A Visualizable Chain-Terminating Inhibitor of Glycosaminoglycan Biosynthesis in Developing Zebrafish

被引:40
作者
Beahm, Brendan J. [1 ]
Dehnert, Karen W. [1 ]
Derr, Nicolas L. [2 ,3 ,4 ]
Kuhn, Joachim [5 ]
Eberhart, Johann K. [6 ]
Spillmann, Dorothe [7 ]
Amacher, Sharon L. [2 ,3 ,4 ]
Bertozzi, Carolyn R. [1 ]
机构
[1] Univ Calif Berkeley, Howard Hughes Med Inst, Dept Chem & Mol & Cell Biol, Berkeley, CA 94720 USA
[2] Ohio State Univ, Dept Mol Genet, Columbus, OH 43210 USA
[3] Ohio State Univ, Dept Mol & Cellular Biochem, Columbus, OH 43210 USA
[4] Ohio State Univ, Ctr RNA Biol, Columbus, OH 43210 USA
[5] Herz & Diabet Zentrum Nordrhein Westfalen, Inst Labs & Transfus Med, D-32545 Bad Oeynhausen, Germany
[6] Univ Texas Austin, Dept Mol Biosci, Austin, TX 78713 USA
[7] Uppsala Univ, Biomed Ctr, Dept Med Biochem & Microbiol, S-75123 Uppsala, Sweden
关键词
biosynthesis; click chemistry; glycosaminoglycans; inhibitors; zebrafish; HEPARAN-SULFATE BIOSYNTHESIS; CHONDROITIN SULFATE; TUMOR SUPPRESSORS; LAMININS; GLYCANS; IDENTIFICATION; GLYCOSYLATION; PROTEOGLYCANS; MORPHOGENESIS; GASTRULATION;
D O I
10.1002/anie.201310569
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Heparan sulfate (HS) and chondroitin sulfate (CS) glycosaminoglycans (GAG) are proteoglycan-associated polysaccharides with essential functions in animals. They have been studied extensively by genetic manipulation of biosynthetic enzymes, but chemical tools for probing GAG function are limited. HS and CS possess a conserved xylose residue that links the polysaccharide chain to a protein backbone. Here we report that, in zebrafish embryos, the peptide-proximal xylose residue can be metabolically replaced with a chain-terminating 4-azido-4-deoxyxylose (4-XylAz) residue by administration of UDP-4-azido-4-deoxyxylose (UDP-4-XylAz). UDP-4-XylAz disrupted both HS and CS biosynthesis and caused developmental abnormalities reminiscent of GAG biosynthesis and laminin mutants. The azide substituent of protein-bound 4-XylAz allowed for rapid visualization of the organismal sites of chain termination invivo through bioorthogonal reaction with fluorescent cyclooctyne probes. UDP-4-XylAz therefore complements genetic tools for studies of GAG function in zebrafish embryogenesis.
引用
收藏
页码:3347 / 3352
页数:6
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