Mikuni-Takagaki Y, Glimcher M J
Laboratory for the Study of Skeletal Disorders and Rehabilitation, Harvard Medical School, Children's Hospital, Boston, MA 02115.
Biochem J. 1990 Jun 15;268(3):585-91. doi: 10.1042/bj2680585.
In order to understand the mechanism of the post-translational processing of bone phosphoproteins in embryonic bone, periosteal bone strips isolated from 12-day-embryonic-chick tibiae were cultured and the bone proteins labelled with Na2H32PO4. Of the total radiolabelled proteins recovered from the medium and bone extracts in the absence of SDS ('medium', 'EDTA extract' and 'EDTA/guanidinium chloride extract'), nearly 80% of the radioactivity was found in the EDTA extract. The three major radiolabelled phosphoproteins in the EDTA extract of apparent Mr 68,000, 63,000 and 58,000 reacted with polyclonal as well as monoclonal antibodies raised against '32-kDa' and '150-kDa' bone phosphoproteins which were derived from 14-week-old chicken. Therefore these phosphorylated embryonic proteins are identified as chicken bone phosphoproteins. Judging from their common N-terminal sequences, differences in the patterns obtained by labelling them with several radioisotopes, and slightly different amino acid compositions, these components seem to have been derived from the same original protein by sequential proteolytic cleavage and other processing such as glycosylation and phosphorylation.
为了解胚胎骨中骨磷蛋白的翻译后加工机制,从12日龄鸡胚胫骨分离出骨膜骨条进行培养,并用Na2H32PO4标记骨蛋白。在不含十二烷基硫酸钠(SDS)的情况下,从培养基和骨提取物中回收的总放射性标记蛋白(“培养基”、“乙二胺四乙酸(EDTA)提取物”和“EDTA/氯化胍提取物”)中,近80%的放射性存在于EDTA提取物中。EDTA提取物中表观分子量为68,000、63,000和58,000的三种主要放射性标记磷蛋白,与针对源自14周龄鸡的“32 kDa”和“150 kDa”骨磷蛋白产生的多克隆抗体以及单克隆抗体发生反应。因此,这些磷酸化的胚胎蛋白被鉴定为鸡骨磷蛋白。从它们共同的N端序列、用几种放射性同位素标记获得的模式差异以及略有不同的氨基酸组成来看,这些成分似乎是通过连续的蛋白水解切割以及糖基化和磷酸化等其他加工过程,从同一原始蛋白衍生而来。