Heat inactivation

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PE-NMe (44:4) (1)
PE-NMe(42:4) (1)
Phosphatidylinositol (P-36:5) (1)
Ganglioside GM3 (36:2) (1)
Phosphatidic acid (P-36:3) (1)
Cardiolipin 78:13(2-) (1)
Cardiolipin 78:11(2-) (1)
CL(79:2) (1)
Phosphatidylethanolamine 40:3 zwitterion (1)
Phosphatidylethanolamine 36:5 zwitterion (1)
Phosphatidylethanolamine 32:1 zwitterion (1)
Phosphatidylethanolamine 42:2 (1)
PE-NMe(36:4) (1)
Phosphatidylglycerol 32:1(1-) (1)
CL(73:0) (1)
Phosphatidylserine 40:1(1-) (1)
Cardiolipin 78:14(2-) (1)
Phosphatidylinositol 42:6(1-) (1)
PG(O-34:0) (1)
Phosphatidylethanolamine 42:3 zwitterion (1)
Cardiolipin 76:10(2-) (1)
Phosphatidylethanolamine 38:2 zwitterion (1)
PE(39:0) (1)
PE-NMe(42:1) (1)
CL(74:0) (1)
Cardiolipin 72:8(2-) (1)
Phosphatidylethanolamine O-36:1 zwitterion (1)
Phosphatidylethanolamine 38:4 (1)
CL(78:0) (1)
Phosphatidylethanolamine P-36:5 (1)

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4x(2)H labeled dimethylated L-lysine (1)
N6-dimethyl-L-lysine (1)

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Lab affiliation

University of Vienna, Faculty of Chemistry, Department of Analytical Chemistry (3)
CEA-Marcoule, ProGénoMIX platform, DRF-Li2D, 30207 Bagnols-sur-Cèze, France (2)
Department of Chemistry and Bioscience Aalborg University Denmark (2)
Institute of Biochemistry II, Goethe University, Medical School, Frankfurt, Germany (2)
Proteomics Lab, 304, BSBE Department, Indian Institute Technology Bombay, Powai, Mumbai, India-400076 (2)
University of Louisville, Department of Chemistry, Louisville, KY 40208, USA (2)
1Department of Biochemistry and Microbiology, Ghent University, Ghent, Belgium (1)
Bavarian Center for Biomolecular Mass Spectrometry (BayBioMS), Technical University of Munich, Gregor-Mendel-Str. 4, 85354 Freising, Germany (1)
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Cell Signalling and Immunology, School of Life Sciences, University of Dundee, Dundee, UK (1)
Center for Cellular and Molecular Diagnostics, Department of Biochemistry and Molecular Biology, School of Medicine, Tulane University (1)
Copenhagen Center for Glycomics (CCG), Glyco-MS Group Department of Cellular and Molecular Medicine University of Copenhagen (1)
Department Willmitzer | Small-Molecule Signaling Max-Planck-Institut für Molekulare Pflanzenphysiologie Wissenschaftspark Golm Am Mühlenberg 1 14476 Potsdam (1)
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Department of Medical Informatics and Statistics, BK21 Project, Asan Medical Center, Asan Institute for Life Sciences, University of Ulsan College of Medicine, 88 Olympic-ro 43-gil, Songpa-gu, Seoul 05505, Republic of Korea. (1)
Department of Molecular and Applied Microbiology, Leibniz Institute for Natural Product Research and Infection Biology - Hans Knöll Institute Jena (1)
Department of Urology, Department of Biochemistry and Molecular Biology, Cancer Research Institute, SUNY Upstate Medical University, 750 E. Adams St., Syracuse, NY 13210, USA (1)
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Evotec (1)
Friedrich Miescher Institute for Biomedical Research (FMI), Basel, Switzerland (1)
Head of Medical Microbiology and Immunology, Department of Health Science and Technology, Medical Faculty, Aalborg Universtity, Denmark (1)
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Institute of Biochemistry, Department of Biology, ETH Zurich, Zurich CH-8093, Switzerland (1)
Institute of Biochemistry, ETHZ (1)
Institute of Molecular Systems Biology, Department of Biology, ETH Zurich, Zurich, Switzerland (1)
Institute of Molecular Systems Biology, ETH Zurich (1)

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Biosafety and proteome profiles of distinct heat-inactivation methods for Mycobacterium tuberculosis

In this project, we investigated the effets of heat inactivation for different time points to evaluate the biosafety and proteome changes.

ORGANISM(S): Mycobacterium tuberculosis H37Rv

2022-06-09 | PXD027011 | Pride

Specimen Inactivation Methods for Proteomics – Comparisons of irradiation, chemical, and heat treatments on downstream serum analyses

Numerous studies have described the efficacy of heat inactivation, gamma irradiation, or treatment with guanidium-based chaotropic salts (e.g. TRIzol®) for pathogen inactivation of biological samples to ensure biosafety and biosecurity. However, the effect of these methods on the greater serum prote...

ORGANISM(S): Macaca mulatta (Rhesus macaque)

2025-10-13 | PXD062367 | Pride

Dia Inactivation Gamma irradiation Rhesus Serum Trizol Primate

Transcription profiling of recombinant E. coli to heat-shock and dual heat-shock recombinant protein induction

Recombinant Escherichia coli cultures are used to manufacture numerous therapeutic proteins and industrial enzymes, where many of these processes use elevated temperatures to induce recombinant protein production. The heat-shock response in wild-type E. coli has been well studied. In this study, t...

ORGANISM(S): Escherichia coli

2009-08-25 | E-GEOD-17507 | biostudies-arrayexpress

Heat inactivation of foetal bovine serum performed after EV-depletion influences the proteome of cell-derived extracellular vesicles

The release of extracellular vesicles (EVs) in cell cultures as well as their molecular cargo can be influenced by cell culture conditions such as the presence of foetal bovine serum (FBS). Although several studies have evaluated the effect of removing FBS-derived EVs by ultracentrifugation (UC), le...

ORGANISM(S): Bos taurus (Bovine)

2024-01-26 | PXD047505 | Pride

Ev depletion by ultracentrifugation Foetal bovine serum (fbs) Extracellular vesicles Fbs heat-inactivation

Heat shock experimental replicates

Heat stress experiments imposed on Buchnera aphidicola within intact Schizaphis graminum hosts. NOTE: normalized values in GEO are NOT those derived from intensive analyses described in paper. Please see Wilcox et al. 2002 for description. Keywords = reduced bacterial genome, stress response

ORGANISM(S): Buchnera aphidicola (Schizaphis graminum)

2003-01-20 | E-GEOD-87 | biostudies-arrayexpress

Tight coordination of protein translation and heat shock factor 1 activation supports the anabolic malignant state [ChIP-Seq]

A unifying characteristic of aggressive cancers is a profound anabolic shift in metabolism to enable sustained proliferation and biomass expansion. The ribosome is centrally situated to sense metabolic states but whether it impacts systems that promote cellular survival is unknown. Here, through ...

ORGANISM(S): Homo sapiens

2013-07-21 | E-GEOD-45852 | biostudies-arrayexpress

Heat inactivation of Nipah virus for downstream single cell RNA sequencing

PRJNA1037503 | ENA

Thermoring Basis for the Heat Inactivation in TRPV1.

Not available

S-EPMC10479453 | biostudies-literature

Transcriptional analysis of E. coli whole genome during heat inactivation processes related to industrial cooking

This study was conducted to determine the impact of extreme temperatures, aiming at controlling microorganisms by cooking, on the physiology and the transcriptome of Escherichia coli. ABSTRACT: Because the genome of Escherichia coli K12 is well understood, this organism was used as a model to inves...

ORGANISM(S): Escherichia coli str. K-12 substr. MG1655

2012-09-15 | E-GEOD-40557 | biostudies-arrayexpress

Biosafety and Proteome Profiles of Different Heat Inactivation Methods for Mycobacterium tuberculosis.

Not available

S-EPMC8694153 | biostudies-literature

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