Sherwin A L, Karpati G, Bulcke J A
Proc Natl Acad Sci U S A. 1969 Sep;64(1):171-5. doi: 10.1073/pnas.64.1.171.
A specific antiserum against skeletal muscle creatine phosphokinase has been obtained by immunizing chickens with purified rabbit skeletal muscle creatine phosphokinase. The antiserum was organ- rather than species-specific and reacted equally well with creatine phosphokinase from rabbit, guinea pig, and human skeletal muscle. Immunological specificity was verified by double immunodiffusion in agar gel where the precipitin line exhibited creatine phosphokinase activity. In solution the antiserum inhibited the enzymatic activity of creatine phosphokinase. By means of the immunofluorescent technique, creatine phosphokinase was localized in the intermyofibrillar space of normal human skeletal muscle fibers in cryostat sections. A higher concentration of the enzyme was found in fibers which have primarily an anaerobic enzyme profile (type II fibers) as determined by conventional histochemical reactions.
通过用纯化的兔骨骼肌肌酸磷酸激酶免疫鸡,获得了一种针对骨骼肌肌酸磷酸激酶的特异性抗血清。该抗血清具有器官特异性而非物种特异性,与兔、豚鼠和人骨骼肌中的肌酸磷酸激酶反应同样良好。通过琼脂凝胶双免疫扩散验证了免疫特异性,其中沉淀线表现出肌酸磷酸激酶活性。在溶液中,抗血清抑制了肌酸磷酸激酶的酶活性。借助免疫荧光技术,在恒冷箱切片中,肌酸磷酸激酶定位于正常人骨骼肌纤维的肌原纤维间间隙。通过传统组织化学反应确定,在主要具有无氧酶谱的纤维(II型纤维)中发现了较高浓度的该酶。