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Starling, T.

Publications and source records attributed to Starling, T..

4 recordsLinked to original sources

Female behavioral cues control male courtship plasticity independent of female pheromones in African Drosophila melanogaster

Sexual interactions involve the exchange of information-including olfactory, auditory, and visual cues-that has been shaped by sexual selection to maximize fitness. While these courtship signals and behaviors are often characterized as stereotypical and species-specific, male courtship is plastic and can depend on the population identity of the courted female. The ability of a male to adjust his courtship behavior based on female identity has significant implications for how selection operates on courtship, potentially driving behavioral divergence between populations and the eventual emergence of new species. A major challenge is identifying the cues that males use to adjust their courtship strategy. We used Drosophila melanogaster to investigate the mechanisms facilitating courtship plasticity, focusing on male song production. Male song is often considered the paramount behavior performed by males and is stimulated by female pheromones. Previous observations have focused on cosmopolitan (non-African) genotypes, whereas the singing rate and singing plasticity is highly variable in African populations. In genotypes from Zimbabwe, females have a different major pheromone compound (5,9-HD) compared to non-African females and show strong behavioral preference for Zimbabwe males. We created a Zimbabwe genotype lacking 5,9-HD by disrupting the gene desat2 in the Zimbabwe Z53 strain. We tested the hypothesis that Zimbabwe male courtship plasticity depends on female pheromones by allowing males to court non-African, wild type Z53, and Z53 desat2 null mutant females. We found that males treated Z53 desat2 null females like wild type Z53 females, not using pheromone cues to determine singing and courtship plasticity. This suggests that other female behavioral feedback influences singing plasticity. This courtship plasticity could contribute to the asymmetrical reproductive isolation between these populations and could provide insight to the broad pattern of asymmetrical reproductive isolation across broad taxonomic groups.

evolutionary biology↗

Early HIV-1 maturation drives Env clustering and fusion competence

Human immunodeficiency virus type 1 (HIV-1) particles are initially released from the cell in an immature state that cannot cause infection. The proteolytic processing of the Gag structural polyprotein into its individual components triggers a dramatic structural reorganisation that produces fully mature and infectious virions. HIV-1 maturation remodels the Gag lattice to enable membrane fusion, but how early proteolytic steps regulate the envelope glycoprotein (Env) organisation is unknown. Although cryo-electron tomography has defined structural intermediates of maturation, it has not resolved how Env conformers relate to specific early maturation states. Here, we show that partial Gag cleavage, prior to capsid formation, allosterically reorganises the membrane-proximal lattice, promoting Env clustering and fusion-competent conformations. Using native virus preparations combined with cryogenic fluorescence-lifetime imaging correlated to cryo-electron tomography, we map Env conformational signatures onto defined Gag-processing intermediates. This reveals an unrecognised early maturation stage in which incomplete Gag processing primes Env for entry, shifting current models by positioning functional Env activation upstream of core maturation. These results establish that early lattice remodelling is a key determinant of HIV-1 fusion competence and expose a previously inaccessible, intervention-sensitive step with implications for therapeutic and vaccine strategies targeting maturation-entry coupling.

microbiology↗

Alpha-BET: Functional labeling of envelope glycoproteins with single domain antibodies for in-virus single molecule imaging

We present Alpha-BET, a structure-guided strategy leveraging AlphaFold to identify optimal ALFA-tag insertion sites for minimally disruptive labeling of viral glycoproteins with high-affinity nanobodies. Applied to HIV-1 Env, SARS-CoV-2 S, and NiV G, Alpha-BET preserves structural integrity and function. For HIV-1 Env, we demonstrate super-resolution DNA-PAINT MINFLUX 3D imaging enabled by tag insertion, showcasing its power for visualizing native trimers in single virions and potential for broader applications in virus research.

biophysics↗

Live Cell Multicolour Lifetime Imaging Using Genetically Encodable Fluorophores

Nine fluorescent proteins (FPs) simultaneous imaging has been demonstrated in a single acquisition using fluorescence lifetime imaging microscopy (FLIM) combined with pulsed interleaved excitation (PIE) for three laser lines. We also show how to unmix spectrally similar FPs in a pixel-by-pixel manner with an analytical non-fitting solution.

biophysics↗