Jauhiainen M, Laitinen M, Marniemi J, Liippo K, Penttilä I, Hietanen E
Clin Chem. 1983 Oct;29(10):1731-5.
A chromatofocusing column method for isolating ApoB is described. LDL is first isolated by sequential ultracentrifugation and delipidated with n-butanol/diisopropyl ether. Chromatofocusing of ApoLDL yielded a large ApoB peak at pI 5.0-5.3. ApoA-I and ApoC-II were prepared analogously, with HDL and VLDL as the source of apoprotein. Antisera were raised in rabbits, and electroimmunoassay techniques were used for determination. ApoB was water-soluble after chromatofocusing. Intra-assay precision (CV) was 4.7% for ApoA-I, 7.8% for ApoB in the "rocket" electrophoresis. Interassay precision (CV) was 6% for ApoA-I and 8% for ApoB. Apolipoprotein concentrations were measured in subjects who had undergone lung resection and patients with obstructive pulmonary disease. After lung resection, the concentration of ApoA-I in serum was significantly decreased (p less than 0.001) and that of ApoB significantly increased (p less than 0.001) as compared with controls. The ApoA-I/ApoB ratio was significantly lower in the lung-resection group. ApoA-I and ApoB concentrations were unchanged in chronic obstructive pulmonary disease. ApoC-II concentrations in each group were similar to those for control subjects. Of the lipids, values for total cholesterol were above normal after lung resection (p less than 0.002), as were those for triglycerides (p less than 0.02).
描述了一种用于分离载脂蛋白B(ApoB)的色谱聚焦柱方法。首先通过连续超速离心分离低密度脂蛋白(LDL),并用正丁醇/二异丙醚脱脂。对载脂蛋白LDL(ApoLDL)进行色谱聚焦,在pH值5.0 - 5.3处产生一个大的ApoB峰。载脂蛋白A - I(ApoA - I)和载脂蛋白C - II(ApoC - II)以类似方法制备,分别以高密度脂蛋白(HDL)和极低密度脂蛋白(VLDL)作为载脂蛋白来源。在兔体内制备抗血清,并采用电免疫测定技术进行检测。色谱聚焦后ApoB可溶于水。在“火箭”电泳中,ApoA - I的批内精密度(CV)为4.7%,ApoB为7.8%。ApoA - I的批间精密度(CV)为6%,ApoB为8%。对接受肺切除术的患者和阻塞性肺疾病患者测定了载脂蛋白浓度。肺切除术后,与对照组相比,血清中ApoA - I浓度显著降低(p < 0.001),ApoB浓度显著升高(p < 0.001)。肺切除组的ApoA - I/ApoB比值显著降低。慢性阻塞性肺疾病患者的ApoA - I和ApoB浓度无变化。每组的ApoC - II浓度与对照组相似。在脂质方面,肺切除术后总胆固醇值高于正常(p < 0.002),甘油三酯值也高于正常(p < 0.02)。