1wt5

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(New page: 200px<br /> <applet load="1wt5" size="450" color="white" frame="true" align="right" spinBox="true" caption="1wt5, resolution 2.10&Aring;" /> '''The Crystal Structu...)
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'''The Crystal Structure Of A Humanized Antibody Fv 528'''<br />
'''The Crystal Structure Of A Humanized Antibody Fv 528'''<br />
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==About this Structure==
==About this Structure==
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1WT5 is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1WT5 OCA].
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1WT5 is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1WT5 OCA].
==Reference==
==Reference==
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[[Category: immune system]]
[[Category: immune system]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Sun Nov 18 09:44:07 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Jan 23 12:30:36 2008''

Revision as of 10:30, 23 January 2008


1wt5, resolution 2.10Å

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The Crystal Structure Of A Humanized Antibody Fv 528

Overview

To investigate the role of Vernier zone residues, which are comprised in, the framework regions and underlie the complementarity-determining regions, (CDRs) of antibodies, in the specific, high-affinity interactions of, antibodies with their targets, we focused on the variable domain fragment, of murine anti-human epidermal growth factor receptor (EGFR) antibody 528, (m528Fv). Grafting of the CDRs of m528Fv onto a selected framework region, of human antibodies, referred to as humanization, reduced the antibody's, affinity for its target by a factor of 1/40. The reduction in affinity was, due to a substantial reduction in the negative enthalpy change associated, with binding. Crystal structures of the ligand-free antibody fragments, showed no noteworthy conformational changes due to humanization, and the, loop structures of the CDRs of the humanized antibodies were identical to, those of the parent antibodies. Several mutants of the CDR-grafted, (humanized) variable domain fragment (h528Fv), in which some of the, Vernier zone residues in the heavy chain were replaced with the parental, murine residues, were constructed and prepared using a bacterial, expression system. Thermodynamic analyses of the interactions between the, mutants and the soluble extracellular domain of EGFR showed that several, single mutations and a double mutation increased the negative enthalpy and, heat capacity changes. Combination of these mutations, however, led to, somewhat reduced negative enthalpy and heat capacity changes. The affinity, of each mutant for the target was within the range for the wild-type, h528Fv, and this similarity was due to enthalpy-entropy compensation., These results suggest that Vernier zone residues make enthalpic, contributions to antigen binding and that the regulation of conformational, entropy changes upon humanization of murine antibodies must be carefully, considered and optimized.

About this Structure

1WT5 is a Protein complex structure of sequences from Homo sapiens. Full crystallographic information is available from OCA.

Reference

Thermodynamic consequences of mutations in Vernier zone residues of a humanized anti-human epidermal growth factor receptor (EGFR) murine antibody, 528., Makabe K, Nakanishi T, Tsumoto K, Tanaka Y, Kondo H, Umetsu M, Sone Y, Asano R, Kumagai I, J Biol Chem. 2007 Oct 17;. PMID:17947238

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