Annovazzi Laura, Viglio Simona, Perani Eleonora, Luisetti Maurizio, Baraniuk James, Casado Begoña, Cetta Giuseppe, Iadarola Paolo
Dipartimento di Biochimica A Castellani, Università di Pavia, Italy.
Electrophoresis. 2004 Feb;25(4-5):683-91. doi: 10.1002/elps.200305607.
Among various biomarkers believed to behave as descriptors of the disease process in chronic obstructive pulmonary disease (COPD), urinary desmosines are commonly used for monitoring elastin degradation. Given the low concentrations of urinary desmosines, their quantitative determination in this biological matrix often requires preconcentration steps. To minimize both solute losses and effects of sample matrix, and to decrease data variability related to the above-mentioned manipulation processes, we have developed a capillary electrophoresis approach combined with laser-induced fluorescence (CE-LIF) detection system using urine samples not submitted to any pretreatment procedure other than filtering the sample. Urines were hydrolyzed, derivatized with fluorescein isothiocyanate (FITC) and endogenous desmosines were identified by addition of standard analytes and submitting to mass spectrometry (MS) analysis the material collected from micropreparative runs. The assay showed good linearity, reproducibility and precision, allowing to detect amounts of desmosines as low as 10(-8) M (equivalent to 0.1 fmol on column). We conclude that CE-LIF technique is a highly sensitive method for detecting urinary desmosines.
在被认为可作为慢性阻塞性肺疾病(COPD)疾病进程描述指标的各种生物标志物中,尿去甲基胶原吡啶交联常用于监测弹性蛋白降解。鉴于尿去甲基胶原吡啶交联的浓度较低,在这种生物基质中对其进行定量测定通常需要预浓缩步骤。为了使溶质损失和样品基质的影响最小化,并减少与上述操作过程相关的数据变异性,我们开发了一种毛细管电泳方法,结合激光诱导荧光(CE-LIF)检测系统,使用的尿样除过滤外未进行任何预处理。尿液经水解、用异硫氰酸荧光素(FITC)衍生化,通过添加标准分析物并对微量制备运行收集的材料进行质谱(MS)分析来鉴定内源性去甲基胶原吡啶交联。该测定法显示出良好的线性、重现性和精密度,能够检测低至10^(-8) M的去甲基胶原吡啶交联量(相当于柱上0.1 fmol)。我们得出结论,CE-LIF技术是检测尿去甲基胶原吡啶交联的一种高灵敏度方法。