MassIVE MSV000082578

Partial Public

Metabolic niche adaptation of community- and hospital-associated methicillin-resistant Staphylococcus aureus

Description

Acquisition of mass spectrometry (MS) data was performed in the data-independent mode (DIA) mode by shotgun nano-liquid chromatography (LC)-MS/MS on a Q Exactive Plus (Thermo-Fisher Scientific, Waltham, MA, USA) connected to an Ultimate 3000 Nano LC as described before. Prior to the separation of samples by nano-HPLC, an iRT-spike-in-mix (Biognosys AG, Schlieren, Switzerland) was added to the samples. To construct strain-specific ion libraries, samples were measured in data-dependent mode (DDA) as described before. Sequence of the respective isolates was used to search for the database by MaxQuant. The Spectronaut Pulsar software package (v 11.0.15038.12.32941, Biognosys AG 2013) was used to analyse the samples in a strain-dependent manner. [dataset license: CC0 1.0 Universal (CC0 1.0)]

Keywords: Staphylococcus aureus, central carbon metabolism, adaptation, community-associated, hospital-associated, cytosolic protein, mass spectrometry.

Contact

Principal Investigators:
(in alphabetical order)
Uwe Voelker, Interfaculty Institute for Genetics and Functional Genomics, Department of Functional Genomics, Germany
Submitting User: solomonmekonnen
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Experimental Design
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Identification Results
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Quantification Results
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Originally identified proteins that were automatically remapped by MassIVE to proteins in the SwissProt human reference database.

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Distinct protein accessions are counted across all files submitted in the "Statistical Analysis of Quantified Analytes" category having a "Protein" column in this dataset.

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