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J. Biol. Chem., Vol. 263, Issue 28, 14196-14202, Oct, 1988
P Graceffa, CL Wang and WF Stafford
A wide range of values has been reported for the subunit and molecular
weights of smooth muscle caldesmon. There have also been conflicting
reports concerning whether caldesmon is a monomer or dimer. We attempted to
resolve these uncertainties by determining the molecular weight of chicken
gizzard smooth muscle caldesmon using the technique of sedimentation
equilibrium in the analytical ultracentrifuge. Unlike previous methods that
have been used to estimate the molecular weight of caldesmon, the molecular
weight determined by equilibrium sedimentation does not depend upon
assumptions about the shape of the molecule. We concluded that caldesmon in
solution is monomeric with a molecular mass of 93 +/- 4 kDa, a value that
is much less than those previously reported in the literature. This new
value, in conjunction with sedimentation velocity experiments, led to the
conclusion that caldesmon is a highly asymmetric molecule with an apparent
length of 740 A in solution. The mass of a cyanogen bromide fragment, with
an apparent mass of 37 kDa from sodium dodecyl sulfate-polyacrylamide gel
electrophoresis, was determined to be 25.1 +/- 0.6 kDa using sedimentation
equilibrium. These results imply that the reported molecular weights of
other fragment(s) of caldesmon have also been overestimated. We have
determined an optical extinction coefficient for caldesmon (E1%(280 nm) =
3.3) by determining its concentration from its refractive index which was
measured in the analytical ultracentrifuge. From the above values of the
molecular weight and the extinction coefficient, we redetermined that the
caldesmon molecule has two cysteines and recalculated the stoichiometric
molar ratio of actin/tropomyosin/caldesmon in the smooth muscle thin
filament to be 28:4:1.
Caldesmon. Molecular weight and subunit composition by analytical ultracentrifugation
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