A second look at antibody humanization by CDR-Graft
Transcript of A second look at antibody humanization by CDR-Graft
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A second look at antibody humanization
by CDR-Graft Reasons why CDR grafts fail
Annemarie Honegger, EMBL-EBI Industry Programme Workshop: Antibody Informatics 10-11 July 2012!
Recent applications of bioinformatics to antibody engineering
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Specificity Affinity
Selectivity
Folding Stability
Immuno- genicity
J.Biol.Chem. 275, 2795-803 (2000)
CDR Grafts
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Antigen Contacts
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Upper core packing
Nterm, outer loop
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CDR-Donors: Rabbit Antibodies
• Germline sequence alignment retrieved from IMGT • ~1000 rabbit VH, ~500 Vκ and ~30 Vλ retrieved from NCBI • Less sequence variability than human and murine antibodies, • frameworks huVκ1 and huVH3-like • Several features found that are not seen in human and
murine variable domains • Only two rabbit antibody structures found in the pdb:
3NL4 (1.54Å res.) is annotated as such, 2X7L isn’t.
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Yet another numbering scheme for immunoglobulin variable domains: An automatic modeling and analysis tool J.Mol.Biol. 309 (2001) 657-670AAAAA http://www.bioc.uzh.ch/antibody
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CDR-Donors: Rabbit Antibodies Murine and human antibody repertoires are quite similar – the rabbit repertoire is different: Vκ-Domains • Rabbit kappa light chains contain an additional Cys in position L98 (L80),
which can form a disulfide bond with a Cys in CL
• Chothia canonical rules do not recognize most rabbit CDR L1s, although there is no reason why they should not assume the conformation appropriate to their length
• There is less length variability in CDR-L1 of rabbit Vκ domains than in human and murine kappa domainsCDR L3 in rabbit Vκ lack Gln L108 (L90) and cis-Pro L136 (L?), which in human and murine Vκ domains produce the typical Ω-loop conformation. This produces a lambda-like CDR-L3 which might increase the flexibility of the VL/VH interface.
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CDR-Donors: Rabbit Antibodies Murine and human antibody repertoires are quite similar – the rabbit repertoire is different: Vκ-Domains • Rabbit kappa light chains contain an additional Cys in position L98,
which can form a disulfide bond with a Cys in CL
• Chothia canonical rules do not recognize most rabbit CDR L1s, although there is no reason why they should not assume the conformation appropriate to their length
• There is less length variability in CDR-L1 of rabbit Vκ domains than in human and murine kappa domains
• CDR L3 in rabbit Vκ lack Gln L108 (L90) and cis-Pro L136 (L?), which in human and murine Vκ domains produce the typical Ω-loop conformation. This produces a lambda-like CDR-L3 which might increase the flexibility of the VL/VH interface.
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CDR 1 in murine/human antibodies
246 20 140 sequences Rabbit Vκ:
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CDR-Donors: Rabbit Antibodies Murine and human antibody repertoires are quite similar – the rabbit repertoire is different: Vκ-Domains • Rabbit kappa light chains contain an additional Cys in position L98,
which can form a disulfide bond with a Cys in CL
• Chothia canonical rules do not recognize most rabbit CDR L1s, although there is no reason why they should not assume the conformation appropriate to their length
• There is less length variability in CDR-L1 of rabbit Vκ domains than in human and murine kappa domains
• CDR L3 in rabbit Vκ lack Gln L108 (L90) and cis-Pro L136 (L?), which in human and murine Vκ domains produce the typical Ω-loop conformation. This produces a lambda-like CDR-L3 which might increase the flexibility of the VL/VH interface.
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CDR L3 in murine/human light chains
20 aa
42 21aa
143 22 aa
81 23 aa
120 24 aa
35 25 aa
11 26 aa
2 Rabbit Vκ
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CDR-Donors: Rabbit Antibodies VH-Domains • A’-strand (N-terminus) is frequently shortened by one residue • Upper core residue H2 is hydrophilic • Some VH domains have a flexible insertion (4 or 5 residues) in the kink
between strands A’ and A’’. • These VH domains have additional Cys residues in positions H22 (H21)
and H90 (H79) that can form a disulfide bond connecting strand B to strand F.
• Others have additional Cys in positions H42 (H?) and H57 (H50), allowing a disulfide bond that connects strands C and D.
• Some combine both additional disulfide bonds • Rabbit VH domains have a highly conserved additional Trp at the base of
CDR H2 • Rabbit VH domains show length variability in the outer loop
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H6
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CDR-Donors: Rabbit Antibodies VH-Domains • A’-strand (N-terminus) is frequently shortened by one residue • Upper core residue H2 is hydrophilic • Some VH domains have a flexible insertion (4 or 5 residues) in the kink
between strands A’ and A’’. • These VH domains have additional Cys residues in positions H22 (H21)
and H90 (H79) that can form a disulfide bond connecting strand B to strand F.
• Others have additional Cys in positions H42 (H?) and H57 (H50), allowing a disulfide bond that connects strands C and D.
• Some combine both additional disulfide bonds • Rabbit VH domains have a highly conserved additional Trp at the base of
CDR H2 • Rabbit VH domains show length variability in the outer loop
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Additional S-S bridges in VH
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CDR-Donors: Rabbit Antibodies VH-Domains • The A’-strand (N-terminus) is frequently shortened by one residue • Upper core residue H2 is hydrophilic • Some VH domains have a flexible insertion (4 or 5 residues) in the kink
between strands A’ and A’’. These VH domains have additional Cys residues in positions H22 and H90 that can form a disulfide bond connecting strand B to strand F.
• Others have additional Cys in positions H42 and H57, allowing a disulfide bond that connects strands C and D.
• Some combine both additional disulfide bonds • Rabbit VH domains have a highly conserved additional Trp at the base of
CDR H2 • Rabbit VH domains show length variability in the outer loop
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Trp H73(H62) Note CDR L3 conformation!
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CDR-Donors: Rabbit Antibodies VH-Domains • The A’-strand (N-terminus) is frequently shortened by one residue • Upper core residue H2 is hydrophilic • Some VH domains have a flexible insertion (4 or 5 residues) in the kink
between strands A’ and A’’. These VH domains have additional Cys residues in positions H22 and H90 that can form a disulfide bond connecting strand B to strand F.
• Others have additional Cys in positions H42 and H57, allowing a disulfide bond that connects strands C and D.
• Some combine both additional disulfide bonds • Rabbit VH domains have a highly conserved additional Trp at the base of
CDR H2 • Rabbit VH domains show length variability in the outer loop
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Outer Loops
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Why did those CDR Grafts fail?
Go to Graft Designer