Proteomics

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Precision in Tear Fluid Biomarker Discovery: Quantitative Proteomic Profiling of Small-Volume, Individual Samples Using Capillary Tube Collection


ABSTRACT: Tear fluid, a complex biofluid that contains thousands of proteins and can be collected non-invasively, has emerged as a promising source of biomarkers for ocular and systemic health. Liquid chromatography-tandem mass spectrometry (LC-MS/MS) is currently the primary method for discovering novel biomarkers in tear fluid. However, the method of tear collection can sig-nificantly impact LC-MS/MS analysis outcomes. Tear fluid is commonly collected using either Schirmer strips or capillary tubes. While capillary tubes offer distinct advantages, such as reduced extracellular contamination and reflex tearing, most LC-MS/MS protocol development has focused on optimizing protocols for Schirmer strips. This study addresses this gap by evaluating digestion protocols for tear fluid collected with capillary tubes, focusing on biomarker discovery using small-volume samples. In this study, we evaluated multiple digestion protocols for the shotgun quantitative LC-MS/MS analysis of small-volume tear fluid samples collected using glass capillary tubes. Protocol optimization was performed using pooled samples and then compared with the analysis of individual samples. Using the optimized protocol, 0.5μL were processed using a timsTOF Pro 2 mass spectrometer (Bruker) coupled online with an Evosep One liquid chroma-tography system (Evosep), leading to the identification of an average of 368 ± 87 proteins in pooled samples and 502 ± 127 proteins in individual small-volume tear fluid samples. This protocol highlights the practicality of using glass capillary tubes for comprehensive LC-MS/MS-based tear proteomics analysis, paving the way for detailed proteomics characterization of individual tear fluid samples rather than pooled samples. By shifting from pooled to individual samples, this approach greatly accelerates tear biomarker discovery, advancing precision and personalized medicine.

INSTRUMENT(S): ultraflex, maXis, LTQ, LCQ Classic, Orbitrap Fusion, 6520A Quadrupole Time-of-Flight LC/MS, Orbitrap Fusion Lumos, Synapt MS, timsTOF Pro 2, 6410 Triple Quadrupole LC/MS, LTQ Orbitrap Elite, Q Exactive, LTQ Orbitrap, 6340 Ion Trap LC/MS, autoflex, LTQ Orbitrap Velos, 4800 Proteomics Analyzer, Q-Tof Ultima, LTQ FT, 6220 Time-of-Flight LC/MS, TripleTOF 5600, Q Exactive HF, MALDI Synapt MS, Q TRAP, QSTAR, 4700 Proteomics Analyzer

ORGANISM(S): Homo Sapiens (human)

TISSUE(S): Tear, Tear Secreting Cell

SUBMITTER: James Xiao  

LAB HEAD: Kunhong Xiao

PROVIDER: PXD060101 | Pride | 2025-05-07

REPOSITORIES: Pride

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Publications

Precision in Tear Fluid Biomarker Discovery: Quantitative Proteomic Profiling of Small-Volume, Individual Samples Using Capillary Tube Collection.

Frenia Kyla K   Fu Yunxiang Y   Beatty Maria A MA   Garwood Kathleen C KC   Kimmel Jeremy J   Raiji Veena V   Pan Dipanjan D   Bartlett David D   Labriola Leanne T LT   Xiao Kunhong K  

Biomedicines 20250206 2


<b>Background</b>: Tear fluid, rich in proteins, is a promising source of novel biomarkers for ocular and systemic health. Liquid chromatography-tandem mass spectrometry (LC-MS/MS) is the primary method for biomarker discovery. Still, factors such as limited sample volume, extracellular protein contamination, and reflex tearing can significantly impact results. Glass microcapillary tubes minimize these issues. Schirmer strips remain the most common collection method due to existing LC-MS/MS prot  ...[more]

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