Shimura K, Kasai K
Faculty of Pharmaceutical Sciences, Teikyo University, Kanagawa, Japan.
Electrophoresis. 1995 Aug;16(8):1479-84. doi: 10.1002/elps.11501601245.
Commercially available peptides, mostly angiotensin derivatives, were labeled at their N-terminal amino group with 5-carboxytetramethylrhodamine succinimidyl ester, to obtain fluorescent pI markers for capillary isoelectric focusing with fluorescence detection. The labeled peptides were purified by reversed-phase chromatography. They were well separated on isoelectric focusing in a polyacrylamide gel slab and their pIs were determined by comigration with protein-pI markers. The fluorescent markers could be detected as sharp peaks in capillary isoelectric focusing with laser-induced fluorescence detection (He-Ne laser, 1 mW, 543.5 nm). The detection limit was found to be around 3 x 10(-12) M (0.8 amol). Tetramethylrhodamine-labeled pea lectin (3 pg) was subjected to capillary isoelectric focusing and the pIs of the fluorescent derivatives of the lectin were determined by using the fluorescence-labeled peptides as pI markers.
市售肽(大多为血管紧张素衍生物)在其N端氨基用5-羧基四甲基罗丹明琥珀酰亚胺酯进行标记,以获得用于毛细管等电聚焦荧光检测的荧光pI标记物。标记后的肽通过反相色谱法进行纯化。它们在聚丙烯酰胺凝胶板上进行等电聚焦时能很好地分离,其pI通过与蛋白质pI标记物共迁移来确定。在毛细管等电聚焦中,利用激光诱导荧光检测(氦氖激光,1 mW,543.5 nm)可将荧光标记物检测为尖锐峰。检测限约为3×10⁻¹² M(0.8 amol)。将四甲基罗丹明标记的豌豆凝集素(3 pg)进行毛细管等电聚焦,并以荧光标记肽作为pI标记物来确定凝集素荧光衍生物的pI。