US2012202713A1PendingUtilityA1

Constructs and libraries comprising antibody surrogate light chain sequences

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Assignee: BHATT RAMESHPriority: Mar 27, 2007Filed: Feb 10, 2012Published: Aug 9, 2012
Est. expiryMar 27, 2027(~0.7 yrs left)· nominal 20-yr term from priority
C07K 16/108C07K 2319/00C07K 16/241C40B 40/10C07K 16/08C07K 2317/622C07K 2317/34C07K 16/22C07K 16/28C07K 19/00C07K 16/00C07K 2317/56C07K 2317/52C07K 16/18C07K 16/005
56
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Claims

Abstract

The invention concerns constructs and libraries comprising antibody surrogate light chain sequences. In particular, the invention concerns constructs comprising VpreB sequences, optionally partnered with another polypeptide, such as, for example, antibody heavy chain variable domain sequences, and libraries containing the same.

Claims

exact text as granted — not AI-modified
1 - 88 . (canceled) 
     
     
         89 . A trimeric polypeptide complex comprising
 (a) a VpreB sequence; a λ5 sequence or an antibody light chain constant region sequence; and an antibody heavy chain sequence, or   (b) a λ5 sequence; an antibody light chain variable region sequence; and an antibody heavy chain sequence,   wherein said sequences are non-covalently associated with each other; and   wherein said trimeric polypeptide complex binds to a target.   
     
     
         90 . The complex of  claim 89 , comprising a VpreB1 sequence. 
     
     
         91 . The complex of  claim 90 , comprising all or part of a VpreB1 sequence of SEQ ID NO: 1. 
     
     
         92 . The complex of  claim 89 , comprising all or part of a λ5 sequence of SEQ ID NO: 6. 
     
     
         93 . The complex of  claim 91 , comprising all or part of a λ5 sequence of SEQ ID NO: 6. 
     
     
         94 . The complex of  claim 91 , wherein at least part of the C-terminal tail of said VpreB1 sequence is removed. 
     
     
         95 . The complex of  claim 93 , wherein at least part of the N-terminal tail of said λ5 sequence is removed. 
     
     
         96 . The complex of  claim 93 , wherein at least part of the C-terminal tail of said VpreB1 sequence and at least part of the N-terminal tail of said λ5 sequence is removed. 
     
     
         97 . The complex of  claim 94 , wherein the entire C-terminal tail of said VpreB1 sequence is removed. 
     
     
         98 . The complex of  claim 95 , wherein the entire N-terminal tail of said λ5 sequence is removed. 
     
     
         99 . The complex of  claim 98 , comprising at least part of the C-terminal tail of said VpreB1 sequence. 
     
     
         100 . The complex of  claim 99 , comprising the entire C-terminal tail of said VpreB1 sequence. 
     
     
         101 . The complex of  claim 96 , wherein the entire C-terminal tail of said VpreB1 sequence and the entire N-terminal tail of said λ5 sequence is removed. 
     
     
         102 . The complex of  claim 89  comprising a full-length VpreB1 sequence of SEQ ID NO: 1, and a λ5 sequence of SEQ ID NO: 6 having at least part of its N-terminal tail removed. 
     
     
         103 . The complex of  claim 102  comprising a full-length VpreB1 sequence of SEQ ID NO: 1, and a λ5 sequence of SEQ ID NO: 6 having its N-terminal tail removed. 
     
     
         104 . The complex of  claim 89  comprising a full-length λ5 sequence of SEQ ID NO: 6, and a VpreB1 sequence of SEQ ID NO: 1 having at least part of its C-terminal tail removed. 
     
     
         105 . The complex of  claim 104  comprising a full-length λ5 sequence of SEQ ID NO: 6, and a VpreB1 sequence of SEQ ID NO: 1 having its C-terminal tail removed. 
     
     
         106 . The complex of  claim 89  comprising a full-length VpreB1 sequence of SEQ ID NO: 1 and a full-length λ5 sequence of SEQ ID NO: 6. 
     
     
         107 . The complex of  claim 89 , comprising at least one additional functionality appended or substituted to a free end of the λ5 sequence and/or a free end of the VpreB sequence. 
     
     
         108 . The complex of  claim 98 , comprising at least one additional functionality appended or substituted to a free end of the λ5 sequence and/or a free end of the VpreB1 sequence. 
     
     
         109 . The complex of  claim 89 , wherein the complex comprises (a) a VpreB sequence, an antibody light chain constant region, and an antibody heavy chain sequence. 
     
     
         110 . A library comprising a complex of any one of  claims 89 . 
     
     
         111 . A library comprising the complex of  claim 107 . 
     
     
         112 . The library of  claim 111  comprising a random peptide library appended or substituted to said N-terminal or C-terminal tail present and panned for specific binding to a further target. 
     
     
         113 . The library of  claim 111  comprising an antibody or antibody fragment appended or substituted to said N-terminal or C-terminal tail present. 
     
     
         114 . The library of  claim 113  wherein said antibody or antibody fragment binds to the same target as said complex. 
     
     
         115 . The library of  claim 113  wherein said antibody or antibody fragment binds to a target different from the target to which said complex binds. 
     
     
         116 . The library of  claim 114  wherein said antibody or antibody fragment binds to a tumor antigen. 
     
     
         117 . The library of  claim 115  wherein said antibody or antibody fragment binds to a tumor antigen. 
     
     
         118 . The library of  claim 111  comprising a therapeutic peptide or therapeutic protein appended or substituted to said N-terminal or C-terminal tail present.

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