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   <subfield code="a">10.1007/PL00000627</subfield>
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   <subfield code="a">(NATIONALLICENCE)springer-10.1007/PL00000627</subfield>
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   <subfield code="a">Renkonen</subfield>
   <subfield code="D">O.</subfield>
   <subfield code="u">Institute of Biotechnology, University of Helsinki, P.O. Box 56 FIN-00014 (Finland), Fax +358 9 191 59563, e-mail: ossi.renkonen@helsinki.fi, FI</subfield>
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   <subfield code="a">Enzymatic in vitro synthesis of I-branches of mammalian polylactosamines: generation of scaffolds for multiple selectin-binding saccharide determinants</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[O. Renkonen]</subfield>
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  <datafield tag="520" ind1="3" ind2=" ">
   <subfield code="a">Abstract.: Polylactosamines are covalent monosaccharide assemblies of the animal kingdom and some bacteria, and are characterized by backbones of interlinked N-acetyllactosamine units (Galβ1-4GlcNAc, LacNAc). The mammalian LacNAc arrays are linear (blood group i-type) and branched (blood group I-type), and are linked to the core elements of glycolipids as well as O- and N-glycans of glycoproteins and keratan sulfate proteoglycans. Generation of I-branches to linear i-type polylactosamines is initiated by two kinds of β6GlcNAc transferases. One type of the enzymes transfers to GlcNAcβ1-3Galβ1-OR of growing i-chains at the peridistal (underlined) Gal; these enzymes are called dIGnT (d for ‘distally acting'). The other enzymes transfer to internal Gal units of preformed i-chains; they are called cIGnT (c for ‘centrally acting'). Purified natural and recombinant enzymes of both types have been described. The structures of I-type polylactosamines result from a collaboration of dIGnTs, cIGnTs, β4GalTs and the i-chain-elongating iGnTs. At present, the interplay of these enzymes in vivo is poorly understood. By contrast, enzyme-assisted in vitro synthesis of branched polylactosamines representing distinct LacNAc arrays that are multiply capped by a variety of decorations is possible. Some of the synthetic polylactosamines reduce the lymphocyte-endothelium adhesion in a tissue-specific mode, raising the possibility of achieving local immunosuppression in the future. Useful applications of multiply decorated I-type polylactosamines may also be found in prevention of mammalian gamete adhesion and in inhibition of bacterial and viral adhesion to host tissues.</subfield>
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  <datafield tag="540" ind1=" " ind2=" ">
   <subfield code="a">Birkhäuser Verlag Basel,, 2000</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">Key words. Polylactosamines</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">polylactosaminoglycans</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">poly-N-acetyllactosamines</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">i-antigens</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">I-antigens</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">biosynthesis</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">enzyme-assisted synthesis</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">in vitro synthesis</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">branched backbones</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">cell adhesion</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">selectin ligands</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">anti-inflammatory saccharides</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">endothelial saccharides</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">sialyl Lewis x</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">Lex</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">sialyl diLex</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">sialyl diLex</subfield>
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   <subfield code="a">lymphocyte extravasation</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">L-selectin</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">allograft rejection</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">site-specific immunosuppression</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">lymph nodes</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">inflammation</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">IGnT</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">β6GlcNAcT</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">Renkonen</subfield>
   <subfield code="D">O.</subfield>
   <subfield code="u">Institute of Biotechnology, University of Helsinki, P.O. Box 56 FIN-00014 (Finland), Fax +358 9 191 59563, e-mail: ossi.renkonen@helsinki.fi, FI</subfield>
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   <subfield code="a">Metadata rights reserved</subfield>
   <subfield code="b">Springer special CC-BY-NC licence</subfield>
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