IP Library Granted Patent US 7,968,683
Granted Patent B1
US 7,968,683 · App. 12/437,116 · Granted Jun 28, 2011

Factor IXa crystals, related complexes and methods

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Quick Facts
Patent No.
US 7,968,683
App. No.
12/437,116
Granted
Jun 28, 2011
Kind
B1
Abstract

The present invention relates to factor IXa complexes and crystals thereof as well as methods for identifying inhibitors of factor IXa.

Claims (28)

1. A crystalline complex comprising Factor IXa bound to a peptide and a compound, wherein said Factor IXa comprises a polypeptide selected from the group consisting of SEQ ID NO: 14 or SEQ ID NO: 18, said peptide comprises SEQ ID NO: 13 and said compound is selected from the group consisting of:

wherein said crystal complexes form in the following crystalline forms:

(i) when said complex is formed with compound (a) said crystal forms in space group P2 1 2 1 2 1 having unit cell dimensions a=48.1 Å, b=69.8 Å, c=92.1 Å and α=β=γ=90° or space group P4 3 2 1 2 having unit cell dimensions a=100.4 Å, b=100.4 Å, c=97.3 Å and α=β=γ=90°;

(ii) when said complex is formed with compound (b) said crystal forms in space group P4 3 2 1 2 having unit cell dimensions a=100.6 Å, b=100.6 Å, c=98.1 Å and α=β=γ=90°;

(iii) when said complex is formed with compound (c) said crystal forms in space group P4 3 2 1 2 having unit cell dimensions a=99.2 Å, b=99.2 Å, c=97.3 Å and α=β=γ=90°; and

(iv) when said complex is formed with compound (d) said crystal forms in space group P4 3 2 1 2 having unit cell dimensions a=100.5 Å, b=100.5 Å, c=98.4 Å and α=β=γ=90°.

2. The crystalline complex of claim 1 in an aqueous composition.

3. The crystalline complex of claim 1 wherein said composition comprises a precipitant.

4. The crystalline complex of claim 1 wherein the complex is characterized by structural coordinates comprising a root mean square deviation of conserved residue backbone atoms or of alpha carbon atoms of less than about 1.5 Å when superimposed on backbone atoms described in Table 2 or 4.

5. The crystalline complex of claim 1 wherein the complex is characterized by structural coordinates comprising a root mean square deviation of conserved residue backbone atoms or of alpha carbon atoms of less than about 1.5 Å when 5 superimposed on backbone atoms described in Table 3.

6. The crystalline complex of claim 1 wherein the complex is characterized by structural coordinates comprising a root mean square deviation of conserved residue backbone atoms or of alpha carbon atoms of less than about 1.5 Å when 10 superimposed on backbone atoms described in Table 5.

7. The crystalline complex of claim 1 wherein the complex is characterized by structural coordinates comprising a root mean square deviation of conserved residue backbone atoms or of alpha carbon atoms of less than about 1.5 Å when 15 superimposed on backbone atoms described in Table 6.

8. The crystalline complex of claim 1 (i) which can diffract X-rays for structural determination of said complex to a resolution of about 1.64 angstroms or 3.0 angstroms, respectively, or better.

9. The crystalline complex of claim 1 (ii) which can diffract X-rays for structural determination of said complex to a resolution of about 2.45 angstroms or better.

10. The crystalline complex of claim 1 (iii) which can diffract X-rays for structural determination of said complex to a resolution of about 2.30 angstroms or better.

11. The crystalline complex of claim 1 (iv) which can diffract X-rays for structural determination of said complex to a resolution of about 2.50 angstroms or better.

12. A method for producing a crystal of factor IXa complexed with a compound represented by structural formula A:

comprising mixing about 0.5 μl of a solution comprising about 6 mg/ml of the factor IXa-compound A complex in 25 mM Tris, pH 8.0 and 0.15 M sodium chloride with about 0.5 μl of precipitant solution comprising about 20% PEG-6000 (v/v), 0.1 M citric acid, pH 5.9 and incubating the mixture in the presence of about 0.08 mL of the precipitant solution, at about 4° C., in a sealed container, wherein said Factor IXa comprises SEQ ID NO: 14 or SEQ ID NO: 18 bound to SEQ ID NO: 13.

13. A method for producing a crystal of factor IXa complexed with a compound represented by structural formula B:

comprising mixing about 0.5 μl of a solution comprising about 15 mg/ml of the factor IXa-compound B complex in 25 mM Tris, pH 8.0, 0.15 M sodium chloride, with about 0.5 μl of a precipitant solution comprising 16% PEG-6000 (v/v), 0.1 M citric acid, pH 5.9 and incubating the mixture in the presence of about 0.08 mL of the precipitant solution, at about 4° C., in a sealed container, wherein said Factor IXa comprises SEQ ID NO: 14 or SEQ ID NO: 18 bound to SEQ ID NO: 13.

14. A method for producing a crystal of factor IXa complexed with a compound represented by structural formula A

comprising incubating the crystal of claim 1 (b)(ii) in a drop comprising about 1 mM of the compound represented by structural formula A, 1% DMSO, 16% PEG 6000 (v/v), 0.1 M citric acid, pH 5.9, in an aqueous solution, at about 4° C.

15. A method for producing a crystal of factor IXa complexed with a compound

represented by structural formula C:

comprising mixing about 0.5 μl of a solution comprising about 10 mg/ml of the factor IXa-formula C complex in 25 mM Tris, pH 8.0, 0.15 M sodium chloride, 1% DMSO buffer with about 0.5 μl of precipitant solution comprising 14% PEG 6000 (v/v), 0.1 M citric acid, pH 5.67 and incubating the mixture in the presence of about 0.08 mL of the precipitant solution at about 4° C. in a sealed container, wherein said Factor IXa comprises SEQ ID NO: 14 or SEQ ID NO: 18 bound to SEQ ID NO: 13.

16. A method for producing a crystal of factor IXa complexed with a compound represented by structural formula D:

comprising incubating the crystal of claim 1 (d)(iv) in a drop comprising about 1 mM of said compound represented by structural formula D, 1% DMSO, 14% PEG 6000 (v/v),

0.1 M citric acid, pH 5.67 in an aqueous solution at about 4° C., wherein said Factor IXa comprises SEQ ID NO: 14 or SEQ ID NO: 18 bound to SEQ ID NO: 13.

Assignments (1)
CHANGE OF NAME Recorded Aug 30, 2012
From: SCHERING CORPORATION
To: MERCK SHARP & DOHME CORP.
Reel/Frame 028884/0151 →