Houen G, Jakobsen M H, Svaerke C, Koch C, Barkholt V
Department of Autoimmunology, Statens Serum Institut, Copenhagen, Denmark.
J Immunol Methods. 1997 Aug 7;206(1-2):125-34. doi: 10.1016/s0022-1759(97)00097-5.
A solid phase conjugation method is described based on the preadsorption of proteins to aluminium hydroxide adjuvant followed by activation of the adsorbed carrier proteins with iodoacetic acid N-hydroxysuccinimidester or other conjugation reagents. Cysteine-containing peptides were coupled to the iodoacetic acid-activated carrier-adjuvant particles through their SH groups. No dialysis is required since the reaction product is isolated at each step of the procedure by a simple centrifugation and can easily be extensively washed between individual manipulations. The method generates peptide-carrier-adjuvant particles with sterically defined presentation of the peptides at the surface of the particles. When used for immunization of mice and rabbits the conjugates elicited high-titered specific anti-peptide sera, which reacted well with the parent protein in ELISA. The strongest reactions were with the denatured form of the parent protein. On immunoblots antisera to the N- and C-terminus of calreticulin recognized the same M, 52,000 protein.
描述了一种固相偶联方法,该方法基于蛋白质预先吸附到氢氧化铝佐剂上,然后用碘乙酸N-羟基琥珀酰亚胺酯或其他偶联试剂激活吸附的载体蛋白。含半胱氨酸的肽通过其SH基团与碘乙酸活化的载体-佐剂颗粒偶联。由于在该程序的每个步骤中通过简单的离心分离反应产物,并且在各个操作之间可以很容易地进行广泛洗涤,因此不需要透析。该方法产生肽-载体-佐剂颗粒,肽在颗粒表面具有空间定义的呈现。当用于免疫小鼠和兔子时,偶联物引发了高滴度的特异性抗肽血清,其在ELISA中与亲本蛋白反应良好。最强的反应是与亲本蛋白的变性形式。在免疫印迹上,针对钙网蛋白N端和C端的抗血清识别相同的52,000 M蛋白。