US2017247432A1PendingUtilityA1
Display of binding agents
Assignee: F-STAR BIOTECHNOLOGISCHE FORSCHUNGS- UND ENTW M B HPriority: Jun 26, 2007Filed: May 16, 2017Published: Aug 31, 2017
Est. expiryJun 26, 2027(~0.9 yrs left)· nominal 20-yr term from priority
C07K 2317/569C07K 16/005G01N 33/6857C07K 2318/10C07K 2317/52C40B 30/04C07K 16/32G01N 2333/70535
56
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Claims
Abstract
The present application relates to a method of preparing a genetic package displaying oligomers of modular antibody domains binding to a target and to a scaffold ligand as well as to vectors and libraries of genetic packages produced thereby. The invention further relates to methods of selecting suitable linker sequences for use in such oligomer display.
Claims
exact text as granted — not AI-modifiedWe claim:
1 . A method of producing a functional binding agent, wherein the functional binding agent binds to a target antigen, wherein said target antigen is a receptor of the erbB class, wherein the functional binding agent is an antibody Fc fragment comprising a CH2 domain and a CH3 domain, comprising the steps of:
a. providing a library of said antibody Fc fragments, b. contacting said library with said target antigen in the presence of a scaffold ligand, wherein said target antigen and said scaffold ligand are different molecules, wherein said scaffold ligand is selected from the group consisting of CD64, CD16, CD32, FcRn and Protein A, c. selecting a library member binding to said target antigen in the presence of said scaffold ligand to obtain a functional binding agent, and d. producing a preparation of the functional binding agent.
2 . The method of claim 1 , wherein said library contains at least 10 2 independent clones expressing functional binding agents.
3 . The method of claim 1 , wherein said library contains at least 10 6 independent clones expressing functional binding agents.
4 . The method of claim 1 , wherein said target antigen is human Her2.
5 . The method of claim 1 , wherein the functional binding agent has a molecular weight of less than 60 kD.
6 . The method of claim 1 , wherein the functional binding agent has a target binding affinity of Kd<10 −8 M.
7 . The method of claim 1 , further comprising the steps of:
e) affinity maturating the functional binding agent by amino acid variation to obtain an affinity matured pool of binding agents, and f) selecting a member of said pool which binds to the target antigen in the presence of the scaffold ligand to obtain an affinity maturated functional binding agent.
8 . The method of claim 7 , wherein the affinity maturated functional binding agent exhibits at least a 10 fold increase in affinity of binding to the target antigen compared to the functional binding agent.Join the waitlist — get patent alerts
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