Catálogo de publicaciones - revistas

<jats:title>Gravitational interference</jats:title> <jats:p> The Aharonov-Bohm effect is a quantum mechanical effect in which a magnetic field affects the phase of an electron wave as it propagates along a wire. Atom interferometry exploits the wave characteristic of atoms to measure tiny differences in phase as they take different paths through the arms of an interferometer. Overstreet <jats:italic>et al</jats:italic> . split a cloud of cold rubidium atoms into two atomic wave packets about 25 centimeters apart and subjected one of the wave packets to gravitational interaction with a large mass (see the Perspective by Roura). The authors state that the observed phase shift is consistent with a gravitational Aharonov-Bohm effect. —ISO </jats:p>

<jats:p>A weekly roundup of information on newly offered instrumentation, apparatus, and laboratory materials of potential interest to researchers.</jats:p>

<jats:p>Darwin’s theory of sexual selection fundamentally changed how we think about sex and evolution. The struggle over mating and fertilization is a powerful driver of diversification within and among species. Contemporaries dismissed Darwin’s conjecture of a “taste for the beautiful” as favoring particular mates over others, but there is now overwhelming evidence for a primary role of both male and female mate choice in sexual selection. Darwin’s misogyny precluded much analysis of the “taste”; an increasing focus on mate choice mechanisms before, during, and after mating reveals that these often evolve in response to selection pressures that have little to do with sexual selection on chosen traits. Where traits and preferences do coevolve, they can do so whether fitness effects on choosers are positive, neutral, or negative. The spectrum of selection on traits and preferences, and how traits and preferences respond to social effects, determine how sexual selection and mate choice influence broader-scale processes like reproductive isolation and population responses to environmental change.</jats:p>

<jats:p> The analysis of dinosaur ecology hinges on the appropriate reconstruction and analysis of dinosaur biodiversity. Benson <jats:italic>et al</jats:italic> . question the data used in our analysis and our subsequent interpretation of the results. We address these concerns and show that their reanalysis is flawed. Indeed, when occurrences are filtered to include only valid taxa, their revised dataset strengthens our earlier conclusions. </jats:p>

<jats:p> Schroeder <jats:italic>et al</jats:italic> . (Reports, 26 February 2021, p. 941) reported a size gap among predatory dinosaur species. We argue that the supporting dataset is skewed toward Late Cretaceous North America and that the gap was likely absent during other intervals in most geographic regions. We urge broader consideration of this hypothesis, with quantitative evaluation of preservational and dataset biases. </jats:p>

<jats:p>Many studies have examined the impact of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variants on neutralizing antibody activity after they have become dominant strains. Here, we evaluate the consequences of further viral evolution. We demonstrate mechanisms through which the SARS-CoV-2 receptor binding domain (RBD) can tolerate large numbers of simultaneous antibody escape mutations and show that pseudotypes containing up to seven mutations, as opposed to the one to three found in previously studied variants of concern, are more resistant to neutralization by therapeutic antibodies and serum from vaccine recipients. We identify an antibody that binds the RBD core to neutralize pseudotypes for all tested variants but show that the RBD can acquire an N-linked glycan to escape neutralization. Our findings portend continued emergence of escape variants as SARS-CoV-2 adapts to humans.</jats:p>

<jats:p>Asymmetric multiprotein complexes that undergo subunit exchange play central roles in biology but present a challenge for design because the components must not only contain interfaces that enable reversible association but also be stable and well behaved in isolation. We use implicit negative design to generate β sheet–mediated heterodimers that can be assembled into a wide variety of complexes. The designs are stable, folded, and soluble in isolation and rapidly assemble upon mixing, and crystal structures are close to the computational models. We construct linearly arranged hetero-oligomers with up to six different components, branched hetero-oligomers, closed C4-symmetric two-component rings, and hetero-oligomers assembled on a cyclic homo-oligomeric central hub and demonstrate that such complexes can readily reconfigure through subunit exchange. Our approach provides a general route to designing asymmetric reconfigurable protein systems.</jats:p>

<jats:p>In multicellular organisms, gene regulatory circuits generate thousands of molecularly distinct, mitotically heritable states through the property of multistability. Designing synthetic multistable circuits would provide insight into natural cell fate control circuit architectures and would allow engineering of multicellular programs that require interactions among distinct cell types. We created MultiFate, a naturally inspired, synthetic circuit that supports long-term, controllable, and expandable multistability in mammalian cells. MultiFate uses engineered zinc finger transcription factors that transcriptionally self-activate as homodimers and mutually inhibit one another through heterodimerization. Using a model-based design, we engineered MultiFate circuits that generate as many as seven states, each stable for at least 18 days. MultiFate permits controlled state switching and modulation of state stability through external inputs and can be expanded with additional transcription factors. These results provide a foundation for engineering multicellular behaviors in mammalian cells.</jats:p>

<jats:p>As the Biden administration took office last January, with the pandemic peaking at more than 130,000 COVID-19 hospitalizations in the United States, there were high hopes for a new plan of “sticking to the science” and expectations that public health policies, communication, and trust would return to levels not seen for many years. That didn’t happen. Why?</jats:p>