Dzau V J, Tanaka A, Pratt R E
Clin Exp Hypertens A. 1982;4(11-12):1973-85. doi: 10.3109/10641968209062363.
The biosynthesis of renin in the mouse submaxillary gland was defined using both cell-free translation and pulse-labelling methods. Renin is synthesized as a preproform and cleaved by microsomes to the proform. Prorenin (MW = 46 kilodaltons, pI 6.35) is processed intracellulary into an intermediate form (MW = 41 kilodaltons). The latter is converted by a slow intracellular process to the final major storage form (MW = 37 kilodaltons). Both the intermediate and the 37 KD forms are secreted. The biosynthetic precursor does not bind to pepstatin-aminohexyl sepharose. In parallel experiments, using rapid tissue extraction with buffers containing protease inhibitors and fractionation with affinity chromatography, we have also identified in the mouse submaxillary gland an inactive form of renin which has a MW of 48 2 KD and pI of 6.4. Mouse submaxillary gland inactive renin binds to affigel-blue and not to pepstatin-sepharose. The similarity in the properties of inactive renin and the biosynthetic renin precursor lends further support to the suggestion that tissue inactive renin may be the renin precursor.
利用无细胞翻译和脉冲标记方法确定了小鼠颌下腺中肾素的生物合成过程。肾素以前体形式合成,并被微粒体切割成前体形式。肾素原(分子量=46千道尔顿,等电点6.35)在细胞内加工成中间形式(分子量=41千道尔顿)。后者通过缓慢的细胞内过程转化为最终的主要储存形式(分子量=37千道尔顿)。中间形式和37千道尔顿形式都会分泌。生物合成前体不与胃蛋白酶抑制剂 - 氨基己基琼脂糖结合。在平行实验中,使用含有蛋白酶抑制剂的缓冲液进行快速组织提取并通过亲和色谱进行分级分离,我们还在小鼠颌下腺中鉴定出一种无活性的肾素形式,其分子量为48.2千道尔顿,等电点为6.4。小鼠颌下腺无活性肾素与Affigel - blue结合,而不与胃蛋白酶抑制剂 - 琼脂糖结合。无活性肾素和生物合成肾素前体特性的相似性进一步支持了组织无活性肾素可能是肾素前体的观点。