首页> 美国卫生研究院文献>Molecular Cellular Proteomics : MCP >Targeted Proteomics Guided by Label-free Quantitative Proteome Analysis in Saliva Reveal Transition Signatures from Health to Periodontal Disease
【2h】

Targeted Proteomics Guided by Label-free Quantitative Proteome Analysis in Saliva Reveal Transition Signatures from Health to Periodontal Disease

机译:唾液中无标签定量蛋白质组分析指导的靶向蛋白质组学揭示了从健康到牙周疾病的转变特征

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Periodontal diseases are among the most prevalent worldwide, but largely silent, chronic diseases. They affect the tooth-supporting tissues with multiple ramifications on life quality. Their early diagnosis is still challenging, due to lack of appropriate molecular diagnostic methods. Saliva offers a non-invasively collectable reservoir of clinically relevant biomarkers, which, if utilized efficiently, could facilitate early diagnosis and monitoring of ongoing disease. Despite several novel protein markers being recently enlisted by discovery proteomics, their routine diagnostic application is hampered by the lack of validation platforms that allow for rapid, accurate and simultaneous quantification of multiple proteins in large cohorts. Here we carried out a pipeline of two proteomic platforms; firstly, we applied open ended label-free quantitative (LFQ) proteomics for discovery in saliva (n = 67, including individuals with health, gingivitis, and periodontitis), followed by selected-reaction monitoring (SRM)-targeted proteomics for validation in an independent cohort (n = 82). The LFQ platform led to the discovery of 119 proteins with at least 2-fold significant difference between health and disease. The 65 proteins chosen for the subsequent SRM platform included 50 functionally related proteins derived from the significantly enriched processes of the LFQ data, 11 from literature-mining, and four house-keeping ones. Among those, 60 were reproducibly quantifiable proteins (92% success rate), represented by a total of 143 peptides. Machine-learning modeling led to a narrowed-down panel of five proteins of high predictive value for periodontal diseases with maximum area under the receiver operating curve >0.97 (higher in disease: Matrix metalloproteinase-9, Ras-related protein-1, Actin-related protein 2/3 complex subunit 5; lower in disease: Clusterin, Deleted in Malignant Brain Tumors 1). This panel enriches the pool of credible clinical biomarker candidates for diagnostic assay development. Yet, the quantum leap brought into the field of periodontal diagnostics by this study is the application of the biomarker discovery-through-verification pipeline, which can be used for validation in further cohorts.
机译:牙周疾病是世界上最流行的疾病,但大部分是无声的慢性疾病。它们会影响生活质量,对牙齿支撑组织产生多种影响。由于缺乏适当的分子诊断方法,它们的早期诊断仍然具有挑战性。唾液提供了无创收集的临床相关生物标记物,如果有效利用,将有助于早期诊断和监测正在进行的疾病。尽管发现蛋白质组学最近招募了几种新颖的蛋白质标记,但由于缺乏可对大型人群中多种蛋白质进行快速,准确和同时定量的验证平台,它们的常规诊断应用受到了阻碍。在这里,我们进行了两个蛋白质组学平台的开发;首先,我们应用开放式无标签定量蛋白质组学(LFQ)在唾液中发现(n = 67,包括有健康,牙龈炎和牙周炎的个体),然后选择针对选择性反应监测(SRM)的蛋白质组学进行验证。独立队列(n = 82)。 LFQ平台导致发现119种蛋白质,其健康与疾病之间的差异至少有2倍。为随后的SRM平台选择的65种蛋白质包括50种功能相关的蛋白质,这些蛋白质来自LFQ数据的显着丰富过程,11种来自文献挖掘和4种内部管理。在这些蛋白中,有60种是可重复定量的蛋白(成功率92%),总共143个肽。机器学习模型缩小了对牙周疾病具有高预测价值的五种蛋白质的范围,在接收器工作曲线下的最大面积> 0.97(疾病较高:基质金属蛋白酶9,Ras相关蛋白1,肌动蛋白-相关蛋白2/3复合亚基5;疾病较低:Clusterin,在恶性脑肿瘤中缺失1)。该小组丰富了用于诊断测定开发的可靠临床生物标志物候选物库。然而,这项研究带入了牙周诊断领域的巨大飞跃是生物标志物通过验证发现管道的应用,该管道可用于进一步的队列验证。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号