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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

Cytokines in the grass, a lesson learnt: Measuring cytokines in plasma using multiple reaction monitoring mass spectrometry

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Author(s):
Mendoza-Porras, Omar [1] ; Pires, Pedro R. L. [1, 2] ; Goswami, Hareshwar [1] ; Meirelles, Flavio V. [2] ; Colgrave, Michelle L. [1] ; Wijffels, Gene [1]
Total Authors: 6
Affiliation:
[1] CSIRO Agr & Food, 306 Carmody Rd, St Lucia, Qld 4067 - Australia
[2] Univ Sao Paulo, Ave Duque de Caxais Morte 225, Sao Paulo - Brazil
Total Affiliations: 2
Document type: Journal article
Source: RAPID COMMUNICATIONS IN MASS SPECTROMETRY; v. 34, n. 9 MAY 15 2020.
Web of Science Citations: 0
Abstract

Rationale Cytokines are cell regulatory molecules of high importance as indicators for homeostasis and pathology in many species. The current method to measure cytokines in body fluids is reagent dependent, requiring highly specific paired antibodies. Methods A liquid chromatography/multiple reaction monitoring mass spectrometry (LC/MRM-MS)-based approach was developed to simultaneously establish the limits of detection (LODs) and quantification (LOQs) for recombinant cytokines IL-1 beta, IL-6, IFN gamma and TNF alpha as pure standards and in bovine sera. All experimental LC/MRM-MS data are available at CSIRO Data Access Portal repository under identifier . Results The present method enabled LODs and LOQs as low as 1.05 and 1.12 fmol/mu L in the experiment comprised of pure standards. Comparable results were obtained in the experiment where digested cytokines were mixed with pre-digested sera proteins. The intrinsic matrix effects were evident when intact cytokines were co-digested within undiluted and undigested sera decreasing the ability to detect and quantify cytokines by 10,000-fold compared with pure standards and pre-digested sera. Conclusions The developed LC/MRM-MS method provided insights into the difficulties in detecting the target peptides when embedded in complex matrices. Nonetheless, the method may potentially be readily applied in biomarker-focused research interrogating fluids of lesser complexity such as synovial fluid, cerebrospinal fluid and tissue culture media. (AU)

FAPESP's process: 14/05405-1 - Development and validation of Multiplexed bovine plasma cytokine measurement using multiple reaction monitoring (MRM) mass spectrometry
Grantee:Pedro Ratto Lisboa Pires
Support Opportunities: Scholarships abroad - Research Internship - Doctorate