1rjc: Difference between revisions

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New page: left|200px<br /> <applet load="1rjc" size="450" color="white" frame="true" align="right" spinBox="true" caption="1rjc, resolution 1.40Å" /> '''Crystal structure o...
 
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[[Image:1rjc.gif|left|200px]]<br />
[[Image:1rjc.gif|left|200px]]<br /><applet load="1rjc" size="350" color="white" frame="true" align="right" spinBox="true"  
<applet load="1rjc" size="450" color="white" frame="true" align="right" spinBox="true"  
caption="1rjc, resolution 1.40&Aring;" />
caption="1rjc, resolution 1.40&Aring;" />
'''Crystal structure of the camelid single domain antibody cAb-Lys2 in complex with hen egg white lysozyme'''<br />
'''Crystal structure of the camelid single domain antibody cAb-Lys2 in complex with hen egg white lysozyme'''<br />


==Overview==
==Overview==
A central paradigm in immunology states that successful generation of high, affinity antibodies necessitates an immense primary repertoire of, antigen-combining sites. Much of the diversity of this repertoire is, provided by varying one antigen binding loop, created by inserting, randomly a D (diversity) gene out of a small pool between the V and J, genes. It is therefore assumed that any particular D-encoded region, surrounded by different V and J regions adopts a different conformation., We have solved the structure of two lysozyme-specific variable domains of, heavy-chain antibodies isolated from two strictly unrelated dromedaries., These antibodies recombined identical D gene sequences to different V and, J precursors with significant variance in their V(D)J junctions. Despite, these large differences, the D-encoded loop segments adopt remarkably, identical architectures, thus directing the antibodies toward identical, epitopes. Furthermore, a striking convergent maturation process occurred, in the V region, adapting both binders for their sub-nanomolar affinity, association with lysozyme. Hence, on a structural level, humoral immunity, may rely more on well developed maturation and selection systems than on, the acquisition of large primary repertoires.
A central paradigm in immunology states that successful generation of high affinity antibodies necessitates an immense primary repertoire of antigen-combining sites. Much of the diversity of this repertoire is provided by varying one antigen binding loop, created by inserting randomly a D (diversity) gene out of a small pool between the V and J genes. It is therefore assumed that any particular D-encoded region surrounded by different V and J regions adopts a different conformation. We have solved the structure of two lysozyme-specific variable domains of heavy-chain antibodies isolated from two strictly unrelated dromedaries. These antibodies recombined identical D gene sequences to different V and J precursors with significant variance in their V(D)J junctions. Despite these large differences, the D-encoded loop segments adopt remarkably identical architectures, thus directing the antibodies toward identical epitopes. Furthermore, a striking convergent maturation process occurred in the V region, adapting both binders for their sub-nanomolar affinity association with lysozyme. Hence, on a structural level, humoral immunity may rely more on well developed maturation and selection systems than on the acquisition of large primary repertoires.


==About this Structure==
==About this Structure==
1RJC is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Camelus_dromedarius Camelus dromedarius] and [http://en.wikipedia.org/wiki/Gallus_gallus Gallus gallus] with PO4 and GOL as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Lysozyme Lysozyme], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.2.1.17 3.2.1.17] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1RJC OCA].  
1RJC is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Camelus_dromedarius Camelus dromedarius] and [http://en.wikipedia.org/wiki/Gallus_gallus Gallus gallus] with <scene name='pdbligand=PO4:'>PO4</scene> and <scene name='pdbligand=GOL:'>GOL</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Lysozyme Lysozyme], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.2.1.17 3.2.1.17] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1RJC OCA].  


==Reference==
==Reference==
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[[Category: Single protein]]
[[Category: Single protein]]
[[Category: Decanniere, K.]]
[[Category: Decanniere, K.]]
[[Category: Genst, E.De.]]
[[Category: Genst, E De.]]
[[Category: Ghahroudi, M.A.]]
[[Category: Ghahroudi, M A.]]
[[Category: Kinne, J.]]
[[Category: Kinne, J.]]
[[Category: Loris, R.]]
[[Category: Loris, R.]]
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[[Category: protein-protein hetero complex]]
[[Category: protein-protein hetero complex]]


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