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Yue Ju

Researcher at Ohio State University

Publications -  9
Citations -  196

Yue Ju is an academic researcher from Ohio State University. The author has contributed to research in topics: Mass spectrometry & Protein subunit. The author has an hindex of 6, co-authored 8 publications receiving 154 citations. Previous affiliations of Yue Ju include Bruker.

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Paper Spray Ionization of Noncovalent Protein Complexes

TL;DR: This is the first report to show that PS ionization is a promising ionization method for nonconvalent protein complexes and it is possible to detect hemoglobin tetramer from a blood sample with minimal sample preparation.
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Relative interfacial cleavage energetics of protein complexes revealed by surface collisions.

TL;DR: It is demonstrated that dissociation of protein complexes by surface collisions, at the lower end of the typical surface-induced dissociation (SID) collision energy range, consistently cleaves the weakest protein:protein interfaces, producing products that are reflective of the known structure.
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Localization of Protein Complex Bound Ligands by Surface-Induced Dissociation High-Resolution Mass Spectrometry.

TL;DR: The suitability of SID to locate the ligand binding sites in protein complexes to study C-reactive protein pentamer and cholera toxin B has potential application in localizing sites of small ligandbinding for multisubunit protein-ligand complexes.
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Structural Characterization and Disulfide Assignment of Spider Peptide Phα1β by Mass Spectrometry

TL;DR: In this article, the authors used biochemical and mass spectrometry approaches to determine the disulfide linkages present in the recombinant Phα1β peptide, which has been shown to have an extensive analgesic effect with fewer side effects than ω-conotoxin MVIIA.
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The Pseudomonas aeruginosa AmrZ C-terminal domain mediates tetramerization and is required for its activator and repressor functions.

TL;DR: It is demonstrated that the primary AmrZ form in solution is tetrameric, and the C-terminal domain is essential for efficient AmRZ-mediated activation and repression of its targets.