Huang S C, Swerdlow H, Caldwell K D
Department of Chemical and Fuels Engineering, University of Utah, Salt Lake City 84112.
Anal Biochem. 1994 Nov 1;222(2):441-9. doi: 10.1006/abio.1994.1514.
The binding of 5'-end biotinylated DNA fragments was compared between streptavidin (SA)-coated commercial M-280 magnetic latex particles with a diameter of 2.8 microns and adsorption-coated polystyrene (PS) latex standard particles whose diameter is 0.272 microns. Amino acid analysis showed the protein content of the commercial particles to correspond to 4x monolayer coverage, while the adsorption-coated PS particles displayed monolayer coverage, or 8 pmol/cm2. A fluorescence-based method was developed to quantify the adsorption of FITC-labeled SA, biotin, and biotinylated DNA. The validity of the method was substantiated for the labeled protein by both amino acid analysis and a colorimetric protein assay. While the specific binding of biotin was 0.38 mol per mole of SA on the adsorption-coated 0.272-microns particles and slightly higher (0.6 mol per mole SA) on the 2.8-microns particles, the specific binding of the bulky biotinylated 300-bp DNA was more favorable on the smaller particle (0.12 mol per mole SA for 0.272 microns versus 0.04 mol per mole SA for 2.8 microns).
比较了直径为2.8微米的链霉亲和素(SA)包被的商用M-280磁性乳胶颗粒与直径为0.272微米的吸附包被聚苯乙烯(PS)乳胶标准颗粒对5'-端生物素化DNA片段的结合情况。氨基酸分析表明,商用颗粒的蛋白质含量相当于4倍单层覆盖,而吸附包被的PS颗粒显示为单层覆盖,即8 pmol/cm²。开发了一种基于荧光的方法来定量FITC标记的SA、生物素和生物素化DNA的吸附。通过氨基酸分析和比色蛋白测定法证实了该方法对标记蛋白的有效性。虽然生物素在吸附包被的0.272微米颗粒上与每摩尔SA的特异性结合为0.38摩尔,在2.8微米颗粒上略高(每摩尔SA为0.6摩尔),但体积较大的生物素化300-bp DNA在较小颗粒上的特异性结合更有利(0.272微米颗粒每摩尔SA为0.12摩尔,而2.8微米颗粒每摩尔SA为0.04摩尔)。