Vaidyanathan Ganesan, Zalutsky Michael R
Department of Radiology, Duke University Medical Center, Durham, North Carolina, USA.
Nat Protoc. 2007;2(2):282-6. doi: 10.1038/nprot.2007.20.
This protocol describes a detailed procedure for the synthesis of N-succinimidyl 4-guanidinomethyl-3-[*I]iodobenzoate ([*I]SGMIB), an agent useful in the radio-iodination of proteins, including monoclonal Abs, and peptides that undergo internalization after receptor or antigen binding. In this procedure, the tin precursor N-succinimidyl 4-[N1,N2-bis(tert-butyloxycarbonyl)guanidinomethyl]-3-(trimethylstannyl)benzoate (Boc-SGMTB, 3) was first radio-iodinated to [*I]Boc-SGMIB, a derivative of [*I]SGMIB with the guanidine function protected with Boc groups. Treatment of [*I]Boc-SGMIB with trifluoroacetic acid delivered the final product. The total time for the synthesis and purification of [*I]Boc-SGMIB and its subsequent de-protection is approximately 140 min.
本方案描述了用于合成N-琥珀酰亚胺基4-胍基甲基-3-[*I]碘苯甲酸酯([*I]SGMIB)的详细步骤,该试剂可用于蛋白质(包括单克隆抗体)以及在受体或抗原结合后发生内化的肽的放射性碘化。在此过程中,首先将锡前体N-琥珀酰亚胺基4-[N1,N2-双(叔丁氧羰基)胍基甲基]-3-(三甲基锡基)苯甲酸酯(Boc-SGMTB,3)放射性碘化生成[*I]Boc-SGMIB,它是[*I]SGMIB的一种衍生物,其胍基功能被Boc基团保护。用三氟乙酸处理[*I]Boc-SGMIB即可得到最终产物。[*I]Boc-SGMIB的合成、纯化及其后续脱保护的总时间约为140分钟。