Publications by authors named "W Alan Bradshaw"

Article Synopsis
  • Spleen tyrosine kinase (SYK) plays a crucial role in immune signaling and is kept inactive by its regulatory region which includes tandem SH2 domains connecting through a helical "hinge."
  • Activation of SYK occurs when these SH2 domains bind to phosphorylated motifs (ITAMs) on receptors, disrupting the hinge-kinase interaction, although the precise mechanism of this interaction has been unclear.
  • Recent studies involving crystal structures and mutational analyses have identified a conserved binding mechanism between phospho-ITAMs and the tSH2 domains, leading to structural changes that trigger SYK activation.
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The highly conserved and essential Plasmodium falciparum reticulocyte-binding protein homolog 5 (PfRH5) has emerged as the leading target for vaccines against the disease-causing blood stage of malaria. However, the features of the human vaccine-induced antibody response that confer highly potent inhibition of malaria parasite invasion into red blood cells are not well defined. Here, we characterize 236 human IgG monoclonal antibodies, derived from 15 donors, induced by the most advanced PfRH5 vaccine.

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RNA sequencing and genetic data support spleen tyrosine kinase (SYK) and high affinity immunoglobulin epsilon receptor subunit gamma (FCER1G) as putative targets to be modulated for Alzheimer's disease (AD) therapy. FCER1G is a component of Fc receptor complexes that contain an immunoreceptor tyrosine-based activation motif (ITAM). SYK interacts with the Fc receptor by binding to doubly phosphorylated ITAM (p-ITAM) via its two tandem SH2 domains (SYK-tSH2).

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SHIP1, an inositol 5-phosphatase, plays a central role in cellular signaling. As such, it has been implicated in many conditions. Exploiting SHIP1 as a drug target will require structural knowledge and the design of selective small molecules.

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We evaluated miRNA and mRNA expression differences in head tissues between avid-biting vs. reluctant-biting Aedes albopictus (Skuse) females from a single population over a 20-min timescale. We found no differences in miRNA expression between avid vs.

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