Smith J A, Ham J, Winslow D P, O'Hare M J, Rudland P S
J Chromatogr. 1984 Feb 10;305(2):295-308. doi: 10.1016/s0378-4347(00)83344-7.
Various epidermal growth factor preparations obtained from the mouse submaxillary gland (mEGF), have been separated into a number of components by reversed-phase high-performance liquid chromatography (HPLC). It is shown here, however, that when the mEGF is isolated rapidly, using only reversed-phase HPLC for trace enrichment and high-resolution fractionation, it is a single molecular species as determined with several ion-pairing solvent systems, provided that proteolysis is inhibited in the original extracts. This indicates that the minor components of mEGF that have been reported are artefacts formed during the isolation procedure, and are of no biological significance. The products of deliberate mild degradation of mEGF are shown to produce similar chromatographic profiles to those observed in samples of mEGF prepared in the absence of proteolytic inhibitors. Rat EGF has been isolated in a similar manner, and is shown to share many of the properties of the major tryptic digestion product of mEGF.
从小鼠颌下腺获得的各种表皮生长因子制剂(mEGF),已通过反相高效液相色谱(HPLC)分离成多个组分。然而,本文表明,当仅使用反相HPLC进行痕量富集和高分辨率分级分离来快速分离mEGF时,在几种离子对溶剂系统测定下它是单一分子种类,前提是在原始提取物中抑制蛋白水解。这表明已报道的mEGF的次要组分是在分离过程中形成的假象,并无生物学意义。mEGF经刻意温和降解产生的产物,其色谱图与在无蛋白水解抑制剂情况下制备的mEGF样品中观察到的相似。大鼠表皮生长因子(EGF)已以类似方式分离出来,并显示出与mEGF主要胰蛋白酶消化产物的许多特性相同。