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两步一步式的免洗、免分离粒子上的离子化/富集:多功能 TiO2 纳米粒子作为脱盐、加速和亲和探针,用于微波辅助酶解 ESI-MS 和 MALDI-MS 中的磷酸化蛋白:与微尺度 TiO2 的比较。

Two-step on-particle ionization/enrichment via a washing- and separation-free approach: multifunctional TiO2 nanoparticles as desalting, accelerating, and affinity probes for microwave-assisted tryptic digestion of phosphoproteins in ESI-MS and MALDI-MS: comparison with microscale TiO2.

机构信息

Department of Chemistry, National Sun Yat-Sen University, 70, Lien-Hai Road, Kaohsiung 80424, Taiwan.

出版信息

Anal Bioanal Chem. 2010 Apr;396(8):2909-19. doi: 10.1007/s00216-010-3573-3. Epub 2010 Mar 16.

Abstract

We introduce a simplified sample preparation method using bare TiO(2) nanoparticles (NPs) to serve as multifunctional nanoprobes (desalting, accelerating, and affinity probes) for effective enrichment of phosphopeptides from microwave-assisted tryptic digestion of phosphoproteins (alpha-casein, beta-casein and milk) in Electrospray Ionization Mass Spectrometry (ESI-MS) and Matrix Assisted Laser Desorption Ionization Mass Spectrometry (MALDI-MS). The results demonstrate that TiO(2) NPs can effectively enrich and accelerate the digestion reactions of phosphoproteins in aqueous solutions and also from complex real samples. After the microwave experiments, we directly injected the resulting solutions into the ESI-MS and MALDI-MS systems for analysis, and excellent sensitivity was achieved without the need for any washing procedure or separation process. The reasons are attributed to the high binding affinity and selectivity of TiO(2) NPs toward phosphopeptides. Thus, phosphopeptides can be adsorbed onto the TiO(2) NP surface. The digested or partially digested phosphoproteins can be concentrated onto the TiO(2) NP surface. This results in the effective or complete digestion of phosphoproteins in a short period of time (45 s). In addition, high sensitivity and sequence coverage of phosphopeptide can be obtained using TiO(2) NPs as microwave absorbers and affinity probes in MALDI-MS and ESI-MS. This is due to the photocatalytic nature of the TiO(2) NPs because the absorption of microwave radiation that can accelerate the activation of trypsin for efficient digestion of phosphoproteins and enhances the ionization of phosphopeptides. The lowest concentrations detected for ESI-MS and MALDI-MS were 0.1 microM and 10 fmol, respectively, for alpha-casein. Comparing the two-step approach of TiO(2) NPs with microscale TiO(2) particles, the microscale TiO(2) particles shows no effect on the microwave-assisted tryptic digestion of phosphoproteins. The current approach offers multiple advantages, such as great simplicity, high sensitivity and selectivity, straightforward and separation/washing-free technique for phosphopeptide enrichment analysis.

摘要

我们介绍了一种简化的样品制备方法,使用裸露的 TiO(2) 纳米粒子 (NPs) 作为多功能纳米探针(脱盐、加速和亲和探针),用于从微波辅助的磷酸化蛋白(α-酪蛋白、β-酪蛋白和牛奶)的胰蛋白酶消化中有效富集电喷雾电离质谱 (ESI-MS) 和基质辅助激光解吸电离质谱 (MALDI-MS) 中的磷酸肽。结果表明,TiO(2) NPs 可以有效地富集和加速水溶液中和复杂实际样品中磷酸化蛋白的消化反应。微波实验后,我们直接将所得溶液注入 ESI-MS 和 MALDI-MS 系统进行分析,无需任何洗涤或分离过程即可获得出色的灵敏度。原因归因于 TiO(2) NPs 对磷酸肽的高结合亲和力和选择性。因此,磷酸肽可以吸附在 TiO(2) NP 表面上。已消化或部分消化的磷酸化蛋白可以浓缩到 TiO(2) NP 表面上。这导致磷酸化蛋白在短时间内(45 秒)有效或完全消化。此外,TiO(2) NPs 作为微波吸收剂和亲和探针在 MALDI-MS 和 ESI-MS 中可以获得高灵敏度和磷酸肽的序列覆盖率。这是由于 TiO(2) NPs 的光催化性质,因为吸收微波辐射可以加速胰蛋白酶的活化,从而有效消化磷酸化蛋白,并增强磷酸肽的电离。对于 ESI-MS 和 MALDI-MS,检测到的最低浓度分别为 0.1 microM 和 10 fmol,用于 α-酪蛋白。与 TiO(2) NPs 的两步法相比,微尺度 TiO(2) 颗粒对微波辅助的磷酸化蛋白的胰蛋白酶消化没有影响。当前方法具有许多优点,例如简单、高灵敏度和选择性、直接且无需分离/洗涤的磷酸肽富集分析技术。

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