ADP RIBOSYL CYCLASE ACTIVITY OF A NOVEL BONE-MARROW STROMAL CELL-SURFACE MOLECULE, BST-1

ADP RIBOSYL CYCLASE ACTIVITY OF A NOVEL BONE-MARROW STROMAL CELL-SURFACE MOLECULE, BST-1
复制标题

DOI:
10.1016/0014-5793(94)01279-2
复制
发表时间:
1994-12-19
期刊:
影响因子:
3.5
通讯作者:
HIRANO, T
HIRANO, T
中科院分区:
生物学3区
文献类型:
--
作者:
HIRATA, Y;KIMURA, N;HIRANO, T

文献摘要

被引文献

相似文献

人BST-1是一种骨髓基质细胞表面分子,是一种促进前B细胞生长的GPI锚定蛋白。推导的人和小鼠BST-1的氨基酸序列与CD 38和Astrasia ADP核糖基环化酶的氨基酸序列有30%左右的同源性。因此,BST-1可能与CD 38一样具有ADP核糖基环化酶活性。在这里,我们报告建立一个稳定的CHO细胞系,它分泌截短的人可溶性BST-1,并显示纯化的可溶性BST-1显示ADP核糖环化酶和cADPR水解酶活性。
Human BST-1, a bone marrow stromal cell surface molecule, is a GPI-anchored protein that facilitates the growth of pre-B cells. The deduced amino acid sequences of human and mouse BST-1 show around 30% homology with those of CD38 and Aplysia ADP ribosyl cyclase. Therefore, like CD38, BST-1 might possess ADP ribosyl cyclase activity. Here, we report the establishment of a stable transformant CHO cell line, which secretes truncated human soluble BST-1, and show that purified soluble BST-1 displays both ADP ribosyl cyclase and cADPR hydrolase activities.