T. Hirasaki et al., PERMEATION MECHANISM OF DNA-MOLECULES IN SOLUTION THROUGH CUPRAMMONIUM REGENERATED CELLULOSE HOLLOW-FIBER (BMM(TM)), Journal of membrane science, 106(1-2), 1995, pp. 123-129
We tried to clarify the membrane permeation mechanism of biopolymer DN
A molecule in solution through cuprammonium regenerated cellulose holl
ow fiber (BMM(TM)) from the dependence of the permeability of the DNA
molecule on the molecular weight (MW), the transmembrane pressure (Del
ta P), the total challenge dose, the original concentration of DNA and
on the conformation of DNA and from the observation of the shape of t
he DNA molecule remaining in the membrane wall. The shape of the DNA m
olecule was observed using transmission electron microscopy (TEM), The
permeability of DNA molecules decreased with an increase in the MW of
the DNA molecule. The MW of the molecule which showed a permeability
of more than 0.9 was 1 X 10(6) for the protein with global configurati
on and 1 x 10(8) for DNA, The linear protein of the blood coagulation
factor VIII combined with von Willebrand factor (F-VIII with VWF) with
MW of 2 X 10(7) showed a permeability similar to that of DNA rather t
han that of the global protein, When Delta P decreased, the permeabili
ty of DNA decreased. Electron microscope observation showed that the D
NA molecules were elongated by the shear stress originated in the flow
of the solution in pores. We can conclude that: (1) Protein and DNA p
ermeate through BMM mainly based on sieving effects. (2) The molecules
of DNA and F-VIII with VWF are considered to deform into a string sha
pe along the stream line. The chemical structure of a molecule and the
shear stress of filtration govern its deformability. The deformation
of the molecule contributes to the permeability through BMM, (3) The s
ieving effect in working on the permeation of molecules should take in
to account their deformability in addition to their geometrical size.