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. 2012 Apr 30;287(25):20774–20783. doi: 10.1074/jbc.M111.320069

TABLE 1.

Summary of the polysaccharide and oligosaccharide constructs

Constructs Anticipated disaccharide repeating unit Size of the construct Modification steps involved 35S labeling site
1 (-GlcA-GlcNS-)n Polysaccharide, >6,000 Da NST N-[35S]sulfation
2 (-GlcA-GlcNS6S-)n Polysaccharide, >6,000 Da NST and 6-OST N-[35S]sulfation
3 (-IdoA-GlcNS6S-)n Polysaccharide, >6,000 Da NST, C5-epi, and 6-OST N-[35S]sulfation
4 (-GlcA2S-GlcNS-)n Polysaccharide, >6,000 Da NST and 2-OST N-[35S]sulfation
5 (-IdoA2S-GlcNS-)n Polysaccharide, >6,000 Da NST, C5-epi, and 2-OST N-[35S]sulfation
6 (-IdoA2S-GlcNS6S-)n Polysaccharide, >6,000 Da NST, C5-epi, 2-OST, and 6-OST N-[35S]sulfation
7 (-GlcA2S-GlcNS6S-)n Polysaccharide, >6,000 Da NST, 2-OST, and 6-OST N-[35S]sulfation
8 (-GlcA-GlcNS ± 6S ± 3S-)n and (-IdoA2S-GlcNS6S-)m Polysaccharide, >6,000 Da NST, C5-epi, 2-OST, 6-OST, and 3-OST-1 N-[35S]sulfation
9 (-GlcA2S-GlcNS6S-)n and (-GlcA-GlcNS ± 6S ± 3S-)m Polysaccharide, >6,000 Da NST, 2-OST, 6-OST, and 3-OST-1 N-[35S]sulfation
10 Heparin, (-IdoA2S-GlcNS6S-)n and (-GlcA-GlcNS ± 6S ± 3S-)m Polysaccharide, >6,000 Da 3-OST-5 3-O-[35S]sulfation
11 GlcNAc6S-GlcA-GlcNS6S3S-IdoA2S-GlcNS6S-GlcA-AnMan Heptasaccharide (7-mer) Synthesis started from pure N-sulfo, N-acetylated heptasaccharide 3-O-[35S]sulfation
12a GlcA-GlcNS6S- (IdoA ± 2S-GlcNS6S)2-GlcA-AnMan Octasaccharide (8-mer no 3-O-sulfation) Synthesis started from pure N-sulfo octasaccharide N-[35S]sulfation
12b GlcA-GlcNS6S ± 3S- (IdoA ± 2S-GlcNS6S)2-GlcA-AnMan Octasaccharide (8-mer with 3-O-sulfation) Synthesis started from pure N-sulfo octasaccharide N-[35S]sulfation
13a GlcNS6S-GlcA-GlcNS6S- (IdoA ± 2S-GlcNS6S)2-GlcA-AnMan Nonasaccharide (9-mer no 3-O-sulfation) Synthesis started from pure N-sulfo nonasaccharide N-[35S]sulfation
13b GlcNS6S-GlcA-GlcNS6S ± 3S- (IdoA ± 2S-GlcNS6S)2-GlcA-AnMan Nonasaccharide (9-mer with 3-O-sulfation) Synthesis started from pure N-sulfo nonasaccharide N-[35S]sulfation
14 GlcA-GlcNS6S ± 3S- (GlcA ± 2S-GlcNS6S)3-GlcA-AnMan Decasaccharide (10-mer no IdoA) Synthesis started from pure N-sulfo decasaccharide 6-O-[35S]sulfation
15a GlcA-GlcNS6S- (IdoA ± 2S-GlcNS6S)3-GlcA-AnMan Decasaccharide (10-mer no 3-O-sulfation) Synthesis started from pure N-sulfo decasaccharide 6-O-[35S]sulfation
15b GlcA-GlcNS6S ± 3S- (IdoA ± 2S-GlcNS6S)3-GlcA-AnMan Decasaccharide (10-mer with 3-O-sulfation) Synthesis started from pure N-sulfo decasaccharide 6-O-[35S]sulfation
16 GlcA-GlcNS6S ± 3S- (GlcA ± 2S-GlcNS6S)4-GlcA-AnMan Dodecasaccharide (12-mer no IdoA) Synthesis started from pure N-sulfo dodecasaccharide 6-O-[35S]sulfation
17a GlcA-GlcNS6S- (IdoA ± 2S-GlcNS6S)4-GlcA-AnMan Dodecasaccharide (12-mer no 3-O-sulfation) Synthesis started from pure N-sulfo decasaccharide 6-O-[35S]sulfation
17b GlcA-GlcNS6S ± 3S- (IdoA ± 2S-GlcNS6S)4-GlcA-AnMan Dodecasaccharide (12-mer with 3-O-sulfation) Synthesis started from pure N-sulfo decasaccharide 6-O-[35S]sulfation
18 GlcNS6S- (GlcA ± 2S-GlcNS6S ± 3S)3- (GlcA-GlcNAc6S)2-GlcA-GlcNS6S-GlcA-AnMan Pentadecasaccharide (15-mer no IdoA) Synthesis started from pure N-sulfo, N-acetylated pentadecasaccharide 6-O-[35S]sulfation
19 GlcNS6S- (IdoA ± 2S-GlcNS6S ± 3S)3- (GlcA-GlcNAc6S)2-GlcA-GlcNS6S-GlcA-AnMan Pentadecasaccharide (15-mer) Synthesis started from pure N-sulfo, N-acetylated pentadecasaccharide 6-O-[35S]sulfation
20 GlcNAc6S- (GlcA ± 2S-GlcNS6S ± 3S)4- (GlcA-GlcNAc6S)2-GlcA-GlcNS6S-GlcA-AnMan Heptadecasaccharide (17-mer no IdoA) Synthesis started from pure N-sulfo, N-acetylated heptadecasaccharide 6-O-[35S]sulfation
21 GlcNAc6S- (IdoA2S-GlcNS6S ± 3S)4- (GlcA-GlcNAc6S)2-GlcA-GlcNS6S-GlcA-AnMan Heptadecasaccharide (17-mer) Synthesis started from pure N-sulfo, N-acetylated heptadecasaccharide 6-O-[35S]sulfation
22 GlcNS6S- (IdoA2S-GlcNS6S ± 3S)5- (GlcA-GlcNAc6S)2-GlcA-GlcNS6S-GlcA-AnMan Nonadecasaccharide (19-mer no IdoA) Synthesis started from pure N-sulfo, N-acetylated nonadecasaccharide 6-O-[35S]sulfation
23 GlcNS6S- (IdoA2S-GlcNS6S ± 3S)5- (GlcA-GlcNAc6S)2-GlcA-GlcNS6S-GlcA-AnMan Nonadecasaccharide (19-mer) Synthesis started from pure N-sulfo, N-acetylated nonadecasaccharide 6-O-[35S]sulfation