Suda K, Barde Y A, Thoenen H
Proc Natl Acad Sci U S A. 1978 Aug;75(8):4042-6. doi: 10.1073/pnas.75.8.4042.
High levels of nerve growth factor (NGF) determined by competition radioimmunoassay do not agree with values obtained by bioassay. This discrepancy is illustrated here with rat and mouse serum as examples in which values up to 1000 ng/ml have been found by using competition radioimmunoassays. An explanation for the discordant results is presented: serum components bind NGF with an intermediate affinity (Kd = 10(-7) M) but with a very large capacity (up to 0.5 mg of NGF per ml of rat serum). The binding of 125I-labeled NGF to serum components competes with the binding to the solid-phase antibodies (Kd = 10(-9)M) present in limiting amounts, according to the principle of competition radioimmunoassays. Thus, less radioactivity is recovered bound to the antibodies and this gives the erroneous impression that NGF is present. To overcome this difficulty, a two-site radioimmunoassay has been developed which utilizes nonlimiting numbers of antibody binding sites. This assay provides a reliable determination of NGF levels in serum and it can be shown that in rat and mouse serum (either sex) there is less than 5 ng of NGF per ml, in agreement with the results of the bioassay.
通过竞争放射免疫测定法测定的高水平神经生长因子(NGF)与生物测定法得到的值不一致。本文以大鼠和小鼠血清为例说明了这种差异,在使用竞争放射免疫测定法时,已发现其值高达1000 ng/ml。文中给出了结果不一致的解释:血清成分以中等亲和力(Kd = 10^(-7) M)结合NGF,但结合能力非常大(每毫升大鼠血清高达0.5 mg NGF)。根据竞争放射免疫测定法的原理,125I标记的NGF与血清成分的结合与与限量存在的固相抗体(Kd = 10^(-9)M)的结合相互竞争。因此,与抗体结合回收的放射性较少,这就产生了NGF存在的错误印象。为克服这一困难,已开发出一种双位点放射免疫测定法,该方法利用了非限量的抗体结合位点。该测定法可可靠地测定血清中的NGF水平,结果表明,大鼠和小鼠血清(无论雌雄)中每毫升NGF含量均低于5 ng,这与生物测定法的结果一致。