Habener J F, Rosenblatt M, Kemper B, Kronenberg H M, Rich A, Potts J T
Proc Natl Acad Sci U S A. 1978 Jun;75(6):2616-20. doi: 10.1073/pnas.75.6.2616.
The precursor of bovine proparathyroid hormone was synthesized by translation of parathyroid mRNA in a wheat-germ cell-free system. The amino acid sequence of the NH2-terminal extension (the pre sequence) was determined by repetitive Edman degradation of the polypeptide labeled with radioactive amino acids (radiosequencing). The pre sequence of pre-proparathyroid hormone is (formula: see text) which is followed by the sequence of proparathyroid hormone. It is significant that 20 of the 25 amino acids in the sequence are hydrophobic. This high hydrophobicity is consistent with the proposed role of the pre sequence as a membrane-penetrating peptide. The precursor-specific sequence of 31 amino acids was snythesized chemically by the solid-phase technique. This synthetic peptide was shown to bind to the microsomal fraction of homogenates prepared from extracts of parathyroid glands, a finding consistent with the proposed role of the precursor peptide in the attachment of the nascent chain--mRNA--ribosome complex to the endoplasmic reticulum.
牛甲状旁腺激素原的前体是通过在小麦胚芽无细胞系统中翻译甲状旁腺信使核糖核酸(mRNA)合成的。氨基末端延伸部分(前导序列)的氨基酸序列是通过对用放射性氨基酸标记的多肽进行重复的埃德曼降解(放射性测序)来确定的。前甲状旁腺激素原的前导序列为(分子式:见正文),其后是甲状旁腺激素的序列。值得注意的是,该序列中的25个氨基酸中有20个是疏水的。这种高疏水性与前导序列作为膜穿透肽的假定作用一致。通过固相技术化学合成了31个氨基酸的前体特异性序列。该合成肽被证明能与从甲状旁腺提取物制备的匀浆的微粒体部分结合,这一发现与前体肽在新生链-mRNA-核糖体复合物附着于内质网中的假定作用一致。