Kirazov L P, Venkov L G, Kirazov E P
Regeneration Research Laboratory, Bulgarian Academy of Sciences, Sofia.
Anal Biochem. 1993 Jan;208(1):44-8. doi: 10.1006/abio.1993.1006.
Although the Bradford protein estimation assay has found wide distribution, it has a number of drawbacks, which in some cases have been shown to produce erroneous results upon comparison to other, more precise, methods for protein estimation. It was found that the underestimation of the protein content of membrane-containing fractions cannot be overcome by pretreatment with NaOH or the detergents employed (Triton X-100, sodium dodecyl sulfate, 3[(3-cholamidopropyl)-dimethylammonio]propanesulfonic acid) and the protein estimates obtained do not agree with estimates obtained by the Lowry assay. Upon storage of fractions at -20 degrees C there is a considerable loss of dye binding activity, varying in accordance with the membrane content of the fractions, reaching up to 58% in the case of membrane-enriched fractions stored at -20 degrees C for 15 days. Pretreatment with the employed agents brought about an equal increase of dye binding capacity, specific for the individual fractions; however, none of these agents could recover the dye binding activity lost during several days of storage at -20 degrees C. It is suggested that the straightforward Bradford procedure has a rather limited scope of application, particularly concerning membrane-containing samples, and requires preliminary studies to determine its applicability according to the nature of the biological material examined.
尽管 Bradford 蛋白质定量测定法已得到广泛应用,但它存在一些缺点,在某些情况下,与其他更精确的蛋白质定量方法相比,已证明会产生错误结果。研究发现,用 NaOH 或所用的洗涤剂(Triton X-100、十二烷基硫酸钠、3-[(3-胆酰胺丙基)-二甲基铵基]丙烷磺酸)进行预处理无法克服对含膜组分蛋白质含量的低估,并且所获得的蛋白质定量结果与 Lowry 测定法得到的结果不一致。当组分在 -20℃储存时,染料结合活性会有相当大的损失,这根据组分的膜含量而有所不同,对于在 -20℃储存 15 天的富含膜的组分,损失高达 58%。用所用试剂进行预处理会使各组分特有的染料结合能力同等增加;然而,这些试剂都无法恢复在 -20℃储存数天期间损失的染料结合活性。建议直接的 Bradford 方法应用范围相当有限,特别是对于含膜样品,并且需要进行初步研究以根据所检测生物材料的性质确定其适用性。