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使用磷酸化括号进行精确的磷酸化位点定位。

Accurate phosphorylation site localization using phospho-brackets.

机构信息

School of Chemical Science & Engineering, Tongji University, Shanghai 200092, China; Shanghai Key Laboratory of Chemical Assessment and Sustainability, Tongji University, Shanghai 200092, China.

School of Chemical Science & Engineering, Tongji University, Shanghai 200092, China; Shanghai Key Laboratory of Chemical Assessment and Sustainability, Tongji University, Shanghai 200092, China.

出版信息

Anal Chim Acta. 2017 Dec 15;996:38-47. doi: 10.1016/j.aca.2017.09.043. Epub 2017 Oct 17.

Abstract

Phosphorylation is one of the most important and widely studied protein post-translational modifications. Tandem mass spectrometry using higher-energy collisional dissociation has evolved into a state-of-the-art analytical platform for both phosphorylation identification and site localization. Tens of thousands of phosphopeptides can now be routinely identified from a single shotgun proteomics study; site localization, however, is much more complicated and many challenges still exist. Here, we report our development of P-bracket using direct experimental evidence of phospho-containing site-determining product ions for accurate site localization without the need for additional FLR control. A P-bracket is defined as a complementary product ion pair that forms a bracket to confine a phosphorylation event to a unique site. P-bracket has been successfully benchmarked with a set of six synthetic phosphopeptides with a single phosphorylation event, a set of 96 synthetic peptides and phosphopeptide reference libraries, and two HeLa phosphopeptide LC-MS/MS (HCD) datasets; Accurate phosphosite localization by P-bracket will greatly enhance identification confidence of phosphopeptides and contribute to structural and functional studies of phosphoproteins.

摘要

磷酸化是最重要和研究最广泛的蛋白质翻译后修饰之一。使用更高能量碰撞解离的串联质谱已发展成为鉴定磷酸化和定位位点的最先进的分析平台。现在,从单个鸟枪法蛋白质组学研究中可以常规鉴定数万种磷酸肽;然而,位点定位要复杂得多,仍然存在许多挑战。在这里,我们报告了我们使用含有磷酸化的位点确定产物离子的直接实验证据来开发 P 支架,以实现准确的位点定位,而无需额外的 FLR 控制。P 支架被定义为形成支架的互补产物离子对,将磷酸化事件限制在唯一的位点上。P 支架已经成功地与一组具有单个磷酸化事件的六种合成磷酸肽、一组 96 种合成肽和磷酸肽参考文库以及两个 HeLa 磷酸肽 LC-MS/MS (HCD) 数据集进行了基准测试;P 支架的准确磷酸化位点定位将大大提高磷酸肽的鉴定置信度,并有助于磷酸化蛋白的结构和功能研究。

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