Structure and purification of recombinant
layilin-Fc fusion protein. (A) The protein domains of the layilin-Fc
and wild-type layilin are shown. Layilin's extracellular part was
cloned immediately N-terminal to the hinge domain (H) of the human IgG1
so that the chimera contains two cysteine residues (not shown)
within the hinge domain responsible for Ig dimerization. Sig,
NH2-terminal signal sequence, Lectin, layilin's
extracellular part, which is homologous with C-type lectins; TM,
transmembrane domain; CH2 and CH3, constant regions of the human IgG.
(B) Purified layilin-Fc fusion protein was analyzed on an SDS-PAGE gel
under both reduced and nonreduced conditions and detected by
immunoblotting with the anti-human IgG (Fc-specific)
antibody. Molecular masses (in kDa) are shown at the left.