1i4a: Difference between revisions

New page: left|200px<br /><applet load="1i4a" size="450" color="white" frame="true" align="right" spinBox="true" caption="1i4a, resolution 2.0Å" /> '''CRYSTAL STRUCTURE OF ...
 
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[[Image:1i4a.gif|left|200px]]<br /><applet load="1i4a" size="450" color="white" frame="true" align="right" spinBox="true"  
[[Image:1i4a.gif|left|200px]]<br /><applet load="1i4a" size="350" color="white" frame="true" align="right" spinBox="true"  
caption="1i4a, resolution 2.0&Aring;" />
caption="1i4a, resolution 2.0&Aring;" />
'''CRYSTAL STRUCTURE OF PHOSPHORYLATION-MIMICKING MUTANT T6D OF ANNEXIN IV'''<br />
'''CRYSTAL STRUCTURE OF PHOSPHORYLATION-MIMICKING MUTANT T6D OF ANNEXIN IV'''<br />


==Overview==
==Overview==
Site-directed mutagenesis, electron microscopy, and X-ray crystallography, were used to probe the structural basis of annexin IV-induced membrane, aggregation and the inhibition of this property by protein kinase C, phosphorylation. Site-directed mutants that either mimic (Thr6Asp, T6D) or, prevent (Thr6Ala, T6A) phosphorylation of threonine 6 were produced for, these studies and compared with wild-type annexin IV. In vitro assays, showed that unmodified wild-type annexin IV and the T6A mutant, but not, PKC-phosphorylated wild-type or the T6D mutant, promote vesicle, aggregation. Electron crystallographic data of wild-type and T6D annexin, IV revealed that, similar to annexin V, the annexin IV proteins form 2D, trimer-based ordered arrays on phospholipid monolayers. Cryo-electron, microscopic images of junctions formed between lipid vesicles in the, presence of wild-type annexin IV indicated a separation distance, corresponding to the thickness of two layers of membrane-bound annexin IV., In this orientation, a single layer of WT annexin IV, attached to the, outer leaflet of one vesicle, would undergo face-to-face self-association, with the annexin layer of a second vesicle. The 2.0-A resolution crystal, structure of the T6D mutant showed that the mutation causes release of the, N-terminal tail from the protein core. This change would preclude the, face-to-face annexin self-association required to aggregate vesicles. The, data suggest that reversible complex formation through phosphorylation and, dephosphorylation could occur in vivo and play a role in the regulation of, vesicle trafficking following changes in physiological states.
Site-directed mutagenesis, electron microscopy, and X-ray crystallography were used to probe the structural basis of annexin IV-induced membrane aggregation and the inhibition of this property by protein kinase C phosphorylation. Site-directed mutants that either mimic (Thr6Asp, T6D) or prevent (Thr6Ala, T6A) phosphorylation of threonine 6 were produced for these studies and compared with wild-type annexin IV. In vitro assays showed that unmodified wild-type annexin IV and the T6A mutant, but not PKC-phosphorylated wild-type or the T6D mutant, promote vesicle aggregation. Electron crystallographic data of wild-type and T6D annexin IV revealed that, similar to annexin V, the annexin IV proteins form 2D trimer-based ordered arrays on phospholipid monolayers. Cryo-electron microscopic images of junctions formed between lipid vesicles in the presence of wild-type annexin IV indicated a separation distance corresponding to the thickness of two layers of membrane-bound annexin IV. In this orientation, a single layer of WT annexin IV, attached to the outer leaflet of one vesicle, would undergo face-to-face self-association with the annexin layer of a second vesicle. The 2.0-A resolution crystal structure of the T6D mutant showed that the mutation causes release of the N-terminal tail from the protein core. This change would preclude the face-to-face annexin self-association required to aggregate vesicles. The data suggest that reversible complex formation through phosphorylation and dephosphorylation could occur in vivo and play a role in the regulation of vesicle trafficking following changes in physiological states.


==About this Structure==
==About this Structure==
1I4A is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Bos_taurus Bos taurus] with CA and SO4 as [http://en.wikipedia.org/wiki/ligands ligands]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1I4A OCA].  
1I4A is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Bos_taurus Bos taurus] with <scene name='pdbligand=CA:'>CA</scene> and <scene name='pdbligand=SO4:'>SO4</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1I4A OCA].  


==Reference==
==Reference==
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[[Category: Brisson, A.]]
[[Category: Brisson, A.]]
[[Category: Campos, B.]]
[[Category: Campos, B.]]
[[Category: Dedman, J.R.]]
[[Category: Dedman, J R.]]
[[Category: Kaetzel, M.A.]]
[[Category: Kaetzel, M A.]]
[[Category: Mealy, T.R.]]
[[Category: Mealy, T R.]]
[[Category: Mo, Y.D.]]
[[Category: Mo, Y D.]]
[[Category: Seaton, B.A.]]
[[Category: Seaton, B A.]]
[[Category: CA]]
[[Category: CA]]
[[Category: SO4]]
[[Category: SO4]]
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[[Category: phosphorylation mutant]]
[[Category: phosphorylation mutant]]


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