Solution Structure of the Link Module: A Hyaluronan-Binding Domain Involved in Extracellular Matrix Stability and Cell Migration

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...

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Veröffentlicht in:Cell 1996-09, Vol.86 (5), p.767-775
Hauptverfasser: Kohda, Daisuke, Morton, Craig J, Parkar, Ashfaq A, Hatanaka, Hideki, Inagaki, Fuyuhiko M, Campbell, Iain D, Day, Anthony J
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Sprache:eng
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Zusammenfassung: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.
ISSN:0092-8674
1097-4172
DOI:10.1016/S0092-8674(00)80151-8