Na D H, Park M O, Choi S Y, Kim Y S, Lee S S, Yoo S D, Lee H S, Lee K C
Drug Targeting Laboratory, College of Pharmacy, SungKyunKwan University, Suwon, South Korea.
J Chromatogr B Biomed Sci Appl. 2001 Apr 15;754(1):259-63. doi: 10.1016/s0378-4347(00)00599-5.
A capillary electrophoretic method (CE) was developed for the determination of the PEG-modification sites of three positional isomers of mono-PEG modified salmon calcitonins (mono-PEG-sCTs). Resistance to proteolytic degradation on the PEG modification sites resulted in different patterns of CE electropherograms for the tryptic digested mono-PEG-sCTs isomers, and the PEG modification sites were assigned accordingly. The PEG-modification sites were also confirmed directly by determining the molecular masses of the tryptic digested PEG-modified fragments of respective mono-PEG-sCT by the matrix-assisted laser desorption ionization time-of-flight (MALDI-TOF) mass spectrometry.
开发了一种毛细管电泳法(CE),用于测定单聚乙二醇修饰的鲑鱼降钙素(单聚乙二醇-sCTs)三种位置异构体的聚乙二醇修饰位点。聚乙二醇修饰位点对蛋白水解降解的抗性导致经胰蛋白酶消化的单聚乙二醇-sCTs异构体的CE电泳图谱呈现不同模式,并据此确定聚乙二醇修饰位点。通过基质辅助激光解吸电离飞行时间(MALDI-TOF)质谱法测定各单聚乙二醇-sCT经胰蛋白酶消化后的聚乙二醇修饰片段的分子量,也直接证实了聚乙二醇修饰位点。