Cole W C, Leblanc A D, Jhingran S G
Baylor College of Medicine, Department of Medicine, Houston, TX 77030.
Int J Rad Appl Instrum B. 1988;15(2):177-9. doi: 10.1016/0883-2897(88)90085-2.
Current methods of 111In chelate conjugation labeling of antibodies expose the protein to pH 5-6 during 111In chelation. These conditions could be detrimental if the antibody is acid labile. We have successfully labeled human IgG via the cyclic anhydride of DPTA and 111In-oxyquinoline(oxine). Chelation was achieved at pH 6.9-8.4 and was complete within 1 min at room temperature. The chelation was sensitive to trace metal contamination on labware and in some reagents (including commercial 111In-oxine).
目前用于抗体的铟 - 111螯合物结合标记的方法在铟 - 111螯合过程中将蛋白质暴露于pH 5 - 6的环境中。如果抗体对酸不稳定,这些条件可能是有害的。我们已经通过二乙三胺五乙酸(DPTA)的环酐和111In - 喹啉(喹啉醇)成功地标记了人免疫球蛋白G(IgG)。在pH 6.9 - 8.4下实现螯合,并且在室温下1分钟内完成。螯合对实验室器具和某些试剂(包括市售的111In - 喹啉醇)中的痕量金属污染敏感。