Mechanically interlocking complexes

Patent metadata

Field	Value
Publication number	US-11897952-B2
Application number	US-201615563093-A
Country	US
Kind code	B2
Filing date	Mar 30, 2016
Priority date	Mar 30, 2015
Publication date	Feb 13, 2024
Grant date	Feb 13, 2024

Abstract

Provided herein are functionalized monoclonal antibodies (mAbs) including antibody fragments, including those where a Fab-binding molecule (Fab binding moiety) linked to a steric hindering molecule (steric hindering chemical moiety) is mechanically interlocked (e.g., through noncovalent conjugation) with the antibody or antibody fragment. Also provided are compositions that form highly stable and versatile drug delivery and diagnostic compositions.

First claim

What is claimed is:

1. A mechanically interlocked complex comprising a compound mechanically interlocked with a fragment antigen-binding (Fab) domain,
said Fab domain comprising a hole within a central cavity lined by amino acid residues of the VH, VL, CH1, and CL regions of said Fab domain, wherein said central cavity comprises a non-CDR binding site;
wherein said amino acid residues of the VL region are a threonine at position 40, an asparagine at position 41, and an aspartate at position 85, according to Kabat numbering, and
wherein said amino acid residues of the VH region are a seine or proline at position 40 and an isoleucine, tyrosine, methionine, phenylalanine, or a tryptophan at position 89, according to Kabat numbering;
said compound comprising a Fab binding moiety attached to a steric hindering chemical moiety through a chemical linker,
wherein said Fab binding moiety is bound to said non-CDR binding site, said chemical linker passes through said hole, and steric hindrance occurs between said steric hindering chemical moiety and amino acids lining said hole thereby mechanically interlocking said compound and said Fab;
wherein said compound has the formula:
R 1 -L 1 -R 2

wherein R 1 is
R 3 —X0-X1-X2-X3-X4-X5-X6-X7-X8-X9-X10-X11-X12-R 4
wherein:
X0 is Ser or null;
X1 is Cys, Ser, Gly, β-alanine, diaminopropionic acid, β-azidoalanine, or null;
X2 is Gln or null;
X3 is Phe, Tyr, β,β′-diphenyl-Ala, His, Asp, 2-bromo-L-phenylalanine, 3-bromo-L-phenylalanine, 4-bromo-L-phenylalanine, Asn, Gln, a modified Phe, or a boronic acid-containing residue;
X4 is Asp or Asn;
X5 is Leu, β,β′-diphenyl-Ala, Phe, Trp, Tyr, tryptophan, or tyrosine, or a boronic acid-containing residue;
X6 is Ser or Cys;
X7 is Thr, Ser or Cys;
X8 is an amino acid comprising a side chain of the formula -L 1A -L 1 -R 2 ,
wherein L 1A is substituted or unsubstituted alkylene, substituted or unsubstituted heteroalkylene, substituted or unsubstituted cycloalkylene, substituted or unsubstituted heterocycloalkylene, substituted or unsubstituted arylene or substituted or unsubstituted heteroarylene;
wherein L 1 is said chemical linker of about 5 Å to about 15 Å in length; and
R 2 is said steric hindering chemical moiety wherein the longest bond length distance is at least 10 Å;
X9 is Arg or Ala;
X10 is Leu, Gln, Glu, β,β′-diphenyl-Ala, Phe, Trp, Tyr, tryptophan, or tyrosine, or a boronic acid-containing residue;
X11 is Lys or Arg;
X12 is Cys, Gly, 7-aminoheptanoic acid, β-alanine, diaminopropionic acid, propargylglycine, isoaspartic acid, or null,
R 3 and R 4 are independently null, -L 2 -R 5 or an amino acid peptide sequence optionally substituted with -L 2 -R 5 , wherein L 2 is a covalent or non-covalent linker and R 5 is a therapeutic agent, a diagnostic agent, or a detectable agent; and
wherein X1 and X12 are optionally joined together to form a cyclic peptidyl moiety.

2. The mechanically interlocked complex of claim 1 , wherein said non-CDR binding site is a peptide binding site comprising framework region amino acid residues and said Fab binding moiety is a peptidyl moiety.

3. The mechanically interlocked complex of claim 2 , wherein said peptidyl moiety binds to said peptide binding site with a K D of less than 10 nM.

4. The mechanically interlocked complex of claim 2 , wherein said peptidyl moiety binds to said peptide binding site with a K D of less than 1 nM.

5. The mechanically interlocked complex of claim 2 , wherein said peptidyl moiety binds to said peptide binding site with a τ 1/2 of more than 2000 seconds.

6. The mechanically interlocked complex of claim 1 , wherein said compound and said Fab are bound together with a τ 1/2 of more than 4500 seconds.

7. The mechanically interlocked complex of claim 1 , wherein said chemical linker is a substituted or unsubstituted alkylene, substituted or unsubstituted heteroalkylene, substituted or unsubstituted cycloalkylene, substituted or unsubstituted heterocycloalkylene, substituted or unsubstituted arylene or substituted or unsubstituted heteroarylene.

8. The mechanically interlocked complex of claim 1 , wherein L 1A is —(CH 2 ) 3 —NH(N)—NH—.

9. The mechanically interlocked complex of claim 1 , wherein R 3 and R 4 are independently null, -L 2 -R 5 or a 1 to 100 amino acid peptide sequence optionally substituted with -L 2 -R 5 , wherein L 2 is a covalent or non-covalent linker and R 5 is a therapeutic agent, a diagnostic agent, or a detectable agent.

10. The mechanically interlocked complex of claim 1 , wherein R 3 is a three amino acid peptide sequence optionally substituted with -L 2 -R 5 .

11. The mechanically interlocked complex of claim 1 , wherein the non-CDR binding site is formed by amino acids at positions 8, 9, 10, 38, 39, 40, 41 42, 43, 44, 45, 82, 83, 84, 85, 86, 87, 99, 100, 101, 102, 103, 104, 105, 142, 162, 163, 164, 165, 166, 167, 168, and 173 of the light chain and 6, 9, 38, 39, 40, 41, 42, 43, 44, 45, 84, 86, 87, 88, 89, 90, 91, 103, 104, 105, 106, 107, 108, 111, 110, 147, 150, 151, 152, 173, 174, 175, 176, 177, 185, 186, and 187 of the heavy chain of the Fab, according to Kabat numbering.

12. A method of binding an antigen, said method comprising contacting an antigen with said mechanically interlocked complex of claim 1 and allowing said Fab to bind said antigen.

Assignees

• Hope City

Inventors

• Williams John
• Bzymek Krzysztof P
• Horne David
• Xie Jun

Classifications

• C07K16/02 Primary

  from eggs · CPC title

• C07K7/06

  having 5 to 11 amino acids · CPC title

• C07K7/08

  having 12 to 20 amino acids (gastrins C07K14/595; somatostatins C07K14/655; melanotropins C07K14/68) · CPC title

• C07K14/7051

  T-cell receptor (TcR)-CD3 complex · CPC title

• C07K16/2869 Primary

  against hormone receptors (for antibodies against neuromediator receptors C07K16/286) · CPC title