Interaction of morin-cetyltrimethylammonium bromide with nucleic acids anddetermination of nucleic acids at nanograms per milliliter levels based onthe enhancement of preresonance light scattering
Rt. Liu et al., Interaction of morin-cetyltrimethylammonium bromide with nucleic acids anddetermination of nucleic acids at nanograms per milliliter levels based onthe enhancement of preresonance light scattering, ANALYST, 126(8), 2001, pp. 1367-1371
A new preresonance light scattering (PRLS) assay of nucleic acids is presen
ted. At pH 7.30, the weak PRLS of morin-cetyltrimethylammonium bromide (CTM
AB) can be greatly enhanced by the addition of nucleic acids, owing to the
interaction between the nucleic acid and morin-CTMAB. After the addition of
morin and CTMAB to DNA, the zeta potential of DNA decreases and changes fr
om negative to positive. which is due to the formation of an associate, the
aggregation of morin on nucleic acids and the electric neutralization betw
een DNA and the cationic surfactant CTMAB. Mechanism studies showed that th
e enhanced PRLS comes from the aggregation of morin in the presence of nucl
eic acids and CTMAB. The enhanced intensity of PRLS is in proportion to the
concentration of nucleic acids in the range 7.5 x 10(-9)-1.0 x 10(-5) g ml
(-1) for calf thymus DNA, 7.5 x 10(-9)-1.0 x 10(-6) g ml(-1) for salmon spe
rm DNA and 1.0 x 10(-8)-1.0 x 10(-6) g ml(-1) for yeast RNA. The detection
limits are 3.4, 6.2 and 4.1 ng ml(-1) for calf thymus DNA, salmon sperm DNA
and yeast RNA, respectively. Synthetic samples were analyzed satisfactoril
y.