Chan James Chun Yip, Zhou Lei, Chan Eric Chun Yong
Department of Pharmacy, National University of Singapore, Singapore.
Singapore Eye Research Institute, Singapore.
Curr Protoc Protein Sci. 2015 Nov 2;82:23.2.1-23.2.19. doi: 10.1002/0471140864.ps2302s82.
The isotope-coded affinity tag (ICAT) technique has been applied to measure pairwise changes in protein expression through differential stable isotopic labeling of proteins or peptides followed by identification and quantification using a mass spectrometer. Changes in protein expression are observed when the identical peptide from each of two biological conditions is identified and a difference is detected in the measurements comparing the peptide labeled with the heavy isotope to the one with a normal isotopic distribution. This approach allows the simultaneous comparison of the expression of many proteins between two different biological states (e.g., yeast grown on galactose versus glucose, or normal versus cancer cells). Due to the cysteine-specificity of the ICAT reagents, the ICAT technique has also been applied to perform relative quantitation of cysteine redox modifications such as oxidation and nitrosylation. This unit describes both protein quantitation and profiling of cysteine redox modifications using the ICAT technique.
同位素编码亲和标签(ICAT)技术已被应用于通过对蛋白质或肽进行差异稳定同位素标记,随后使用质谱仪进行鉴定和定量,来测量蛋白质表达的成对变化。当鉴定出两种生物学条件下各自相同的肽,并在比较重同位素标记的肽与具有正常同位素分布的肽的测量中检测到差异时,就会观察到蛋白质表达的变化。这种方法允许同时比较两种不同生物学状态(例如,在半乳糖与葡萄糖上生长的酵母,或正常细胞与癌细胞)之间许多蛋白质的表达。由于ICAT试剂对半胱氨酸具有特异性,ICAT技术也已被用于进行半胱氨酸氧化还原修饰(如氧化和亚硝基化)的相对定量。本单元描述了使用ICAT技术进行蛋白质定量和半胱氨酸氧化还原修饰分析的方法。