Human neutrophil gelatinase-associated lipocalin (hNGAL) muteins capable of binding angiopoietin-2 (Ang-2) and methods of use thereof

Patent metadata

Field	Value
Publication number	US-10526382-B2
Application number	US-201615546609-A
Country	US
Kind code	B2
Filing date	Jan 27, 2016
Priority date	Jan 28, 2015
Publication date	Jan 7, 2020
Grant date	Jan 7, 2020

Abstract

The present disclosure provides hNGAL muteins that bind Ang-2 and can be used in various application including pharmaceutical applications, for example, to inhibit or reduce angiogenesis. The present disclosure also concerns methods of making one or more muteins described herein as well as compositions and combinations comprising one or more of such muteins. The present disclosure further relates to nucleic acid molecules encoding such muteins and to methods for generation of such muteins and nucleic acid molecules. In addition, the application discloses therapeutic and/or diagnostic uses of these muteins as well as compositions and combinations comprising one or more of such muteins.

First claim

The invention claimed is:

1. A human neutrophil gelatinase associated lipocalin (hNGAL) mutein that is capable of binding angiopoietin-2 (Ang-2) with detectable affinity,
wherein the mutein comprises the following mutated amino acid residue in comparison with the linear polypeptide sequence of mature hNGAL (SEQ ID NO: 16): Gln 28→His,
wherein the mutein comprises at least fifteen of the following mutated amino acid residues in comparison with the linear polypeptide sequence of mature hNGAL (SEQ ID NO: 16): Leu 36→Gln, Glu, His, Val, Met or Phe; Ala 40→Val, Tyr, His or Trp; Ile 41→His, Tyr, Trp, Val, Arg, Glu, or Asp; Gln 49→Gly, Ile, Glu or Val; Tyr 52→Trp, His, Thr or Ser; Ser 68→Gly, Asp, Gln, Glu or Ile; Leu 70→Ser, Thr, Gly, Arg, Tyr or Ala; Arg 72 Gly, Ala, Trp, Thr or Glu; Lys 73→Pro, Phe, Leu, Arg, Ala or Gln; Asp 77→Asn, Lys, Ser or Val; Trp 79→Thr, Arg, Ser or Asn; Arg 81→Trp, His or Tyr; Asn 96→Gly, Ala, Pro, Gln or Asp; Tyr 100→Pro, Trp, Gly, Ser, Leu or Asp; Leu 103→Gly, Glu, Asp, Met or Gln; Tyr 106→Thr, Leu, Phe, or Pro; Lys 125→His, Thr or Gly; Ser 127→Leu, Met, or Tyr; Tyr 132→Phe, Trp or Val; and Lys 134→Ala, Glu or Trp, and
wherein the mutein has a sequence identity of at least 85% to a sequence selected from the group consisting of SEQ ID NOs: 1-14.

2. The hNGAL mutein of claim 1 , wherein the mutein is capable of binding Ang-2 with a dissociation constant (KD) of about 5 nM or lower.

3. The hNGAL mutein of claim 1 , wherein the mutein is capable of binding Ang-2 with an affinity measured by an EC50 value of about 5 nM or lower.

4. The hNGAL mutein of claim 1 , wherein the mutein is capable of binding Ang-2 with an affinity measured by an IC50 value of about 5 nM or lower.

5. The hNGAL mutein of claim 1 , wherein the mutein is capable of inhibiting or reducing lymphatic microvascular endothelial cell proliferation mediated by Ang-2 with an IC50 value of about 5 nM or lower.

6. The hNGAL mutein of claim 1 , wherein the mutein comprises a mutated amino acid residue at sixteen or more positions corresponding to positions 36, 40, 41, 49, 52, 65, 68, 70, 72-74, 77, 79, 81, 87, 96, 100, 103, 106, 116, 125, 126, 127, 129, 132, and 134 of the linear polypeptide sequence of mature hNGAL (SEQ ID NO: 16).

7. The hNGAL mutein of claim 1 , wherein the mutein comprises one or more of the following mutated amino acid residues in comparison with the linear polypeptide sequence of mature hNGAL (SEQ ID NO: 16): Asn 65→Asp; Lys 74→Glu; Cys 87→Ser; Asn 116→Asp; Val 126→Met; and Asn 129→Asp.

8. The hNGAL mutein of claim 1 , wherein the mutein comprises one of the following sets of mutated amino acid residues in comparison with the linear polypeptide sequence of mature hNGAL (SEQ ID NO: 16):
(a) Gln 28→His; Leu 36→Gln; Ala 40→Tyr; Gln 49→Gly; Tyr 52→Trp; Ser 68→Gly; Leu 70→Ser; Arg 72→Gly; Lys 73→Pro; Asp 77→Asn; Trp 79→Thr; Arg 81→Trp; Cys 87→Ser; Asn 96→Gly; Tyr 100→Pro; Leu 103→Gly; Tyr 106→Thr; Lys 125→His; Ser 127→Leu; Tyr 132→Phe; Lys 134→Glu;
(b) Gln 28→His; Leu 36→Phe; Ala 40→His; Ile 41→Arg; Gln 49→Gly; Tyr 52→His; Ser 68→Asp; Leu 70→Thr; Arg 72→Ala; Lys 73→Phe; Asp 77→Asn; Trp 79→Arg; Arg 81→His; Cys 87→Ser; Tyr 100→Trp; Leu 103→Glu; Tyr 106→Thr; Lys 125→Thr; Ser 127→Met; Tyr 132→Trp; Lys 134→Trp;
(c) Gln 28→His; Leu 36→Val; Ala 40→Trp; Ile 41→Tyr; Gln 49→Ile; Tyr 52→Thr; Ser 68→Gln; Leu 70→Gly; Arg 72→Glu; Lys 73→Gln; Asp 77→Lys; Trp 79→Ser; Arg 81→His; Cys 87→Ser; Asn 96→Asp; Tyr 100→Trp; Leu 103→Asp; Tyr 106→Leu; Lys 125→Gly; Ser 127→Met; Tyr 132→Val; Lys 134→Ala;
(d) Gln 28→His; Leu 36→Glu, Ala 40→Val; Ile 41→Glu; Gln 49→Val; Tyr 52→Thr Ser 68→Glu; Leu 70→Arg; Arg 72→Trp; Lys 73→Leu; Asp 77→Lys; Trp 79→Asn; Arg 81→His; Cys 87→Ser; Asn 96→Ala; Tyr 100→Gly; Leu 103→Met; Tyr 106→Thr; Lys 125→Thr; Ser 127→Met; Tyr 132→Trp; Lys 134→Trp;
(e) Gln 28→His; Leu 36→Gln; Ala 40→Tyr; Ile 41→Trp; Gln 49→Ile; Tyr 52→Ser; Ser 68→Ile; Leu 70→Tyr; Arg 72→Thr; Lys 73→Arg; Asp 77→Ser; Trp 79→Arg; Arg 81→Tyr; Cys 87→Ser; Asn 96→Pro; Leu 103→Asp; Tyr 106→Thr; Lys 125→His; Ser 127→Tyr; Tyr 132→Trp; Lys 134→Glu;
(f) Gln 28→His; Leu 36→Gln; Ala 40→Tyr; Gln 49→Glu; Tyr 52→Trp; Asn 65→Asp; Ser 68→Gly; Leu 70→Ser; Arg 72→Gly; Lys 73→Pro; Asp 77→Asn; Trp 79→Arg; Arg 81→Trp; Cys 87→Ser; Asn 96→Gly; Tyr 100→Ser; Leu 103→Gln; Tyr 106→Thr; Lys 125→His; Ser 127→Leu; Tyr 132→Phe; Lys 134→Glu;
(g) Gln 28→His; Leu 36→His; Ala 40→Tyr; Gln 49→Glu; Tyr 52→Trp; Asn 65→Asp; Ser 68→Glu; Leu 70→Ser; Arg 72→Gly; Lys 73→Pro; Asp 77→Asn; Trp 79→Arg; Arg 81→Trp; Cys 87→Ser; Asn 96→Gly; Tyr 100→Pro; Leu 103→Asp; Tyr 106→Thr; Lys 125→His; Ser 127→Leu; Tyr 132→Phe; Lys 134→Glu;
(h) Gln 28→His; Leu 36→Gln; Ala 40→Tyr; Gln 49→Gly; Tyr 52 Trp; Asn 65→Asp; Ser 68→Glu; Leu 70→Ser; Arg 72→Gly; Lys 73→Ala; Asp 77→Asn; Trp 79→Arg; Arg 81→Trp; Cys 87→Ser; Asn 96→Gly; Tyr 100→Asp; Leu 103→Gly; Tyr 106→Thr; Lys 125→His; Ser 127→Leu; Tyr 132→Phe; Lys 134→Glu;
(i) Gln 28→His; Leu 36→His; Ala 40→Tyr; Gln 49→Gly; Tyr 52 Trp; Asn 65→Asp; Ser 68→Glu; Leu 70→Ser; Arg 72→Gly; Lys 73→Pro; Asp 77→Asn; Trp 79→Arg; Arg 81→Trp; Cys 87→Ser; Asn 96→Gly; Tyr 100→Pro; Leu 103→Gly; Tyr 106→Thr; Lys 125→His; Ser 127→Leu; Tyr 132→Phe; Lys 134→Glu;
(j) Gln 28→His; Leu 36→Gln; Ala 40→Tyr; Tyr 52 Trp; Asn 65→Asp; Ser 68→Gly; Leu 70→Ser; Arg 72→Gly; Lys 73→Ala; Asp 77→Val; Trp 79→Arg; Arg 81→Trp; Cys 87→Ser; Asn 96→Gly; Tyr 100→Pro; Leu 103→Gly; Tyr 106→Thr; Lys 125→His; Ser 127→Leu; Tyr 132→Phe; Lys 134→Glu;
(k) Gln 28→His; Leu 36→Gln; Ala 40→Tyr; Gln 49→Val; Tyr 52 Trp; Asn 65→Asp; Ser 68→Glu; Leu 70→Ser; Arg 72→Gly; Lys 73→Pro; Asp 77→Asn; Trp 79→Arg; Arg 81→Trp; Cys 87→Ser; Asn 96→Gly; Tyr 100→Leu; Leu 103→Gly; Tyr 106→Thr; Lys 125→His; Ser 127→Leu; Tyr 132→Phe; Lys 134→Glu;
(l) Gln 28→His; Leu 36→Val; Ala 40→Trp; Ile 41→Tyr; Gln 49→Ile; Tyr 52 Thr; Asn 65→Asp; Ser 68→Gln; Leu 70→Gly; Arg 72→Glu; Lys 73→Gln; Lys 74→Glu; Asp 77→Lys; Trp 79→Ser; Arg 81→His; Cys 87→Ser; Tyr 100→Trp; Leu 103→Asp; Tyr 106→Pro; Asn 116→Asp; Lys 125→Gly; Ser 127→Met; Asn 129→Asp; Tyr 132→Val; Lys 134→Ala;
(m) Gln 28→His; Leu 36→Val; Ala 40→Trp; Ile 41→Tyr; Gln 49→Ile; Tyr 52 Thr; Asn 65→Asp; Ser 68→Gln; Leu 70→Gly; Arg 72→Glu; Lys 73→Gln; Lys 74→Glu; Asp 77→Lys; Trp 79→Ser; Arg 81→His; Cys 87→Ser; Asn 96→Asp; Tyr 100→Trp; Leu 103→Asp; Tyr 106→Pro; Lys 125→Gly; Val 126→Met; Ser 127→Met; Asn 129→Asp; Tyr 132→Val; Lys 134→Ala; or
(n) Gln 28→His; Leu 36→Met; Ala 40→Trp; Ile 41→Asp; Gln 49→Ile; Tyr 52 Thr; Asn 65→Asp; Ser 68→Gln; Leu 70→Ala; Arg 72→Glu; Lys 73→Gln; Asp 77→Lys; Trp 79→Ser; Arg 81→His; Cys 87→Ser; Asn 96→Gln; Tyr 100→Trp; Leu 103→Asp; Tyr 106→Pro; Lys 125→Gly; Ser 127→Met; Tyr 132→Val; Lys 134→Ala.

9. The hNGAL mutein of claim 1 , wherein the mutein comprises an amino acid sequence selected from the group consisting of SEQ ID NOs: 1-14.

10. The hNGAL mutein of claim 1 , wherein the mutein has at least 90% identity to an amino acid sequence selected from the group consisting of SEQ ID NOs: 1-14.

11. The hNGAL mutein of claim 1 , wherein the mutein is capable of binding angiopoietin-1 (Ang-1) with detectable affinity.

12. The hNGAL mutein of claim 11 , wherein the mutein is capable of binding Ang-1 with an affinity measured by an IC50 value of about 150 nM or lower.

13. The hNGAL mutein of claim 11 , wherein the mutein comprises a mutated amino acid residue at sixteen or more positions corresponding to positions 36, 40, 41, 49, 52, 65, 68, 70, 72-74, 77, 79, 81, 87, 96, 100, 103, 106, 116, 125, 126, 127, 129, 132, and 134 of the linear polypeptide sequence of mature hNGAL (SEQ ID NO: 16).

14. The hNGAL mutein of claim 11 , wherein the mutein comprises an amino acid sequence selected from the group consisting of SEQ I

Assignees

• Pieris Pharmaceuticals Gmbh

Inventors

• Bel Aiba Rachida Siham
• Allersdorfer Andrea
• Wiedenmann Alexander
• Rothe Christine
• Olwill Shane
• Gille Hendrik
• Audoly Laurent

Classifications

• G01N33/6893

  related to diseases not provided for elsewhere · CPC title

• C07K14/515

  Angiogenesic factors; Angiogenin · CPC title

• C07K14/47 Primary

  from mammals · CPC title

• A61K38/1709

  from mammals · CPC title

• A61P43/00

  Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00 · CPC title