Smith John A
University of Alabama at Birmingham, Birmingham, Alabama, USA.
Curr Protoc Mol Biol. 2006 May;Chapter 10:Unit 10.24. doi: 10.1002/0471142727.mb1024s74.
This unit describes a solution-phase radioimmunoassay (RIA) using the double antibody/PEG method. A solution RIA determines the amount of a specific protein (or peptide) in a sample by comparison to a standard curve of the same protein (or peptide). The amount of protein (or peptide) in the sample is determined based on its ability to compete with a radiolabeled tracer for binding to a specific antibody. A secondary antibody and PEG are used to precipitate the primary antibody-protein complexes. The amount of radioactivity in the complex is inversely proportional to the amount of protein in the sample. Under ideal conditions, an RIA is capable of measuring picograms of a protein (or peptide), but only if the tracer is labeled at a high specific activity. To this end, this unit also presents protocols for radioiodination of proteins and peptides using lactoperoxidase or the Bolton-Hunter reagent.
本单元介绍了一种使用双抗体/聚乙二醇(PEG)法的溶液相放射免疫测定(RIA)。溶液相RIA通过与相同蛋白质(或肽)的标准曲线进行比较来确定样品中特定蛋白质(或肽)的量。样品中蛋白质(或肽)的量是根据其与放射性标记示踪剂竞争结合特异性抗体的能力来确定的。使用二抗和PEG沉淀一抗-蛋白质复合物。复合物中的放射性量与样品中蛋白质的量成反比。在理想条件下,RIA能够测量皮克级的蛋白质(或肽),但前提是示踪剂具有高比活性标记。为此,本单元还介绍了使用乳过氧化物酶或博尔顿-亨特试剂对蛋白质和肽进行放射性碘化的方案。