Crystal structure and immunological properties of the first annexin from Schistosoma mansoni: insights into the structural integrity of the schistosomal tegument. (15th January 2014)

• Record Type: Journal Article
• Authors: Leow, Chiuan Yee; Willis, Charlene; Osman, Asiah; Mason, Lyndel; Simon, Anne; Smith, Brian J.; Gasser, Robin B.; Jones, Malcolm K.; Hofmann, Andreas
• Is Part Of: FEBS journal. Volume 281:Number 4(2014)
• Page Start: 1209
• Page End: 1225
• Publication Date: 2014-01-15
• Subjects: Biochemistry -- Periodicals; Molecular biology -- Periodicals; Pathology, Molecular -- Periodicals; 572
• DOI: 10.1111/febs.12700
• Languages: English
• ISSNs: 1742-464X

Abstract

<abstract abstract-type="main" id="febs12579-abs-0001"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="febs12700-sec-0001" sec-type="section"> <p>Schistosomiasis is a major parasitic disease of humans, second only to malaria in its global impact. The disease is caused by digenean trematodes that infest the vasculature of their human hosts. These flukes are limited externally by a body wall composed of a syncytial epithelium, the apical surface membrane of which is a parasitism‐adapted dual membrane complex. Annexins are thought to be of integral importance for the stability of this apical membrane system. Here, we present the first structural and immunobiochemical characterization of an annexin from <italic>Schistosoma mansoni</italic>. The crystal structure of annexin B22 confirms the presence of the previously predicted α‐helical segment in the II/III linker and reveals a covalently linked head‐to‐head dimer. From the calcium‐bound crystal structure of this protein, canonical type II, type III and B site positions are occupied, and a novel binding site has been identified. The dimer arrangement observed in the crystal structure suggests the presence of two prominent features, a potential non‐canonical membrane binding site and a potential binding groove opposite to the former. Results from transcriptional profiling during development show that annexin B22 expression is correlated with life stages of the parasite that possess the syncytial tegument layer, and ultrastructural localization by immuno‐electron microscopy confirms the occurrence of annexins in the tegument of <italic>S. mansoni</italic>. Data from membrane binding and aggregation assays indicate the presence of differential molecular mechanisms and support the hypothesis of annexin B22 providing structural integrity in the tegument.</p> </sec> <sec id="febs12700-sec-0002" sec-type="section"> <title>Database</title> <p>Coordinates and structure factors have been deposited with the PDB, accession numbers <ext-link ext-link-type="uri" xlink:href="http://www.rcsb.org/pdb/search/structidSearch.do?structureId=4mdu" xlink:type="simple" xmlns:xlink="http://www.w3.org/1999/xlink">4mdu</ext-link>, <ext-link ext-link-type="uri" xlink:href="http://www.rcsb.org/pdb/search/structidSearch.do?structureId=4mdv" xlink:type="simple" xmlns:xlink="http://www.w3.org/1999/xlink">4mdv</ext-link></p> </sec> <sec id="febs12700-sec-0003" sec-type="section"> <title>Structured digital abstract</title> <p> <list id="febs12700-list-0001" list-type="bullet"> <list-item> <p> <ext-link ext-link-type="uri" xlink:href="http://www.uniprot.org/uniprot/C4QH88" xlink:type="simple" xmlns:xlink="http://www.w3.org/1999/xlink">annexin B22</ext-link> and <ext-link ext-link-type="uri" xlink:href="http://www.uniprot.org/uniprot/C4QH88" xlink:type="simple" xmlns:xlink="http://www.w3.org/1999/xlink">annexin B22</ext-link><ext-link ext-link-type="uri" xlink:href="http://www.ebi.ac.uk/ontology-lookup/?termId=MI:0407" xlink:type="simple" xmlns:xlink="http://www.w3.org/1999/xlink">bind</ext-link> by <ext-link ext-link-type="uri" xlink:href="http://www.ebi.ac.uk/ontology-lookup/?termId=MI:0071" xlink:type="simple" xmlns:xlink="http://www.w3.org/1999/xlink">molecular sieving</ext-link> (<ext-link ext-link-type="uri" xlink:href="http://www.ebi.ac.uk/intact/interaction/EBI-9073331" xlink:type="simple" xmlns:xlink="http://www.w3.org/1999/xlink">View interaction</ext-link>)</p> </list-item> <list-item> <p> <ext-link ext-link-type="uri" xlink:href="http://www.uniprot.org/uniprot/C4QH88" xlink:type="simple" xmlns:xlink="http://www.w3.org/1999/xlink">annexin B22</ext-link> and <ext-link ext-link-type="uri" xlink:href="http://www.uniprot.org/uniprot/C4QH88" xlink:type="simple" xmlns:xlink="http://www.w3.org/1999/xlink">annexin B22</ext-link> <ext-link ext-link-type="uri" xlink:href="http://www.ebi.ac.uk/ontology-lookup/?termId=MI:0407" xlink:type="simple" xmlns:xlink="http://www.w3.org/1999/xlink">bind</ext-link> by <ext-link ext-link-type="uri" xlink:href="http://www.ebi.ac.uk/ontology-lookup/?termId=MI:0114" xlink:type="simple" xmlns:xlink="http://www.w3.org/1999/xlink">x-ray crystallography</ext-link> (<ext-link ext-link-type="uri" xlink:href="http://www.ebi.ac.uk/intact/interaction/EBI-9073172" xlink:type="simple" xmlns:xlink="http://www.w3.org/1999/xlink">View interaction</ext-link>)</p> </list-item> </list> </p> </sec> </abstract>