Smal M A, Baldo B A, Redmond J W
Kolling Institute of Medical Research, Royal North Shore Hospital, St. Leonards, N.S.W., Australia.
Lipids. 1991 Dec;26(12):1130-5. doi: 10.1007/BF02536516.
Platelet activating factor (PAF), a naturally occurring phospholipid with many potent physiological and pharmacological activities, is implicated as a mediator of many diseases. An immunoassay for PAF would greatly improve quantitation, and hence PAF-specific antibodies were required. Chemically-reactive analogs of PAF, containing an aldehyde group at the end of the 1-O-alkyl chain (hexyl or dodecyl), were synthesized from readily available materials. During the multi-step synthetic procedure, the aldehyde group was protected as an acetal, which was converted by mild acidic hydrolysis to the aldehyde immediately prior to protein coupling. These analogs were coupled to methylated bovine serum albumin and the resultant conjugates were injected into rabbits. Antibodies to PAF were detected using a solid phase radioimmunoassay based on Protein A-Sepharose. The dodecyl PAF conjugate proved to be the more immunogenic conjugate with more than half of the rabbits producing significant levels of antibodies (at least a 10-fold increase in radioactive uptake over pre-immune levels). Results from solid phase immunoassays employing nitrocellulose discs impregnated with PAF, lysoPAF, lecithin, lysolecithin and 2-O-methyl-lysoPAF indicated that the antibodies recognized only PAF. PAF-specific antibodies were isolated by affinity chromatography using a column of PAF-poly(lysine) conjugated to carboxy-activated polyacrylamide. The antibodies may be employed in a sensitive and specific immunoassay for PAF and for many other studies involving PAF.
血小板活化因子(PAF)是一种具有多种强大生理和药理活性的天然磷脂,被认为是多种疾病的介质。PAF免疫测定法将极大地改善定量分析,因此需要PAF特异性抗体。从易得的原料合成了PAF的化学反应类似物,其在1-O-烷基链(己基或十二烷基)末端含有醛基。在多步合成过程中,醛基被保护为缩醛,在与蛋白质偶联之前,通过温和的酸性水解立即将其转化为醛。这些类似物与甲基化牛血清白蛋白偶联,并将所得结合物注射到兔子体内。使用基于蛋白A-琼脂糖的固相放射免疫测定法检测PAF抗体。结果表明,十二烷基PAF结合物具有更强的免疫原性,超过半数的兔子产生了高水平的抗体(放射性摄取比免疫前水平至少增加10倍)。采用浸渍有PAF、溶血PAF、卵磷脂、溶血卵磷脂和2-O-甲基溶血PAF的硝酸纤维素圆盘进行的固相免疫测定结果表明,这些抗体仅识别PAF。通过使用与羧基活化聚丙烯酰胺偶联的PAF-聚(赖氨酸)柱进行亲和层析,分离出PAF特异性抗体。这些抗体可用于PAF的灵敏特异性免疫测定以及许多其他涉及PAF的研究。