Solution structure of the link module: A hyaluronan-binding domain involved in extracellular matrix stability and cell migration

Daisuke Kohda, Craig J. Morton, Ashfaq A. Parkar, Hideki Hatanaka, Fuyuhiko M. Inagaki, Iain D. Campbell, Anthony J. Day

    Research output: Contribution to journalArticlepeer-review

    Abstract

    Link modules are hyaluronan-binding domains found in proteins involved in the assembly of extracellular matrix, cell adhesion, and migration. The solution structure of the Link module from human TSG-6 was determined and found to consist of two α helices and two antiparallel β sheets arranged around a large hydrophobic core. This defines the consensus fold for the Link module superfamily, which includes CD44, cartilage link protein, and aggrecan. The TSG-6 Link module was shown to interact with hyaluronan, and a putative binding surface was identified on the structure. A structural database search revealed close similarity between the Link module and the C- type lectin domain, with the predicted hyaluronan-binding site at an analogous position to the carbohydrate-binding pocket in E-selectin.
    Original languageEnglish
    Pages (from-to)767-775
    Number of pages8
    JournalCell
    Volume86
    Issue number5
    DOIs
    Publication statusPublished - 6 Sept 1996

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