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New page: left|200px<br /> <applet load="1qok" size="450" color="white" frame="true" align="right" spinBox="true" caption="1qok, resolution 2.4Å" /> '''MFE-23 AN ANTI-CARCI...
 
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[[Image:1qok.gif|left|200px]]<br />
[[Image:1qok.gif|left|200px]]<br /><applet load="1qok" size="350" color="white" frame="true" align="right" spinBox="true"  
<applet load="1qok" size="450" color="white" frame="true" align="right" spinBox="true"  
caption="1qok, resolution 2.4&Aring;" />
caption="1qok, resolution 2.4&Aring;" />
'''MFE-23 AN ANTI-CARCINOEMBRYONIC ANTIGEN SINGLE-CHAIN FV ANTIBODY'''<br />
'''MFE-23 AN ANTI-CARCINOEMBRYONIC ANTIGEN SINGLE-CHAIN FV ANTIBODY'''<br />


==Overview==
==Overview==
MFE-23 is the first single-chain Fv antibody molecule to be used in, patients and is used to target colorectal cancer through its high affinity, for carcinoembryonic antigen (CEA), a cell-surface member of the, immunoglobulin superfamily. MFE-23 contains an N-terminal variable, heavy-chain domain joined by a (Gly(4)Ser)(3) linker to a variable, light-chain (V(L)) domain (kappa chain) with an 11-residue C-terminal, Myc-tag. Its crystal structure was determined at 2.4 A resolution by, molecular replacement with an R(cryst) of 19.0%. Five of the six, antigen-binding loops, L1, L2, L3, H1 and H2, conformed to known canonical, structures. The sixth loop, H3, displayed a unique structure, with a, beta-hairpin loop and a bifurcated apex characterized by a buried Thr, residue. In the crystal lattice, two MFE-23 molecules were associated, back-to-back in a manner not seen before. The antigen-binding site, displayed a large acidic region located mainly within the H2 loop and a, large hydrophobic region within the H3 loop. Even though this structure is, unliganded within the crystal, there is an unusually large region of, contact between the H1, H2 and H3 loops and the beta-sheet of the V(L), domain of an adjacent molecule (strands DEBA) as a result of, intermolecular packing. These interactions exhibited remarkably high, surface and electrostatic complementarity. Of seven MFE-23 residues, predicted to make contact with antigen, five participated in these lattice, contacts, and this model for antigen binding is consistent with previously, reported site-specific mutagenesis of MFE-23 and its effect on CEA, binding.
MFE-23 is the first single-chain Fv antibody molecule to be used in patients and is used to target colorectal cancer through its high affinity for carcinoembryonic antigen (CEA), a cell-surface member of the immunoglobulin superfamily. MFE-23 contains an N-terminal variable heavy-chain domain joined by a (Gly(4)Ser)(3) linker to a variable light-chain (V(L)) domain (kappa chain) with an 11-residue C-terminal Myc-tag. Its crystal structure was determined at 2.4 A resolution by molecular replacement with an R(cryst) of 19.0%. Five of the six antigen-binding loops, L1, L2, L3, H1 and H2, conformed to known canonical structures. The sixth loop, H3, displayed a unique structure, with a beta-hairpin loop and a bifurcated apex characterized by a buried Thr residue. In the crystal lattice, two MFE-23 molecules were associated back-to-back in a manner not seen before. The antigen-binding site displayed a large acidic region located mainly within the H2 loop and a large hydrophobic region within the H3 loop. Even though this structure is unliganded within the crystal, there is an unusually large region of contact between the H1, H2 and H3 loops and the beta-sheet of the V(L) domain of an adjacent molecule (strands DEBA) as a result of intermolecular packing. These interactions exhibited remarkably high surface and electrostatic complementarity. Of seven MFE-23 residues predicted to make contact with antigen, five participated in these lattice contacts, and this model for antigen binding is consistent with previously reported site-specific mutagenesis of MFE-23 and its effect on CEA binding.


==About this Structure==
==About this Structure==
1QOK 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=1QOK OCA].  
1QOK 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=1QOK OCA].  


==Reference==
==Reference==
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[[Category: Mus musculus]]
[[Category: Mus musculus]]
[[Category: Protein complex]]
[[Category: Protein complex]]
[[Category: Begent, R.H.J.]]
[[Category: Begent, R H.J.]]
[[Category: Boehm, M.K.]]
[[Category: Boehm, M K.]]
[[Category: Chester, K.A.]]
[[Category: Chester, K A.]]
[[Category: Corper, A.L.]]
[[Category: Corper, A L.]]
[[Category: Keep, P.A.]]
[[Category: Keep, P A.]]
[[Category: Perkins, S.J.]]
[[Category: Perkins, S J.]]
[[Category: Sohi, M.K.]]
[[Category: Sohi, M K.]]
[[Category: Sutton, B.J.]]
[[Category: Sutton, B J.]]
[[Category: Thornton, J.D.]]
[[Category: Thornton, J D.]]
[[Category: Wan, T.]]
[[Category: Wan, T.]]
[[Category: anti-carcinoembryonic antigen]]
[[Category: anti-carcinoembryonic antigen]]
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[[Category: single-chain fv]]
[[Category: single-chain fv]]


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