Vallet L
Dev Biol Stand. 1979;44:3-10.
Gel filtration in Sephadex G200 has been used in the quality control of normal and specific immunoglobulins at the Blood Products Laboratory, Elstree, for more than eleven years. Eluting from a 140 cm column, polymerised and aggregated protein is excluded by the gel, followed in order of elution by fractions containing the IgG dimer and the monomer. After these, smaller protein impurities such as albumin are eluted and then fragments from the proteolytic breakdown of IgG. On a single chromatogram, possibly five distinct peaks may be recorded and their components quantified. Gel filtration in Sephadex G200 provides an alternative to sedimentary boundary ultracentrifugation, by which fragmentation of IgG can be more readily observed. In addition, the fraction containing the polydisperse aggregates excluded by the gel provides an index of adverse treatment of immunoglobulin during preparation and storage.
在埃尔斯特里的血液制品实验室,使用葡聚糖G200进行凝胶过滤来控制正常和特异性免疫球蛋白的质量已超过十一年。从140厘米长的柱子上洗脱时,聚合和聚集的蛋白质被凝胶排除在外,随后按洗脱顺序依次是含有IgG二聚体和单体的组分。在这些之后,较小的蛋白质杂质如白蛋白被洗脱,然后是IgG蛋白水解分解产生的片段。在一张色谱图上,可能会记录到五个不同的峰,并对其成分进行定量。葡聚糖G200凝胶过滤为沉降界面超速离心提供了一种替代方法,通过这种方法可以更容易地观察到IgG的片段化。此外,被凝胶排除的含有多分散聚集体的组分可作为免疫球蛋白在制备和储存过程中受到不良处理的一个指标。