His primary areas of investigation include Biochemistry, Peptide, Peptide sequence, Molecular biology and Binding site. In general Biochemistry study, his work on Chaperone, Protein folding and Binding selectivity often relates to the realm of Sodium channel, thereby connecting several areas of interest. His Peptide study integrates concerns from other disciplines, such as Amino acid, Molecular recognition, Receptor, Membrane and Combinatorial chemistry.
His research integrates issues of Protein structure and Plasma protein binding in his study of Peptide sequence. His Molecular biology research incorporates elements of Tyrosine, JAK-STAT signaling pathway, Mutant, Epitope and Glycoprotein 130. The various areas that Jens Schneider-Mergener examines in his Binding site study include FKBP, Protein family, Solubilization and CLPB.
Jens Schneider-Mergener spends much of his time researching Peptide, Biochemistry, Epitope, Molecular biology and Amino acid. The Peptide study combines topics in areas such as Proteases, Membrane, Combinatorial chemistry, Peptide library and Linear epitope. His study looks at the relationship between Biochemistry and fields such as Cell biology, as well as how they intersect with chemical problems.
His Epitope research is multidisciplinary, relying on both Monoclonal antibody, Capsid and Virology. His biological study deals with issues like Antibody, which deal with fields such as Antigen and Cholera toxin. Protein domain and WW domain is closely connected to Stereochemistry in his research, which is encompassed under the umbrella topic of Amino acid.
His scientific interests lie mostly in Biochemistry, Peptide, Cell biology, Amino acid and Molecular biology. Jens Schneider-Mergener frequently studies issues relating to Biophysics and Biochemistry. Jens Schneider-Mergener usually deals with Peptide and limits it to topics linked to Protein ligand and Protein design, Ligation, Combinatorial chemistry and Spot synthesis.
His biological study spans a wide range of topics, including TIM/TOM complex, Membrane protein, Mitochondrial membrane transport protein, Transmembrane domain and Fungal protein. In his work, Peptoid, Bromoacetic acid, Membrane, Solid-phase synthesis and Enzyme is strongly intertwined with Stereochemistry, which is a subfield of Amino acid. His study looks at the intersection of Molecular biology and topics like Antibody with Cholera toxin.
Biochemistry, Protein domain, Chaperone, Peptide sequence and Computational biology are his primary areas of study. His Protein domain research includes elements of Protein structure, Affinities and Protein folding. His Chaperone research is multidisciplinary, incorporating elements of Biophysics, Substrate recognition, Mutational analysis and Binding site.
His studies deal with areas such as Polyproline helix, Ligand, Stereochemistry, Protein–protein interaction prediction and WW domain as well as Peptide sequence. Jens Schneider-Mergener has included themes like Protein–protein interaction, Human proteome project, SH3 domain, Phage display and Interactome in his Computational biology study. The study incorporates disciplines such as Proteome and Molecular recognition in addition to Protein–protein interaction.
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Substrate specificity of the DnaK chaperone determined by screening cellulose‐bound peptide libraries
Stefan Rüdiger;Lothar Germeroth;Jens Schneider‐Mergener;Bernd Bukau.
The EMBO Journal (1997)
Changing the antigen binding specificity by single point mutations of an anti-p24 (HIV-1) antibody.
Karsten Winkler;Achim Kramer;Gabriele Küttner;Martina Seifert.
Journal of Immunology (2000)
FAN, a Novel WD-Repeat Protein, Couples the p55 TNF-Receptor to Neutral Sphingomyelinase
Sabine Adam-Klages;Dieter Adam;Katja Wiegmann;Sandra Struve.
Differential Activation of Acute Phase Response Factor/STAT3 and STAT1 via the Cytoplasmic Domain of the Interleukin 6 Signal Transducer gp130 I. DEFINITION OF A NOVEL PHOSPHOTYROSINE MOTIF MEDIATING STAT1 ACTIVATION
Claudia Gerhartz;Birgit Heesel;Jürgen Sasse;Ulrike Hemmann.
Journal of Biological Chemistry (1996)
Target Structures of the CD8+-T-Cell Response to Human Cytomegalovirus: the 72-Kilodalton Major Immediate-Early Protein Revisited
Florian Kern;Ingolf Pascal Surel;Nicole Faulhaber;Claudia Frömmel.
Journal of Virology (1999)
Applications of peptide arrays prepared by the SPOT-technology.
Ulrich Reineke;Rudolf Volkmer-Engert;Jens Schneider-Mergener;Jens Schneider-Mergener.
Current Opinion in Biotechnology (2001)
T-CELL EPITOPE MAPPING BY FLOW CYTOMETRY
Florian Kern;Ingolf Pascal Surel;Carsten Brock;Bernd Freistedt.
Nature Medicine (1998)
Its substrate specificity characterizes the DnaJ co‐chaperone as a scanning factor for the DnaK chaperone
Stefan Rüdiger;Jens Schneider‐Mergener;Bernd Bukau.
The EMBO Journal (2001)
SHP2 and SOCS3 Contribute to Tyr-759-dependent Attenuation of Interleukin-6 Signaling through gp130
Ute Lehmann;Jochen Schmitz;Manuela Weissenbach;Radoslaw M. Sobota.
Journal of Biological Chemistry (2003)
Specific interactions between the syntrophin PDZ domain and voltage-gated sodium channels.
Johan Schultz;Ulrich Hoffmuüller;Gerd Krause;Jennifer Ashurst.
Nature Structural & Molecular Biology (1998)
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