Literature DB >> 28604816

Correction: Nitrosothiol-Trapping-Based Proteomic Analysis of S-Nitrosylation in Human Lung Carcinoma Cells.

Shani Ben-Lulu, Tamar Ziv, Pnina Weisman-Shomer, Moran Benhar.   

Abstract

[This corrects the article DOI: 10.1371/journal.pone.0169862.].

Entities:  

Year:  2017        PMID: 28604816      PMCID: PMC5467977          DOI: 10.1371/journal.pone.0179803

Source DB:  PubMed          Journal:  PLoS One        ISSN: 1932-6203            Impact factor:   3.240


The concentration unit for LPS is listed incorrectly in the third sentence under the subheading “Cell culture and treatment” in the Materials and Methods section. The correct sentence is: For this purpose, cells were serum starved for 24 h and then stimulated for 72 h with or without a cytokine mix that included lipopolysaccharide (LPS, 0.5 μg/ml), tumor necrosis factor (TNFα, 20 ng/ml), interferon-γ (IFN-γ, 10 ng/ml) and interleukin 1β (IL-1β, 10 ng/ml). The concentration unit for LPS in the caption for Fig 1C is also incorrect. Please see the corrected Fig 1 caption here.
Fig 1

SNO trapping-based analysis of S-Nitrosylation in A549 cells.

(A) Schematic of the proteomic approach. Digitonin cell lysates, obtained from A549 treated with NO donor or with cytokines are incubated with a thioredoxin (Trx) trap mutant, Trx(C35S). In the trap mutant the resolving cysteine is replaced by serine (-OH). The protein also contains a streptavidin binding peptide. Trx(C35S) forms mixed disulfide bonds with nitrosylated substrates and the resulting complexes are pulled-down using avidin agarose. Identification of nitrosylation sites is assisted by differential thiol labeling, involving the sequential application of N-ethylmaleimide (NEM) and iodoacetamide (IAM). Proteins captured in the Trx pull-down are analyzed by SDS-PAGE or liquid chromatography-tandem mass spectrometry (LC-MS/MS). (B) A549 cells were treated with or without 500 μM S-nitrosocysteine (CysNO) for 10 min and thereafter digitonin lysates were incubated with Trx(C35S). Proteins captured by Trx were released by DTT and then analyzed by SDS-PAGE. Gels were stained with Krypton fluorescent protein stain and visualized using the Odyssey infrared imaging system. (C) A549 cells were treated for 72 h with LPS (0.5 μg/ml) and a cytokine mixture that included TNFα (20 ng/ml), IFN-γ (10 ng/ml) and IL-1β (10 ng/ml). Trx-based trapping of nitrosylated proteins was performed as in B.

SNO trapping-based analysis of S-Nitrosylation in A549 cells.

(A) Schematic of the proteomic approach. Digitonin cell lysates, obtained from A549 treated with NO donor or with cytokines are incubated with a thioredoxin (Trx) trap mutant, Trx(C35S). In the trap mutant the resolving cysteine is replaced by serine (-OH). The protein also contains a streptavidin binding peptide. Trx(C35S) forms mixed disulfide bonds with nitrosylated substrates and the resulting complexes are pulled-down using avidin agarose. Identification of nitrosylation sites is assisted by differential thiol labeling, involving the sequential application of N-ethylmaleimide (NEM) and iodoacetamide (IAM). Proteins captured in the Trx pull-down are analyzed by SDS-PAGE or liquid chromatography-tandem mass spectrometry (LC-MS/MS). (B) A549 cells were treated with or without 500 μM S-nitrosocysteine (CysNO) for 10 min and thereafter digitonin lysates were incubated with Trx(C35S). Proteins captured by Trx were released by DTT and then analyzed by SDS-PAGE. Gels were stained with Krypton fluorescent protein stain and visualized using the Odyssey infrared imaging system. (C) A549 cells were treated for 72 h with LPS (0.5 μg/ml) and a cytokine mixture that included TNFα (20 ng/ml), IFN-γ (10 ng/ml) and IL-1β (10 ng/ml). Trx-based trapping of nitrosylated proteins was performed as in B.
  1 in total

1.  Nitrosothiol-Trapping-Based Proteomic Analysis of S-Nitrosylation in Human Lung Carcinoma Cells.

Authors:  Shani Ben-Lulu; Tamar Ziv; Pnina Weisman-Shomer; Moran Benhar
Journal:  PLoS One       Date:  2017-01-12       Impact factor: 3.240

  1 in total
  1 in total

1.  Stress-induced Changes in the S-palmitoylation and S-nitrosylation of Synaptic Proteins.

Authors:  Monika Zareba-Koziol; Anna Bartkowiak-Kaczmarek; Izabela Figiel; Adam Krzystyniak; Tomasz Wojtowicz; Monika Bijata; Jakub Wlodarczyk
Journal:  Mol Cell Proteomics       Date:  2019-07-16       Impact factor: 5.911

  1 in total

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