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基于磁珠的唾液肽组分析在正畸治疗期间的应用。

Magnetic bead-based salivary peptidome profiling analysis during orthodontic treatment durations.

机构信息

Department of Orthodontics, School of Stomatology, Peking University, Beijing 100081, PR China.

出版信息

Biochem Biophys Res Commun. 2012 May 18;421(4):844-9. doi: 10.1016/j.bbrc.2012.04.100. Epub 2012 Apr 25.

Abstract

Orthodontic treatment induces various biological responses, including tooth movement and remodeling of alveolar bone. Although some studies have investigated the contribution of orthodontic procedures to changes in saliva conditions, little is known about the effects of different treatment durations on the saliva proteome. To identify the discriminating protein profiles in unstimulated whole saliva of orthodontic patients with different treatment durations, we used matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS) combined with magnetic bead, and peptide mass fingerprints were created by scanning MS signals. Saliva samples from 40 patients (10 in each of four groups: the group without an appliance and groups under treatment for 2, 7, and 12 months) were analyzed. The results showed eight mass peaks with significant differences. Furthermore, mass peak intensities at proteins 1817.7, 2010.7, 2744 and 2710.2 Da represented a steady time-dependent increasing trend, whereas protein 4134 Da exhibited a decreasing tendency. Differential expression of the peptidome profile also occurred in the multiple comparisons, and we established a fitting model. Thus, the potential discriminating biomarkers investigated in this study reflected the complicated changes in periodontal tissues during orthodontic treatment and indicated dynamic interactions between orthodontic treatment and the saliva proteome. The results provide novel insights into alterations in salivary proteins due to different orthodontic treatment durations and may lead to the development of a therapeutic monitoring strategy for orthodontics.

摘要

正畸治疗会引起各种生物学反应,包括牙齿移动和牙槽骨改建。尽管一些研究已经调查了正畸过程对唾液条件变化的贡献,但对于不同治疗时间对唾液蛋白质组的影响知之甚少。为了鉴定不同治疗时间的正畸患者未刺激全唾液中的区分蛋白图谱,我们使用基质辅助激光解吸/电离飞行时间质谱(MALDI-TOF MS)结合磁珠,通过扫描 MS 信号创建肽质量指纹图谱。分析了 40 名患者(每组 10 名,无矫治器组和治疗 2、7 和 12 个月组)的唾液样本。结果显示有 8 个质量峰有显著差异。此外,蛋白 1817.7、2010.7、2744 和 2710.2 Da 的质量峰强度呈现出稳定的时间依赖性增加趋势,而蛋白 4134 Da 则表现出下降趋势。在多次比较中,肽组图谱的差异表达也发生了变化,我们建立了一个拟合模型。因此,本研究中研究的潜在区分生物标志物反映了正畸治疗期间牙周组织的复杂变化,并表明了正畸治疗与唾液蛋白质组之间的动态相互作用。这些结果为不同正畸治疗时间导致的唾液蛋白变化提供了新的见解,并可能为正畸治疗的治疗监测策略的发展提供依据。

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