Department of Applied Chemistry, National Chi Nan University, Puli, Nantou 545, Taiwan.
Analyst. 2011 May 7;136(9):1922-7. doi: 10.1039/c0an01046d. Epub 2011 Mar 14.
Simultaneous detection of multiply and singly phosphorylated peptides using matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS) is challenging because of suppression effects during ionization. In oder to overcome this problem, this study presents a new approach to improve the detection of phosphopeptides by stepwise enrichment using polyarginine-coated (PA-coated) and titanium dioxide-coated (TiO(2)-coated) nanodiamonds for fractionation of multiply and singly phosphorylated peptides prior to on-probe MALDI MS analysis. The feasibility of this approach was demonstrated using synthetic peptides containing different numbers of phosphate groups, tryptic digests of α-casein, β-casein, and complex protein mixtures. The high specificity of the approach is shown in its effective enrichment and fractionation of phosphopeptides from the digest of β-casein and bovine serum albumin at a molar ratio as low as 1 : 1000, which out-performs the commercial Fe(3+)-IMAC and TiO(2) isolation kits. It offers a simple and effective alternative for the fractionation and identification of multiply and singly phosphorylated peptides by MALDI MS and allows for deduction of more information from limited starting materials.
使用基质辅助激光解吸/电离飞行时间质谱(MALDI-TOF MS)同时检测多磷酸化肽和单磷酸化肽具有挑战性,因为在电离过程中存在抑制效应。为了克服这个问题,本研究提出了一种新的方法,通过分步富集来改善磷酸肽的检测,使用多聚精氨酸涂层(PA 涂层)和二氧化钛涂层(TiO 2 涂层)纳米金刚石对多磷酸化肽和单磷酸化肽进行分级,然后进行探针 MALDI MS 分析。使用含有不同数量磷酸基团的合成肽、α-酪蛋白、β-酪蛋白和复杂蛋白质混合物的胰蛋白酶消化物来证明这种方法的可行性。该方法的高特异性表现在其能够有效富集和分级β-酪蛋白和牛血清白蛋白消化物中的磷酸肽,即使在摩尔比低至 1:1000 的情况下,其性能优于商业的 Fe 3+ -IMAC 和 TiO 2 分离试剂盒。它为 MALDI MS 对多磷酸化肽和单磷酸化肽的分级和鉴定提供了一种简单有效的替代方法,并允许从有限的起始材料中推断出更多的信息。