2g60: Difference between revisions
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'''Structure of anti-FLAG M2 Fab domain'''<br /> | '''Structure of anti-FLAG M2 Fab domain'''<br /> | ||
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==About this Structure== | ==About this Structure== | ||
2G60 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:// | 2G60 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=2G60 OCA]. | ||
==Reference== | ==Reference== | ||
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[[Category: fab domain]] | [[Category: fab domain]] | ||
''Page seeded by [http:// | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Fri Feb 15 17:27:19 2008'' | ||
Revision as of 18:27, 15 February 2008
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Structure of anti-FLAG M2 Fab domain
OverviewOverview
The inherent difficulties of stabilizing detergent-solubilized integral, membrane proteins for biophysical or structural analysis demand the, development of new methodologies to improve success rates. One proven, strategy is the use of antibody fragments to increase the ;soluble', portion of any membrane protein, but this approach is limited by the, difficulties and expense associated with producing monoclonal antibodies, to an appropriate exposed epitope on the target protein. Here, the, stabilization of a detergent-solubilized K(+) channel protein, KvPae, by, engineering a FLAG-binding epitope into a known loop region of the protein, and creating a complex with Fab fragments from commercially available, anti-FLAG M2 monoclonal antibodies is reported. Although well diffracting, crystals of the complex have not yet been obtained, during the course of, crystallization trials the structure of the anti-FLAG M2 Fab domain was, solved to 1.86 A resolution. This structure, which should aid future, structure-determination efforts using this approach by facilitating, molecular-replacement phasing, reveals that the binding pocket appears to, be specific only for the first four amino acids of the traditional FLAG, epitope, namely DYKD. Thus, the use of antibody fragments for improving, the stability of target proteins can be rapidly applied to the study of, membrane-protein structure by placing the short DKYD motif within a, predicted peripheral loop of that protein and utilizing commercially, available anti-FLAG M2 antibody fragments.
About this StructureAbout this Structure
2G60 is a Protein complex structure of sequences from Mus musculus. Full crystallographic information is available from OCA.
ReferenceReference
Structure of anti-FLAG M2 Fab domain and its use in the stabilization of engineered membrane proteins., Roosild TP, Castronovo S, Choe S, Acta Crystallograph Sect F Struct Biol Cryst Commun. 2006 Sep 1;62(Pt, 9):835-9. Epub 2006 Aug 18. PMID:16946459
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