Emerin is the protein of the inner nuclear membrane that is affected by mut
ation in X-linked Emery-Dreifuss muscular dystrophy. The autosomal dominant
form of the disease is caused by mutations in the lamin A/C gene. Several
lines of circumstantial evidence have suggested an interaction of emerin wi
th lamins in the nuclear lamina but direct interaction between the two prot
eins has not yet been demonstrated, me now demonstrate direct interaction b
etween recombinant emerin and lamin A molecules using biomolecular interact
ion analysis (BIA) and monoclonal antibodies. An emerin-lamin A interaction
system may be related in function to the LAP2-lamin B system at the inner
nuclear rim. (C) 2000 Academic Press.