Giorgi F, Cecchettini A, Locci M T, Masetti M, Peccatori M
Department of Biomedicine, University of Pisa, Italy.
Arch Insect Biochem Physiol. 1997;36(4):335-48. doi: 10.1002/(SICI)1520-6327(1997)36:4<335::AID-ARCH6>3.0.CO;2-Q.
Vitellins from ovarian follicles and newly laid eggs of the stick insect Carausius morosus were examined by ion exchange chromatography on a HPLC Mono Q column. Under these conditions, vitellins from newly laid eggs resolved as two distinct peaks, referred to as VtA and VtB, that eluted at 8.5 and 12.0 min, respectively. On native gels, both VtA and VtB separated into two different variant forms (VtA' and VtA", VtB' and VtB"). By two-dimensional gel electrophoresis, VtA' and VtA" were shown to contain polypeptides A1, A2 and A3. On the other hand, VtB' and VtB" appeared to comprise polypeptides B1 and B2 and B1, A1, A2, B2 and A3*, respectively. A similar Vt polypeptide composition was also observed by size-exclusion chromatography of vitellins from newly laid eggs. Vitellins from early vitellogenic ovarian follicles resolved into a single chromatographic peak at 7.5 min that coeluted with a major peak from the hemolymph of egg-laying females. Ovarian follicles progressively more advanced in development exhibited a more complex chromatographic profile, consisting of three separate peaks. By two-dimensional gel immunoelectrophoresis, vitellins from ovarian follicles appeared to consist of two closely related, immunologically cross-reacting antigens that gradually shifted apart as ovarian development proceeded to completion. By size-exclusion chromatography, each Vt from ovarian follicles was shown to consist of a unique set of polypeptides different from those listed above. Single ovarian follicles were fractionated into yolk granules and yolk fluid ooplasm and tested by immunoblotting against Mab 12. Under these conditions, VtA variant forms in yolk granules and yolk fluid ooplasm reacted differently. Sections from ovarian follicles in different developmental stages were exposed to Mab 12 and stained with a peroxidase-conjugated, goat anti-mouse antibody. Regardless of the developmental stage attained, staining for peroxidase was restricted to free yolk granules, suggesting that native vitellins in stick insects are structurally modified upon fusion into the yolk fluid ooplasm.
利用高效液相色谱法(HPLC)的Mono Q柱,通过离子交换色谱法对竹节虫墨胸竹节虫(Carausius morosus)卵巢卵泡和新产卵中的卵黄蛋白进行了检测。在这些条件下,新产卵中的卵黄蛋白分离为两个不同的峰,分别称为VtA和VtB,它们分别在8.5分钟和12.0分钟洗脱。在天然凝胶上,VtA和VtB均分离为两种不同的变体形式(VtA'和VtA",VtB'和VtB")。通过二维凝胶电泳显示,VtA'和VtA"含有多肽A1、A2和A3。另一方面,VtB'和VtB"似乎分别包含多肽B1和B2以及B1、A1、A2、B2和A3*。通过对新产卵中的卵黄蛋白进行尺寸排阻色谱分析,也观察到了类似的Vt多肽组成。早期卵黄发生卵巢卵泡中的卵黄蛋白在7.5分钟时分离为一个单一的色谱峰,该峰与产卵雌性血淋巴中的一个主峰共洗脱。发育程度逐渐更高的卵巢卵泡呈现出更复杂的色谱图谱,由三个单独的峰组成。通过二维凝胶免疫电泳,卵巢卵泡中的卵黄蛋白似乎由两种密切相关、免疫交叉反应的抗原组成,随着卵巢发育的完成,它们逐渐分开。通过尺寸排阻色谱分析表明,卵巢卵泡中的每个Vt由一组不同于上述的独特多肽组成。将单个卵巢卵泡分离为卵黄颗粒和卵黄液卵质,并针对单克隆抗体12进行免疫印迹检测。在这些条件下,卵黄颗粒和卵黄液卵质中的VtA变体形式反应不同。将不同发育阶段的卵巢卵泡切片用单克隆抗体12处理,并用过氧化物酶偶联的山羊抗小鼠抗体染色。无论达到何种发育阶段,过氧化物酶染色都局限于游离的卵黄颗粒,这表明竹节虫中的天然卵黄蛋白在融合到卵黄液卵质中时会发生结构修饰。