What is she best known for?
The fields of study she is best known for:
- Enzyme
- Cell membrane
- Amino acid
Britta Brügger mainly investigates Cell biology, Biochemistry, Vesicle, Sphingomyelin and Golgi apparatus.
Britta Brügger incorporates Cell biology and Exosomal secretion in her studies.
Her Biochemistry research focuses on Infectivity and how it relates to Affinity chromatography, Glycoprotein, Hepatitis C virus and Viral shedding.
The concepts of her Vesicle study are interwoven with issues in Transport protein, Endoplasmic reticulum, Membrane transport and COPI.
Britta Brügger has researched Transport protein in several fields, including Vesicle-Associated Membrane Protein 2, Synaptic vesicle, Complexin and Neurotransmitter uptake.
Her biological study deals with issues like Membrane protein, which deal with fields such as Cell membrane, Membrane lipids, Lipid microdomain, Brefeldin A and Caveolin.
Her most cited work include:
- Ceramide Triggers Budding of Exosome Vesicles into Multivesicular Endosomes (1943 citations)
- Molecular Anatomy of a Trafficking Organelle (1648 citations)
- Quantitative analysis of biological membrane lipids at the low picomole level by nano-electrospray ionization tandem mass spectrometry. (746 citations)
What are the main themes of her work throughout her whole career to date?
Cell biology, Biochemistry, Golgi apparatus, Vesicle and COPI are her primary areas of study.
Her studies in Cell biology integrate themes in fields like Membrane and Membrane protein.
Her research on Membrane protein also deals with topics like
- Membrane lipids together with Sphingomyelin,
- Biological membrane that intertwine with fields like Protein–lipid interaction.
Her study in the field of Brefeldin A also crosses realms of Gene isoform.
Many of her studies on Vesicle apply to Transport protein as well.
Her COPI research is multidisciplinary, relying on both COP-Coated Vesicles, Vesicular transport protein, COPII, Coatomer and Coated vesicle.
She most often published in these fields:
- Cell biology (57.14%)
- Biochemistry (32.86%)
- Golgi apparatus (17.14%)
What were the highlights of her more recent work (between 2018-2021)?
- Cell biology (57.14%)
- Transmembrane protein (6.43%)
- Chromatography (7.14%)
In recent papers she was focusing on the following fields of study:
Her scientific interests lie mostly in Cell biology, Transmembrane protein, Chromatography, Mass spectrometry and Endoplasmic reticulum.
The Golgi apparatus and Sphingolipid research Britta Brügger does as part of her general Cell biology study is frequently linked to other disciplines of science, such as PINK1, therefore creating a link between diverse domains of science.
Britta Brügger studied Transmembrane protein and Transmembrane domain that intersect with Membrane protein, POPC and Vesicle.
Her Chromatography research is multidisciplinary, incorporating elements of Metabolite, Untargeted metabolomics, Glycerophospholipids and Lipidomics.
Her Mass spectrometry research integrates issues from Proteolysis, DNA and Trypsin.
Her Endoplasmic reticulum study combines topics from a wide range of disciplines, such as Calcium, Membrane biogenesis, Organelle and Transcriptional regulation.
Between 2018 and 2021, her most popular works were:
- CerS6-Derived Sphingolipids Interact with Mff and Promote Mitochondrial Fragmentation in Obesity. (54 citations)
- Quantification of phosphoinositides reveals strong enrichment of PIP2 in HIV-1 compared to producer cell membranes. (18 citations)
- Loss of Neurological Disease HSAN-I-Associated Gene SPTLC2 Impairs CD8+ T Cell Responses to Infection by Inhibiting T Cell Metabolic Fitness. (12 citations)
In her most recent research, the most cited papers focused on:
- Enzyme
- Cell membrane
- Amino acid
Britta Brügger mainly investigates Cell biology, Serine C-palmitoyltransferase, Immunology, mTORC1 and Inflammation.
Britta Brügger is involved in the study of Cell biology that focuses on Caveolae in particular.
Her research in Serine C-palmitoyltransferase intersects with topics in Unfolded protein response, Cytotoxic T cell and Intracellular.
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