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大鼠晶状体囊膜组装的研究。胶原成分的生物合成及部分特性分析。

Studies on the assembly of the rat lens capsule. Biosynthesis and partial characterization of the collagenous components.

作者信息

Heathcote G, Sear C H, Grant M E

出版信息

Biochem J. 1978 Oct 15;176(1):283-94. doi: 10.1042/bj1760283.

Abstract
  1. Isolated rat lens capsules synthesized hydroxy[3H]proline-containing polypeptides when incubated with [3H]proline. 2. The collagenous polypeptides synthesized during a 2 h incubation were analyzed by both gel-filtration chromatography and sodium dodecyl sulphate/polyacrylamide-gel electrophoresis and shown to have an apparent mol.wt. of approx. 180,000. 3. No evidence was obtained for conversion of these polypeptides into a lower-molecular-weight species in experiments where capsules were labelled for 2 h and chased with non-radioactive proline for up to 22 h. However, a time-dependent incorporation of the 180,000-mol.wt. species into a larger collagenous component was observed and this could be prevented by the inclusion of beta-aminopropionitrile in the incubation medium. 4. The radioactive components synthesized by the capsules correspond to subunits of the intact lens capsule and the direct incorporation of the polypeptide of mol.wt. 180,000 into deoxycholate-insoluble basement membrane was demonstrated.
摘要
  1. 分离的大鼠晶状体囊膜与[3H]脯氨酸一起孵育时,能合成含羟[3H]脯氨酸的多肽。2. 通过凝胶过滤色谱法和十二烷基硫酸钠/聚丙烯酰胺凝胶电泳对孵育2小时期间合成的胶原多肽进行分析,结果显示其表观分子量约为180,000。3. 在将囊膜标记2小时并用非放射性脯氨酸追踪长达22小时的实验中,未获得这些多肽转化为低分子量物种的证据。然而,观察到180,000分子量的物种随时间依赖性地掺入到更大的胶原成分中,并且在孵育培养基中加入β-氨基丙腈可防止这种情况发生。4. 囊膜合成的放射性成分对应于完整晶状体囊膜的亚基,并且证明了分子量为180,000的多肽直接掺入到脱氧胆酸盐不溶性基底膜中。

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