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Darryl Johnson

Researcher at University of Georgia

Publications -  11
Citations -  576

Darryl Johnson is an academic researcher from University of Georgia. The author has contributed to research in topics: Cancer & Membrane protein. The author has an hindex of 10, co-authored 11 publications receiving 524 citations.

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Noctilisin, a Venom Glycopeptide of Sirex noctilio (Hymenoptera: Siricidae), Causes Needle Wilt and Defense Gene Responses in Pines.

TL;DR: A heat-stable factor that can migrate from the site of oviposition in the trunk through the xylem to needles in the crown of attacked pines was purified by size-fractionation and reversed-phase—high-performance liquid chromatography using activity assays based on defense gene induction as well as the needle wilt response in pine shoot explants.
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Optimization of data-dependent acquisition parameters for coupling high-speed separations with LC-MS/MS for protein identifications.

TL;DR: Optimize DDA settings were applied to the analysis of Trypanosome brucei peptides, yielding peptide identifications at a rate almost five times faster than previously used methodologies, which significantly improves protein identification workflows that use typical available instrumentation.
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Mitochondrial Membrane Complex That Contains Proteins Necessary for tRNA Import in Trypanosoma brucei

TL;DR: Results presented here identify and validate two novel protein components of the putative tRNA translocon and provide additional evidence that mitochondrial tRNA and protein import have shared components in trypanosomes.
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Carbon Fixation Driven by Molecular Hydrogen Results in Chemolithoautotrophically Enhanced Growth of Helicobacter pylori

TL;DR: Although this bacterium is already known to be highly adaptable to gastric niches, a new aspect of its metabolic flexibility, whereby molecular hydrogen use (energy) is coupled to carbon dioxide fixation (carbon acquisition) via a described carbon fixation enzyme, is shown here.
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The C-terminal fragment of axon guidance molecule Slit3 binds heparin and neutralizes heparin's anticoagulant activity.

TL;DR: Observations demonstrate that HSCF is a novel heparin-binding protein that potently neutralizes heParin's anticoagulation activity and reveals a potential for HSCf to be developed as a new antidote to treat overdosing of both hepar in and LMWH in clinical applications.