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SWATH Based Quantitative Proteomics Reveals Significant Lipid Metabolism in Early Myopic Guinea Pig Retina. | LitMetric

AI Article Synopsis

  • - The study critiques previous research on myopia that used only one candidate and less advanced proteomics techniques, leading to incomplete understanding of molecular changes in the retina during myopia development.
  • - Researchers conducted a high-resolution proteomic analysis on guinea pigs after inducing myopia, identifying over 3,200 proteins and finding significant changes in 37 up-regulated and 21 down-regulated proteins.
  • - The top function linked to these changes was "lipid metabolism," and two proteins in this pathway were validated using a novel assay, advancing our knowledge of the molecular events related to early myopia.

Article Abstract

Most of the previous myopic animal studies employed a single-candidate approach and lower resolution proteomics approaches that were difficult to detect minor changes, and generated limited systems-wide biological information. Hence, a complete picture of molecular events in the retina involving myopic development is lacking. Here, to investigate comprehensive retinal protein alternations and underlying molecular events in the early myopic stage, we performed a data-independent Sequential Window Acquisition of all Theoretical Mass Spectra (SWATH) based proteomic analysis coupled with different bioinformatics tools in pigmented guinea pigs after 4-day lens-induced myopia (LIM). Myopic eyes compared to untreated contralateral control eyes caused significant changes in refractive error and choroid thickness ( < 0.05, = 5). Relative elongation of axial length and the vitreous chamber depth were also observed. Using pooled samples from all individuals ( = 10) to build a species-specific retinal ion library for SWATH analysis, 3202 non-redundant proteins (with 24,616 peptides) were identified at 1% global FDR. For quantitative analysis, the 10 individual retinal samples (5 pairs) were analyzed using a high resolution Triple-TOF 6600 mass spectrometry (MS) with technical replicates. In total, 37 up-regulated and 21 down-regulated proteins were found significantly changed after LIM treatment (log2 ratio (T/C) > 0.26 or < -0.26; ≤ 0.05). Data are accepted via ProteomeXchange with identifier PXD025003. Through Ingenuity Pathways Analysis (IPA), "lipid metabolism" was found as the top function associated with the differentially expressed proteins. Based on the protein abundance and peptide sequences, expression patterns of two regulated proteins ( and ) identified in this pathway were further successfully validated with high confidence ( < 0.05) using a novel Multiple Reaction Monitoring (MRM) assay on a QTRAP 6500+ MS. In summary, through an integrated discovery and targeted proteomic approach, this study serves as the first report to detect and confirm novel retinal protein changes and significant biological functions in the early LIM mammalian guinea pigs. The study provides new workflow and insights for further research to myopia control.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8124159PMC
http://dx.doi.org/10.3390/ijms22094721DOI Listing

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