Lanz Christian, Kuhn Martina, Bortolotti Federica, Tagliaro Franco, Thormann Wolfgang
University of Bern, Department of Clinical Pharmacology, Murtenstrasse 35, CH-3010 Bern, Switzerland.
J Chromatogr A. 2002 Dec 6;979(1-2):43-57. doi: 10.1016/s0021-9673(02)01244-x.
Serum transferrin (Tf) comprises several isoforms with up to two complex oligosaccharide chains containing zero to eight sialic acid residues and neutral sugars. The major glycoform, known as tetrasialo-Tf, contains four sialic acid residues and accounts for about 80% of whole Tf in human serum. Carbohydrate-deficient transferrin (CDT) encompasses isoforms that are deficient in carbohydrate chains and consequently in sialic acid residues (including asialo-, monosialo- and disialo-Tf) and is a well known marker for chronic alcohol abuse. Recently capillary zone electrophoresis (CZE) has been reported as a tool extremely effective for the simultaneous, individual, quantitative determination of CDT isoforms. Three CZE methods that feature different dynamic capillary coatings were evaluated and optimized for CDT determination in human serum of alcohol abusers and control subjects. CZE separation was performed in alkaline borate buffers after serum sample saturation with iron, electropherograms were detected at 200 nm, data were evaluated as % area of disialo-Tf in relation to tetrasialo-Tf and peak identification was accomplished via relative migration times to tetrasialo-Tf, immunosubtraction and enzymatic sequential cleavage of sialic acid residues. Dynamic capillary coatings with diaminobutane, spermine and a double coating produced by commercially available proprietary agents were investigated and found to be suitable for determination of CDT in human serum. For all three approaches, best results were obtained in 50 microm I.D. fused-silica capillaries of 50 cm effective length and a capillary cartridge temperature of 20-25 degrees C. Using 3 mM 1,4-diaminobutane or 0.02 mM spermine in a borate-based running buffer of pH 8.3 provided data of remarkable similarity with resolution of di-, tri-, tetra- and pentasialo-Tf within 15-18 min. With the double coating, asialo-Tf and Tf isoforms with two to six sialic acid residues were baseline separated. Compared to the two amine-based procedures, the run times were found to be somewhat shorter, the detector signals higher, the applied power level significantly lower and the reproducibility better.
血清转铁蛋白(Tf)由几种同工型组成,带有多达两条复杂的寡糖链,这些寡糖链含有零至八个唾液酸残基和中性糖。主要的糖型,即四唾液酸转铁蛋白,含有四个唾液酸残基,约占人血清中总Tf的80%。碳水化合物缺乏转铁蛋白(CDT)包括碳水化合物链缺乏因而唾液酸残基缺乏的同工型(包括无唾液酸、单唾液酸和双唾液酸转铁蛋白),是慢性酒精滥用的一个众所周知的标志物。最近,毛细管区带电泳(CZE)已被报道为一种极其有效的工具,可同时、单独、定量测定CDT同工型。评估并优化了三种具有不同动态毛细管涂层的CZE方法,用于测定酗酒者和对照受试者人血清中的CDT。血清样品用铁饱和后,在碱性硼酸盐缓冲液中进行CZE分离,在200nm处检测电泳图,数据以双唾液酸转铁蛋白相对于四唾液酸转铁蛋白的面积百分比进行评估,通过相对于四唾液酸转铁蛋白的相对迁移时间、免疫扣除和唾液酸残基的酶促顺序裂解来完成峰识别。研究了用丁二胺、精胺以及市售专有试剂产生的双重涂层的动态毛细管涂层,发现它们适用于测定人血清中的CDT。对于所有三种方法,在内径50μm、有效长度50cm且毛细管柱温度为20 - 25℃的熔融石英毛细管中可获得最佳结果。在pH 8.3的硼酸盐运行缓冲液中使用3mM 1,4 - 丁二胺或0.02mM精胺,可在15 - 18分钟内实现二、三、四和五唾液酸转铁蛋白的分离,得到的数据具有显著相似性。使用双重涂层时,无唾液酸转铁蛋白和带有两至六个唾液酸残基的转铁蛋白同工型实现了基线分离。与两种基于胺的方法相比,发现运行时间稍短,检测信号更高,施加的功率水平显著更低且重现性更好。