27 $7700.00 Window Closed / Lapsed

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