Nagase H, Harris E D, Woessner J F, Brew K
J Biol Chem. 1983 Jun 25;258(12):7481-9.
A proteinase inhibitor which has strong anti-collagenase activity was found in chicken egg white. The inhibitor (pI = 4.9) was purified by poly(ethylene glycol) (5.5-10%) precipitation and chromatography on Ultrogel AcA 34, DEAE-cellulose, and Sephacryl S-300. The final product was homogeneous on 5% polyacrylamide gel electrophoresis. Stoichiometric inhibition was observed with the inhibitor and rabbit synovial collagenase and thermolysin (1:1 molar ratio with thermolysin). The inhibitor ran on sodium dodecyl sulfate-gel electrophoresis with reduction as a single protein band of Mr = 165,000. The molecular weight of the native inhibitor was estimated to be 780,000 by sedimentation equilibrium centrifugation. Centrifugation analysis in 6 M guanidine hydrochloride and of the reduced sample gave M omega = 380,000 and M omega = 195,000, respectively, where M omega is the weight-average molecular weight determined by equilibrium ultra-centrifugation. The results indicated that the inhibitor molecule is a tetramer of identical subunits linked in pairs by disulfide bonds. Since the molecular weight and the quaternary structure of the inhibitor were similar to those of alpha 2-macroglobulin (alpha 2M) in plasma, chicken alpha 2M was isolated and compared with the inhibitor. The inhibitor was not sensitive to methylamine, whereas chicken alpha 2M was. No immunocross-reactivity was observed between the inhibitor and chicken alpha 2M. The NH2-terminal sequence of the egg white inhibitor is Lys-Glu-Pro-Glu-Pro-Gln-Tyr-Val-Leu-Met-Val-Pro-Ala. The sequence of chicken alpha 2M is Ser-Thr-Val-Thr-Glu-Pro-Gln-Tyr-Met-Val-Leu-Leu-Pro-Phe. Considerable homology was found between the two sequences and to the NH2-terminal sequence of human alpha 2M. Monospecific antibody raised against the egg white inhibitor was employed to examine the tissue distribution of the inhibitor. The inhibitor was found only in oviduct and egg white, but not in other tissues or serum of chickens.
在鸡蛋白中发现了一种具有强抗胶原酶活性的蛋白酶抑制剂。该抑制剂(pI = 4.9)通过聚乙二醇(5.5 - 10%)沉淀以及在Ultrogel AcA 34、DEAE - 纤维素和Sephacryl S - 300上的色谱法进行纯化。最终产物在5%聚丙烯酰胺凝胶电泳上呈现均一性。观察到该抑制剂与兔滑膜胶原酶和嗜热菌蛋白酶存在化学计量抑制作用(与嗜热菌蛋白酶的摩尔比为1:1)。该抑制剂在还原条件下进行十二烷基硫酸钠 - 凝胶电泳时呈现为一条Mr = 165,000的单一蛋白带。通过沉降平衡离心法估计天然抑制剂的分子量为780,000。在6 M盐酸胍中对该抑制剂及还原样品进行离心分析,得到的重均分子量Mω分别为380,000和195,000,其中Mω是通过平衡超速离心法测定的重均分子量。结果表明该抑制剂分子是由二硫键成对连接的相同亚基组成的四聚体。由于该抑制剂的分子量和四级结构与血浆中的α2 - 巨球蛋白(α2M)相似,因此分离了鸡α2M并与该抑制剂进行比较。该抑制剂对甲胺不敏感,而鸡α2M对甲胺敏感。在该抑制剂与鸡α2M之间未观察到免疫交叉反应。鸡蛋白抑制剂的NH2 - 末端序列为Lys - Glu - Pro - Glu - Pro - Gln - Tyr - Val - Leu - Met - Val - Pro - Ala。鸡α2M的序列为Ser - Thr - Val - Thr - Glu - Pro - Gln - Tyr - Met - Val - Leu - Leu - Pro - Phe。在这两个序列之间以及与人α2M的NH2 - 末端序列之间发现了相当高的同源性。使用针对鸡蛋白抑制剂产生的单特异性抗体来检测该抑制剂的组织分布。结果发现该抑制剂仅存在于输卵管和鸡蛋白中,而不存在于鸡的其他组织或血清中。