Kanai Y, Miura K, Uehara T, Amagai M, Takeda O, Tanuma S, Kurosawa Y
Department of Molecular Oncology, University of Tokyo, Japan.
Biochem Biophys Res Commun. 1993 Oct 29;196(2):729-36. doi: 10.1006/bbrc.1993.2310.
We previously established a clone of cells termed KML1-7 which produces a soluble factor that boosts anti-DNA antibody production both in vitro and in vivo across the H-2 barrier. By using the purified protein, termed nucleobindin (Nuc), we cloned cDNA and produced recombinant(r) Nuc in E.coli. Although the purified rNuc showed biological activities such as anti-DNA antibody boosting and DNA binding, there was no evidence that Nuc is really associated with autoimmune status in lupus-prone MRL/lpr mice. Here we report that identification of Nuc was successful from the sera of MRL/lpr mice, but not from those of the substrain MRL/n mice, which show no apparent autoimmune syndrome at the same age of MRL/lpr mice, by means of immunochemical as well as N-terminal amino-acid sequencing methods.
我们之前建立了一个名为KML1-7的细胞克隆,该克隆产生一种可溶性因子,可在体外和体内跨越H-2屏障促进抗DNA抗体的产生。通过使用纯化的蛋白质,即核结合蛋白(Nuc),我们克隆了cDNA并在大肠杆菌中产生了重组(r)Nuc。尽管纯化的rNuc表现出抗DNA抗体增强和DNA结合等生物学活性,但没有证据表明Nuc与易患狼疮的MRL/lpr小鼠的自身免疫状态真正相关。在此我们报告,通过免疫化学以及N端氨基酸测序方法,成功从MRL/lpr小鼠的血清中鉴定出Nuc,但未从同年龄的MRL/lpr小鼠未表现出明显自身免疫综合征的亚系MRL/n小鼠的血清中鉴定出Nuc。