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Biosynthesis and processing of placental alkaline phosphatase.

作者信息

Ito F, Chou J Y

出版信息

Biochem Biophys Res Commun. 1983 Mar 16;111(2):611-8. doi: 10.1016/0006-291x(83)90350-9.

DOI:10.1016/0006-291x(83)90350-9
PMID:6838575
Abstract

Polypeptides of 61,500 and 64,500 apparent molecular weights were the precursor and fully processed forms of placental alkaline phosphatase monomer synthesized by choriocarcinoma cells in vivo. [3H] Mannose was incorporated into both polypeptides whereas [3H] glucosamine was incorporated mainly into the 64,500-dalton polypeptide, suggesting processing by the addition of glucosamine moieties. In the absence of microsomal membranes, choriocarcinoma mRNA directed the cell-free synthesis of the preprotein form of alkaline phosphatase monomer of apparent Mr = 60,000. The unglycosylated monomer had an apparent Mr = 58,000. In the presence of microsomal membranes, the 60,000-dalton polypeptide was processed to a polypeptide of apparent Mr = 61,500, comigrating with the precursor form of alkaline phosphatase monomer.

摘要

相似文献

1
Biosynthesis and processing of placental alkaline phosphatase.
Biochem Biophys Res Commun. 1983 Mar 16;111(2):611-8. doi: 10.1016/0006-291x(83)90350-9.
2
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引用本文的文献

1
Expression of different-sized placental alkaline phosphatase mRNAs in placenta and choriocarcinoma cells.不同大小胎盘碱性磷酸酶mRNA在胎盘和绒毛膜癌细胞中的表达。
Proc Natl Acad Sci U S A. 1986 Jun;83(11):3781-5. doi: 10.1073/pnas.83.11.3781.
2
Cloning, sequencing, and chromosomal localization of human term placental alkaline phosphatase cDNA.人足月胎盘碱性磷酸酶cDNA的克隆、测序及染色体定位
Proc Natl Acad Sci U S A. 1985 Dec;82(24):8715-9. doi: 10.1073/pnas.82.24.8715.