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J Biol Chem, Vol. 273, Issue 17, 10602-10608, April 24, 1998
From the We have investigated the oligomerization process
of tenascin-C using a variety of recombinant wild-type and mutant
polypeptide chain fragments produced by heterologous gene expression in
Escherichia coli. Biochemical and biophysical analyses of
the structures and assemblies of these fragments indicated a sequential
two-step oligomerization mechanism of tenascin-C involving the
concerted interaction of two distinct domains and cysteines 64, 111, and 113. First, the sequence between alanine 114 and glutamine 139 initiates hexabrachion formation via a parallel three-stranded coiled
coil. Subsequently, the tenascin assembly domain, which is unique to
the tenascins, is responsible for the connection of two triplets to a
hexamer. The oligomerization of the tenascin assembly domains by the
three-stranded coiled coil increases their homophilic binding affinity
and is an important prerequisite for tenascin-C hexamerization.
Although formation of the characteristic hexabrachion structure
involves the covalent linkage of the six subunits by cysteine residues,
mutational analysis indicates that hexamer formation is not dependent
on intermolecular disulfide bonds. Most interestingly, substitution of
glutamate 130 within the coiled-coil domain by leucine or alanine
resulted in the formation of parallel four-stranded helix structures,
which further associated to dodecamers. Aside from supporting a
sequential process of tenascin-C assembly, this finding provides
experimental evidence that non-core residues can have profound effects
on the oligomerization states of coiled coils.
Tenascin-C Hexabrachion Assembly Is a Sequential Two-step Process
Initiated by Coiled-coil
-Helices
,
,
,
,
Department of Biophysical Chemistry,
Copyright © 1998 by The American Society for Biochemistry and Molecular Biology, Inc.
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