Törnhage Carl-Johan, Peters Björn, Latosinska Agnieszka, Mina Ioanna K, Mokou Marika, Mischak Harald, Siwy Justyna
Region Västra Götaland, Skaraborg Hospital, Skövde, Sweden.
Institute of Clinical Science, Sahlgrenska Academy at University of Gothenburg, Gothenburg, Sweden.
Proteomics. 2025 Jul;25(13):e00231. doi: 10.1002/pmic.202400231. Epub 2025 May 27.
Proteins and peptides indicate physiological or pathological states and are investigated to identify markers to scrutinize health and disease surveillance. Saliva contains many proteins and peptides that could serve as biomarkers, offering a potential noninvasive approach for disease detection. To enable the assessment of the saliva proteome and peptidome as sources of biomarkers, protocols for sampling, sample preparation, and measurements have to be developed. We present the results of peptidome analysis from saliva samples collected at different time points before and after breakfast from 14 healthy adults (50% male, mean age 42.7 ± 10.3 years). While similar methods have been previously applied to urine, our aim was to adapt and demonstrate the effectiveness of these protocols for saliva. Specifically, we aimed to establish a salivary peptide dataspace, including peptide amino acid sequences, and to evaluate the impact of food intake and time of sampling. Capillary electrophoresis-mass spectrometry (CE-MS) and CE-MS/MS were used for peptidome analysis. Per sample, 3147 ± 559 peptides were detectable, without significant differences in the number of detected peptides between sample collection times. However, some peptides differed significantly in their abundance between samples collected before breakfast and 1, 2 and 4 h after breakfast. Samples collected after breakfast were more consistent in their peptide content. Sequencing identified 630 peptides, fragments of 82 proteins, with the majority derived from proline-rich proteins. The data indicate that saliva for peptidomics is best collected 1 to 4 h after breakfast.
蛋白质和肽可指示生理或病理状态,人们对其进行研究以识别用于仔细审查健康和疾病监测的标志物。唾液含有许多可作为生物标志物的蛋白质和肽,为疾病检测提供了一种潜在的非侵入性方法。为了能够将唾液蛋白质组和肽组评估为生物标志物的来源,必须制定采样、样品制备和测量的方案。我们展示了对14名健康成年人(50%为男性,平均年龄42.7±10.3岁)在早餐前后不同时间点采集的唾液样本进行肽组分析的结果。虽然之前已将类似方法应用于尿液,但我们的目的是调整并证明这些方案对唾液的有效性。具体而言,我们旨在建立一个唾液肽数据空间,包括肽氨基酸序列,并评估食物摄入和采样时间的影响。毛细管电泳-质谱(CE-MS)和CE-MS/MS用于肽组分析。每个样本可检测到3147±559个肽,样本采集时间之间检测到的肽数量没有显著差异。然而,一些肽在早餐前采集的样本与早餐后1、2和4小时采集的样本之间丰度存在显著差异。早餐后采集的样本肽含量更一致。测序鉴定出630个肽,为82种蛋白质的片段,其中大多数来自富含脯氨酸的蛋白质。数据表明,用于肽组学研究的唾液最好在早餐后1至4小时采集。