Greer Tyler, Li Lingjun
Department of Chemistry, University of Wisconsin-Madison, Madison, WI, 53706, USA.
School of Pharmacy, University of Wisconsin-Madison, 777 Highland Avenue, Madison, WI, 53705-2222, USA.
Methods Mol Biol. 2016;1410:195-206. doi: 10.1007/978-1-4939-3524-6_11.
Quantitative proteomics studies require an absolute quantification step to accurately measure changes in protein concentration. Absolute quantification using liquid chromatography-mass spectrometry (LC-MS) traditionally combines triple quadrupole instrumentation with stable isotope-labeled standards to measure protein concentrations via their enzymatically produced peptides. Chemical modification of peptides using labels like mass differential tags for relative and absolute quantification (mTRAQ) provides another route to determine protein quantities. This chapter describes a cost-effective and high-throughput chemical labeling method that utilizes five amine-reactive, isotopic N,N-dimethyl leucine (iDiLeu) reagents. These tags enable generation of four-point calibration curves in one LC-MS run to determine protein concentrations from labeled peptides. In particular, we provide a detailed workflow for protein quantification using the iDiLeu reagent that includes important considerations like labeling conditions and isotopic interference correction.
定量蛋白质组学研究需要一个绝对定量步骤来准确测量蛋白质浓度的变化。传统上,使用液相色谱 - 质谱联用(LC-MS)进行绝对定量是将三重四极杆仪器与稳定同位素标记的标准品相结合,通过酶促产生的肽段来测量蛋白质浓度。使用如用于相对和绝对定量的质量差异标签(mTRAQ)等标签对肽段进行化学修饰,为确定蛋白质数量提供了另一种途径。本章介绍了一种经济高效且高通量的化学标记方法,该方法利用了五种胺反应性、同位素N,N - 二甲基亮氨酸(iDiLeu)试剂。这些标签能够在一次LC-MS运行中生成四点校准曲线,以便从标记的肽段中确定蛋白质浓度。特别是,我们提供了使用iDiLeu试剂进行蛋白质定量的详细工作流程,其中包括标记条件和同位素干扰校正等重要注意事项。