VanabinP, a novel vanadium-binding protein in the blood plasma of an ascidian, Ascidia sydneiensis same
Biochimica et Biophysica Acta Volume 1730
Page 206-217
published_at 2005
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Title ( eng ) |
VanabinP, a novel vanadium-binding protein in the blood plasma of an ascidian, Ascidia sydneiensis same
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Creator |
Yoshihara Masao
Watanabe Takahiro
Yamaguchi Nobuo
Kamino Kei
Michibata Hitoshi
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Source Title |
Biochimica et Biophysica Acta
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Volume | 1730 |
Start Page | 206 |
End Page | 217 |
Abstract |
Some ascidians accumulate high levels of the transition metal vanadium in their blood cells. The process of vanadium accumulation has not yet been elucidated. In this report, we describe the isolation and cDNA cloning of a novel vanadium-binding protein, designated as VanabinP, from the blood plasma of the vanadium-rich ascidian, Ascidia sydneiensis samea. The predicted amino acid sequence of VanabinP was highly conserved and similar to those of other Vanabins. The N-terminus of the mature form of VanabinP was rich in basic amino acid residues. VanabinP cDNA was originally isolated from blood cells, as were the other four Vanabins. However, Western blot analysis revealed that the VanabinP protein was localized to the blood plasma and was not detectable in blood cells. RT-PCR analysis and in situ hybridization indicated that the VanabinP gene was transcribed in some cell types localized to peripheral connective tissues of the alimentary canal, muscle, blood cells, and a portion of the branchial sac. Recombinant VanabinP bound a maximum of 13 vanadium(IV) ions per molecule with a Kd of 2.8 × 10-5 M. These results suggest that VanabinP is produced in several types of cell, including blood cells, and is immediately secreted into the blood plasma where it functions as a vanadium(IV) carrier.
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Keywords |
Ascidian
Vanadium
Metal accumulation
Blood plasma
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NDC |
Biology [ 460 ]
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Language |
eng
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Resource Type | journal article |
Publisher |
Elsevier B.V.
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Date of Issued | 2005 |
Rights |
Copyright (c) 2005 Elsevier B.V.
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Publish Type | Author’s Original |
Access Rights | open access |
Source Identifier |
[ISSN] 0167-4781
[NCID] AA10506089
[PMID] 16084607
[DOI] 10.1016/j.bbaexp.2005.07.002
[DOI] http://dx.doi.org/10.1016/j.bbaexp.2005.07.002
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