US2021355180A1PendingUtilityA1

Alzheimer abeta peptide binding polypeptide

Assignee: AMYLONIX ABPriority: Feb 20, 2015Filed: Jul 22, 2021Published: Nov 18, 2021
Est. expiryFeb 20, 2035(~8.6 yrs left)· nominal 20-yr term from priority
A61P 21/00A61K 38/00A61P 27/06A61P 27/12C07K 14/4711C07K 2317/92A61P 43/00A61P 25/16A61P 25/28A61P 3/10A61P 27/02A61P 25/00
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Claims

Abstract

The present disclosure relates to a class of engineered polypeptides having a binding affinity for amyloid β (Aβ) peptides (in the following referred to as Aβ), comprising the amino acid sequence EX2X3YX5X6NLX9A X11QLCAX16IX18X19X20 ED (SEQ ID NO:632). The present disclosure also relates to the use of such Aβ peptide binding polypeptides as therapeutic, prognostic and/or diagnostic agents.

Claims

exact text as granted — not AI-modified
1 . An Aβ peptide binding polypeptide which comprises
 a first moiety comprising a first Aβ peptide binding motif BM1, 
 a second moiety comprising a second Aβ peptide binding motif BM2), and 
 a linker, 
 wherein each one of said binding motifs BM1 and BM2 consists of the amino acid sequence selected from 
 
       
         
           
                 
                 
               
                     
                   i) 
                 
                     
                   (SEQ ID NO: 632) 
                 
                     
                   EX 2 X 3 YX 5 X 6 NLX 9 A X 11 QLCAX 16 IX 18 X 19 X 20  ED 
                 
             
                
                
                
               
            
           
         
         wherein, independently from each other,
 X 2  is selected from I, M, Q, R, T and Y; 
 X 3  is selected from H and V; 
 X 5  is selected from F, I and L; 
 X 6  is selected from P and T; 
 X 9  is selected from N and T; 
 X 11  is selected from D and H; 
 X 16  is selected from F and I; 
 X 18  is selected from N, Q and R; 
 X 19  is selected from K and 5; and 
 X 20  is selected from F, I, L and R; 
 
         and 
         ii) an amino acid sequence which has at least 95% identity to the full-length sequence defined in i). and 
         wherein the amino acid sequence of the BM1 and the amino acid sequence of the BM2 are the same or different 
       
     
     
         2 . The Aβ peptide binding polypeptide according to  claim 1 , wherein at least one of the first and second moieties comprises a binding module amino acid sequence, Bmod, selected from 
       
         
           
                 
                 
               
                     
                   iii) 
                 
                     
                   (SEQ ID NO: 562) 
                 
                     
                   [BM]-DXaSQXbXcXdLLXe EAKKLXfXgXhQA PXi 
                 
             
                
                
                
               
            
           
         
         wherein BM is the BM1 or the BM2 as defined in  claim 1 , and, independently of each other,
 Xa is selected from P, Q, R and 5; 
 Xb is selected from N, Q, R and 5; 
 Xc is selected from A and 5; 
 Xd is selected from K, N and E; 
 Xe is selected from A, S and C; 
 Xf is selected from E, N and 5; 
 Xg is selected from D, E and 5; 
 Xh is selected from A and 5; and 
 Xi is selected from no amino acid, A and K, 
 
         and 
         iv) an amino acid sequence which has at least 97% identity to the full-length sequence defined in iii). 
       
     
     
         3 . The Aβ peptide binding polypeptide according to  claim 2 , wherein sequence iii) consists of the amino acid sequence 
       
         
           
                 
                 
               
                     
                   (SEQ ID NO: 563) 
                 
                     
                   [BM]-DXaSQXbAXdLLA EAKKLNDAQA PXi 
                 
             
                
                
               
            
           
         
         wherein BM is the BM1 or the BM2, and, independently of each other,
 Xa is selected from P, Q, R and 5; 
 Xb is selected from N, Q, R and 5; 
 Xd is selected from K and N; and 
 Xi is selected from no amino acid, A and K. 
 
       
     
     
         4 . The Aβ peptide binding polypeptide according to  claim 1 , wherein
 sequence i) of the BM1 is amino acid residues 4-25 in any one of SEQ ID NO:1-106 and 118-553, and 
 sequence i) of the BM2 is amino acid residues 64-85 in any one of SEQ ID NO:1-17, 19-106 and 118-553 or amino acid residues 69-90 in SEQ ID NO:18. 
 
     
     
         5 . The Aβ peptide binding polypeptide according to  claim 4 , wherein
 sequence i) of the BM1 is amino acid residues 4-25 in SEQ ID NO:95 and 
 sequence i) of the BM2 is amino acid residues 64-85 in SEQ ID NO:95. 
 
     
     
         6 . The Aβ peptide binding polypeptide according to  claim 2 , wherein
 sequence iii) of the Bmod of the first moiety is amino acid residues 4-47 in any one of SEQ ID NO:1-106 and 118-553, and 
 sequence iii) of the Bmod of the second moiety is amino acid residues 64-107 in any one of SEQ ID NO:1-17, 19-106 and 118-553 or amino acid residues 69-112 in SEQ ID NO:18. 
 
     
     
         7 . The Aβ peptide binding polypeptide according to  claim 6 , wherein
 sequence iii) of the Bmod of the first moiety is amino acid residues 4-47 in SEQ ID NO:95, and 
 sequence iii) of the Bmod of the second moiety is amino acid residues 64-107 in SEQ ID NO:95. 
 
     
     
         8 . An Aβ peptide binding polypeptide comprising an amino acid sequence selected from the group consisting of SEQ ID NO:1-106 and 118-553. 
     
     
         9 . The Aβ peptide binding polypeptide according to  claim 1 , which is capable of binding to Aβ peptide such that the K D  value of the interaction is at most 1×10 −7  M. 
     
     
         10 . A fusion protein or conjugate, comprising
 a first part consisting of the Aβ peptide binding polypeptide according to  claim 1 ; and   a second part consisting of a polypeptide having a biological activity.   
     
     
         11 . The fusion protein or conjugate according to  claim 10 , wherein said biological activity is a binding activity. 
     
     
         12 . The fusion protein or conjugate according to  claim 10 , wherein the second part is selected from the group consisting of antibodies and antigen binding fragments thereof. 
     
     
         13 . A composition comprising the Aβ peptide binding polypeptide according to  claim 1  and at least one pharmaceutically acceptable excipient or carrier. 
     
     
         14 . The Aβ binding polypeptide of  claim 8 , comprising an amino acid sequence selected from the group consisting of SEQ ID NO:1, 5, 9, 13, 14, 16, 18, 20, 21, 25, 26, 28, 33, 35, 37, 40, 42, 48, 49, 50, 51, 53, 54, 55, 59, 60, 61, 62, 64, 65, 70, 72, 75, 78, 84, 89, 90, 95, 96, 97, 100, 104 and 118-159. 
     
     
         15 . The Aβ binding polypeptide of  claim 8 , comprising an amino acid sequence selected from the group consisting of SEQ ID NO:18, 28, 35, 49, 50, 51, 55, 59, 64, 65, 70, 72, 78, 84, 95 and 118-159. 
     
     
         16 . The Aβ binding polypeptide of  claim 8 , comprising an amino acid sequence selected from the group consisting of SEQ ID NO 18, 70 and 95. 
     
     
         17 . The Aβ binding polypeptide of  claim 8 , comprising an amino acid sequence consisting of SEQ ID NO:95. 
     
     
         18 . The fusion protein or conjugate according to  claim 11 , wherein said binding activity is binding to a target selected from the group consisting of Tau, apolipoprotein E (ApoE), beta-secretase 1 (BACE1), gamma-secretase, transferrin receptor (TfR), complement factor Cis, presenilin 1, presenilin 2, nicastrin, alpha-synuclein and Bri. 
     
     
         19 . The composition of  claim 13 , further comprising at least one active agent, said active agent selected from the group consisting of inhibitors of neurotransmitter degradation, neurotransmitters, acetylcholinesterase inhibitors, NMDA receptor antagonists, TNF inhibitors, antihistamines, anti-viral agents, alpha-secretase activators, inhibitors of beta- or gamma-secretase, inhibitors of α-synuclein aggregation, inhibitors of tau aggregation, calcium channel blockers, compounds effective against oxidative stress, anti-apoptotic compounds, metal chelators, pirenzepin and metabolites, attractants for Aβ clearing/depleting cellular components, inhibitors of N-terminal truncated Aβ including pyroglutamated Aβ3-42, anti-inflammatory molecules, clozapine, ziprasidone, risperidone, aripiprazole, olanzapine, tacrine, rivastigmine, donepezil, galantamine, amyloid or tau modifying drugs, vitamin B12, cysteine, acetylcholine precursor, lecithin, choline,  Ginkgo biloba , acetyl-L-carnitine, idebenone, propentofylline, xanthine derivatives, and combinations thereof. 
     
     
         20 . A method for the treatment of an Aβ peptide associated condition, comprising administering to a subject in need thereof, an effective amount of the Aβ peptide binding polypeptide according to  claim 1 .

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