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PMID: 8572310 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Biotinylated hyaluronic acid as a probe for identifying hyaluronic acid-binding proteins.

Analytical biochemistry ·Vol. 228 ·No. 2 ·1995-07-01 ·Pages 299-306

Yang B, Yang BL, Goetinck PF

Abstract

The glycosaminoglycans hyaluronan (HA), heparin, and chondroitin sulfate were biotinylated using biotin-x-hydrazide (biotin-epsilon-aminocaproyl hydrozyde) in conjunction with N-ethyl-N'-(3-dimethylaminopropyl)carbodiimide hydrochloride, an activating agent for carboxyl groups. The biotin-x-hydrazide was shown to be coupled directly to the glycosaminoglycans in enzymatic digestions and competition experiments. The biotinylated HA was shown to bind to link protein and receptor for hyaluronic acid-mediated motility, two proteins known to bind HA. The labeled HA was used as a probe to detect known HA-binding proteins in chicken cartilage extract and to identify new HA-binding motifs in the G3 domain of the proteoglycan aggrecan. The significance of the biotinylation of HA, heparin, and chondroitin sulfate A are discussed.

MeSH Terms
Binding, Competitive Biotin/chemistry Carbohydrate Sequence Chondroitin Sulfates/chemistry Heparin/chemistry Hyaluronan Receptors/analysis Hyaluronic Acid/chemistry Molecular Probes Molecular Sequence Data Molecular Structure
Chemicals
Hyaluronan Receptors Molecular Probes Biotin Hyaluronic Acid Heparin Chondroitin Sulfates
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Yang B
Cutaneous Biology Research Center, Massachusetts General Hospital, Harvard Medical School, Charlestown 02129, USA.
Yang B L
Goetinck P F
Article Info
Journal
Analytical biochemistry
Abbr.
Anal Biochem
ISSN
0003-2697
Published
1995-07-01
Pages
299-306
Language
English
Region
United States
NLM ID
0370535
Subset
IM
Grants
NICHD NIH HHS · HD 22016 · United States
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