1p4i

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(New page: 200px<br /> <applet load="1p4i" size="450" color="white" frame="true" align="right" spinBox="true" caption="1p4i, resolution 2.8&Aring;" /> '''Crystal Structure of...)
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<applet load="1p4i" size="450" color="white" frame="true" align="right" spinBox="true"
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caption="1p4i, resolution 2.8&Aring;" />
'''Crystal Structure of scFv against peptide GCN4'''<br />
'''Crystal Structure of scFv against peptide GCN4'''<br />
==Overview==
==Overview==
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We generated a single chain Fv fragment of an antibody (scFv) with a, binding affinity of about 5 pm to a short peptide by applying rigorous, directed evolution. Starting from a high affinity peptide binder, originally obtained by ribosome display from a murine library, we, generated libraries of mutants with error-prone PCR and DNA shuffling and, applied off-rate selection by using ribosome display. Crystallographic, analysis of the scFv in its antigen-bound and free state showed that only, few mutations, which do not make direct contact to the antigen, lead to a, 500-fold affinity improvement over its potential germ line precursor., These results suggest that the affinity optimization of very high affinity, binders is achieved by modulating existing interactions via subtle changes, in the framework rather than by introducing new contacts. Off-rate, selection in combination with ribosome display can evolve binders to the, low picomolar affinity range even for peptide targets.
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We generated a single chain Fv fragment of an antibody (scFv) with a binding affinity of about 5 pm to a short peptide by applying rigorous directed evolution. Starting from a high affinity peptide binder, originally obtained by ribosome display from a murine library, we generated libraries of mutants with error-prone PCR and DNA shuffling and applied off-rate selection by using ribosome display. Crystallographic analysis of the scFv in its antigen-bound and free state showed that only few mutations, which do not make direct contact to the antigen, lead to a 500-fold affinity improvement over its potential germ line precursor. These results suggest that the affinity optimization of very high affinity binders is achieved by modulating existing interactions via subtle changes in the framework rather than by introducing new contacts. Off-rate selection in combination with ribosome display can evolve binders to the low picomolar affinity range even for peptide targets.
==About this Structure==
==About this Structure==
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1P4I is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Mus_musculus Mus musculus]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1P4I OCA].
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1P4I is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Mus_musculus Mus musculus]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1P4I OCA].
==Reference==
==Reference==
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[[Category: scfv]]
[[Category: scfv]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Sun Nov 18 09:39:35 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 14:24:58 2008''

Revision as of 12:24, 21 February 2008


1p4i, resolution 2.8Å

Drag the structure with the mouse to rotate

Crystal Structure of scFv against peptide GCN4

Overview

We generated a single chain Fv fragment of an antibody (scFv) with a binding affinity of about 5 pm to a short peptide by applying rigorous directed evolution. Starting from a high affinity peptide binder, originally obtained by ribosome display from a murine library, we generated libraries of mutants with error-prone PCR and DNA shuffling and applied off-rate selection by using ribosome display. Crystallographic analysis of the scFv in its antigen-bound and free state showed that only few mutations, which do not make direct contact to the antigen, lead to a 500-fold affinity improvement over its potential germ line precursor. These results suggest that the affinity optimization of very high affinity binders is achieved by modulating existing interactions via subtle changes in the framework rather than by introducing new contacts. Off-rate selection in combination with ribosome display can evolve binders to the low picomolar affinity range even for peptide targets.

About this Structure

1P4I is a Protein complex structure of sequences from Mus musculus. Full crystallographic information is available from OCA.

Reference

Directed in vitro evolution and crystallographic analysis of a peptide-binding single chain antibody fragment (scFv) with low picomolar affinity., Zahnd C, Spinelli S, Luginbuhl B, Amstutz P, Cambillau C, Pluckthun A, J Biol Chem. 2004 Apr 30;279(18):18870-7. Epub 2004 Jan 30. PMID:14754898

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