Gray C W, Morgan P M, Kane M T
Department of Physiology, University College, Galway, Ireland.
J Reprod Fertil. 1992 Mar;94(2):471-80. doi: 10.1530/jrf.0.0940471.
A factor of low M(r) with growth-promoting effects on rabbit embryos was extracted and purified from commercial bovine serum albumin (BSA). This embryotrophic factor was extracted from BSA dissolved in formic acid by membrane filtration (membrane cutoff of M(r) 10,000) and then freeze-drying of the filtrate. The extract was purified successively by chromatography on G-10 Sephadex, QAE-Sephadex A-25 anion exchange and high-performance liquid chromatography (HPLC) reverse-phase columns. Mass spectrometry of the active reverse-phase material indicated that the major component in this material had an M(r) of 192. The embryotrophic factor in the low M(r) extract of BSA was shown to be citrate, because: (i) the mass spectra of the active reverse-phase material and citrate were identical, (ii) the activity was eluted at the identical position to citrate on an analytical HPLC anion-exchange column, (iii) the original BSA sample was shown by enzyme assay to be heavily contaminated by citrate and (iv) citrate stimulated cell proliferation and expansion of blastocysts.
从商业牛血清白蛋白(BSA)中提取并纯化出一种对兔胚胎具有促生长作用的低分子量因子。该胚胎营养因子是通过膜过滤(截留分子量为10,000)从溶解于甲酸的BSA中提取,然后对滤液进行冷冻干燥而获得。提取物先后通过G - 10葡聚糖凝胶柱色谱、QAE - 葡聚糖凝胶A - 25阴离子交换柱色谱和高效液相色谱(HPLC)反相柱进行纯化。对活性反相物质的质谱分析表明,该物质中的主要成分分子量为192。BSA低分子量提取物中的胚胎营养因子经证实为柠檬酸盐,原因如下:(i)活性反相物质和柠檬酸盐的质谱图相同;(ii)在分析型HPLC阴离子交换柱上,该活性物质与柠檬酸盐在相同位置洗脱;(iii)通过酶法分析表明,原始BSA样品被柠檬酸盐严重污染;(iv)柠檬酸盐可刺激细胞增殖和囊胚扩张。