Tashiro Y, Otsuki E
J Cell Biol. 1970 Jul;46(1):1-16. doi: 10.1083/jcb.46.1.1.
Ultracentrifugal analyses of the native silk proteins extracted from the various parts of the middle silk gland of the mature silkworm have revealed that there exist four components with S degrees (20,w) values of 10S, 9-10S, 9S, and 4S in the extract. It is suggested that the fastest 10S component is the native fibroin synthesized in the posterior silk gland and transferred to the middle silk gland to be stored there, while the slower three components probably correspond to inner, middle, and outer sericins which were synthesized in the posterior, middle, and anterior portion of the middle silk gland, respectively. Native fibroin solution was prepared from the most posterior part of the middle silk gland. Ultracentrifugal analyses have shown that the solution contains considerable amounts of aggregates in addition to the main 10S component. Treatment with lithium bromide (LiBr), urea, or guanidine hydrochloride solution up to 6 M all have failed to dissociate the 10S component. From the sedimentation equilibrium analyses and partial specific volume of 0.71(6), the molecular weight of the 10S component of the native fibroin solution was found to be between 3.2 - 4.2 x 10(5), with a tendency to lie fairly close to 3.7 x 10(5).
对从成熟蚕中部丝腺不同部位提取的天然丝蛋白进行超速离心分析发现,提取物中存在四种组分,其沉降系数(S°(20,w))值分别为10S、9 - 10S、9S和4S。有人提出,最快的10S组分是在后部丝腺中合成并转移至中部丝腺储存的天然丝心蛋白,而较慢的三种组分可能分别对应于在中部丝腺后部、中部和前部合成的内、中、外丝胶蛋白。天然丝心蛋白溶液是从中部丝腺最后端部分制备的。超速离心分析表明,该溶液除主要的10S组分外还含有大量聚集体。用溴化锂(LiBr)、尿素或高达6 M的盐酸胍溶液处理均未能使10S组分解离。通过沉降平衡分析和0.71(6)的偏比容,发现天然丝心蛋白溶液10S组分的分子量在3.2 - 4.2×10⁵之间,且有相当接近3.7×10⁵的趋势。