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October 2010

HIV-1 Gag is the major structural protein that forms virus particles. In a majority of polarized T cells, Gag-YFP concentrates to a rear-end protrusion known as the uropod. As these uropods participate in cell-cell contacts with other cells, Gag accumulation to and virus assembly at uropods may facilitate virus spread. Consistent with this model, uropod components are observed at the virological synapses. Gag localization to uropods are driven by higher-order Gag multimerization dependent on the NC domain (see Llewellyn et al., doi:10.1371/journal.ppat.1001167).

Image Credit: G. Nicholas Llewellyn, University of Michigan Medical School

Opinion

Social Media and Microbiology Education

Vincent R. Racaniello

Pearls

Antimicrobial Peptides: Primeval Molecules or Future Drugs?

Brian M. Peters, Mark E. Shirtliff, Mary Ann Jabra-Rizk

Review

Host Genetics and HIV-1: The Final Phase?

Jacques Fellay, Kevin V. Shianna, Amalio Telenti, David B. Goldstein

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Fidelity Variants of RNA Dependent RNA Polymerases Uncover an Indirect, Mutagenic Activity of Amiloride Compounds

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The Spread of Tomato Yellow Leaf Curl Virus from the Middle East to the World

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Identification and Genome-Wide Prediction of DNA Binding Specificities for the ApiAP2 Family of Regulators from the Malaria Parasite

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