10 research outputs found

    Novel Small Molecule Matrix Screening for Simultaneous MALDI Mass Spectrometry Imaging of Multiple Lipids and Phytohormones

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    Most of the traditional matrices cannot simultaneously image multiple lipids and phytohormones, so screening and discovery of novel matrices stand as essential approaches for broadening the application scope of matrix-assisted laser desorption/ionization mass spectrometry imaging (MALDI-MSI). In this work, 12 organic small molecule compounds were comprehensively screened and investigated as potential MALDI matrices for simultaneous imaging analysis of various lipids and phytohormones. In the positive ionization mode, p-nitroaniline, m-nitroaniline, and 2-aminoterephthalic acid displayed good performance for the highly sensitive detection of lysophosphatidylcholines (LPCs), phosphatidylcholines (PCs), and triacylglycerols (TGs). Furthermore, p-nitroaniline possessed excellent characteristics of strong ultraviolet absorption and homogeneous cocrystallization, making it a desirable matrix for MALDI-MSI analysis of eight plant hormones. Compared with conventional matrices (2,5-dihydroxybenzoic acid (DHB), α-cyano-4-hydroxycinnamic acid (CHCA), and 9-aminoacridine (9-AA), the use of p-nitroaniline resulted in higher ionization efficiency, superior sensitivity, and clearer imaging images in dual polarity mode. Our research offers valuable guidance and new ideas for future endeavors in matrix screening

    Tracking Spatial Distribution Alterations of Multiple Endogenous Molecules during Lentil Germination by MALDI Mass Spectrometry Imaging

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    Exploring the spatial distribution alterations of metabolites during lentil germination is essential to reveal the nutritional value, physiological function, and metabolic pathway in lentils. Hence, an effective matrix-assisted laser desorption/ionization mass spectrometry imaging (MALDI-MSI) method was established for the first time to visualize the spatial localization changes of 53 metabolites in lentils during germination for 12–72 h. The results of MALDI-MSI analysis showed that phosphatidylinositols, phosphatidylethanolamines, phosphatidylglycerols, and phosphatidic acids were mainly located in the cotyledons of lentils throughout the germination process, while triacylglycerols, phosphatidylcholines, diacylglycerols, amino acids, choline, and spermine spread throughout the lentil tissue at the initial stage of germination and gradually presented obvious distribution characteristics in the radicle with increasing germination time. Heat map analysis was used to visualize the correlations between lipid content changes and germination time, which supported the use of germinated lentils as nutraceutical or functional food

    miR-132/182 regulating BDNF expression.

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    <p>(<b>A, B</b>) Detection of BDNF by western blotting. SH-SY5Y cells were treated with miR-182 or miR-132, the results showed that BDNF expression in the miR-182- or miR-132-treated cultures was much lower than that of negative control miRNA cultures. *<i>P</i><0.05, miR-182- or miR-132-treated cultures <i>vs.</i> control cultures. Relative values for BDNF <i>vs</i>. Actin are indicated in <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0063648#pone-0063648-g002" target="_blank">Fig.2B</a>.</p

    Relationship between levels of serum BDNF and its related miRNAs.

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    <p>(<b>A</b>) A significant negative correlation (Spearman <i>r<sub>s</sub></i> = −0.307, <i>P = </i>0.006) between the serum BDNF and miR-132 levels in depressed patients (n = 40) and controls (n = 40). (<b>B</b>) No significant correlation (Spearman <i>r<sub>s</sub></i> = 0.098, <i>P = </i>0.385) was found between the serum BDNF and miR-182 levels in depressed patients (n = 40) and controls (n = 40).</p

    BDNF serum levels and its related miRNAs.

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    <p>(<b>A</b>) BDNF concentrations in patients and controls. The serum levels of BDNF in the patients with depression (n = 40; 20.05±5.98 ng/ml) were significantly decreased compared with those of the healthy controls (n = 40; 25.22±5.17 ng/ml). (<b>B</b>) The targeting site on BDNF-mRNA-3′UTR by miR-182, which was aligned with the mRNA-3′UTR of human <i>bdnf</i> gene with the nucleotide position. Vertical lines indicate identity.</p
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