首页> 外文期刊>Journal of Medicinal Chemistry >Synthesis of mercapto-(+)-methamphetamine haptens and their use for obtaining improved epitope density on (+)-methamphetamine conjugate vaccines
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Synthesis of mercapto-(+)-methamphetamine haptens and their use for obtaining improved epitope density on (+)-methamphetamine conjugate vaccines

机译:巯基-(+)-甲基苯丙胺半抗原的合成及其在(+)-甲基苯丙胺结合物疫苗上获得改善的表位密度的用途

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This study reports the synthesis of the mercapto-hapten (S)-N-(2-(mercaptoethyl)-6-(3-(2-(methylamino)propyl)phenoxy)hexanamide [3, (+)-METH HSMO9] and its use to prepare METH-conjugated vaccines (MCV) from maleimide-activated proteins. MALDI-TOF mass spectrometry analysis of the MCV synthesized using 3 showed there was a high and controllable epitope density on two different carrier proteins. In addition, the MCV produced a substantially greater immunological response in mice than previous METH haptens, and a monoclonal antibody generated from this MCV in mice showed a very high affinity for (+)-METH (K_D = 6.8 nM). The efficient covalent coupling of (+)-METH HSMO9 to the activated carrier proteins suggests that this approach could be cost-effective for large-scale production of MCV. In addition, the general methods described for the synthesis of (+)-METH HSMO9 (3) and its use to synthesize MCV will be applicable for conjugated vaccines of small molecules and other substances of abuse such as morphine, nicotine, and cocaine.
机译:这项研究报告了巯基半抗原(S)-N-(2-(巯基乙基)-6-(3-(2-(甲基(甲基氨基)丙基)苯氧基)己酰胺[3,(+)-METH HSMO9]和MALDI-TOF质谱分析使用3合成的MCV,表明在两种不同的载体蛋白上存在高且可控制的表位密度,此外,MCV还可以通过马来酰亚胺活化的蛋白制备METH偶联疫苗(MCV)。与以前的METH半抗原相比,小鼠的免疫应答明显增强,并且由该MCV产生的单克隆抗体对(+)-METH的亲和力非常高(K_D = 6.8 nM)。 HSMO9与活化的载体蛋白的结合表明该方法对于大规模生产MCV可能具有成本效益,此外,描述了合成(+)-METH HSMO9(3)及其用于合成MCV的一般方法适用于小分子和其他滥用物质的结合疫苗如吗啡,尼古丁和可卡因。

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