Matthews I, Mata A M, Lee A G, East J M
SERC Centre for Molecular Recognition, University of Southampton, UK.
Biochim Biophys Acta. 1993 Mar 14;1146(2):265-74. doi: 10.1016/0005-2736(93)90365-7.
The 53 kDa glycoprotein from sarcoplasmic reticulum was shown to be protected from proteolysis by trypsin, V8 proteinase and proteinase K in intact vesicles yet readily digested in the presence of the non-denaturing detergent C12E8. Competitive ELISAs with a library of seven monoclonal antibodies raised against the 53 kDa glycoprotein showed that the epitopes for these antibodies were only accessible in C12E8 solubilised and not intact sarcoplasmic reticulum. When the monoclonal antibodies against the 53 kDa glycoprotein were assessed for their effect on the uptake of Ca2+ by sarcoplasmic reticulum no effect was detected; neither were these antibodies able to augment the inhibitory influences of anti-(Ca(2+)-Mg2+)-ATPase monoclonal antibodies on Ca2+ uptake. These data indicate that the 53 kDa glycoprotein is located in the lumen of the sarcoplasmic reticulum.
肌浆网中的53 kDa糖蛋白在完整囊泡中可免受胰蛋白酶、V8蛋白酶和蛋白酶K的蛋白水解作用,但在非变性去污剂C12E8存在时则易于被消化。用针对53 kDa糖蛋白产生的七种单克隆抗体文库进行的竞争性ELISA表明,这些抗体的表位仅在C12E8溶解的而非完整的肌浆网中可及。当评估针对53 kDa糖蛋白的单克隆抗体对肌浆网摄取Ca2+的影响时,未检测到作用;这些抗体也无法增强抗(Ca(2+)-Mg2+)-ATP酶单克隆抗体对Ca2+摄取的抑制作用。这些数据表明,53 kDa糖蛋白位于肌浆网腔中。