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Institución detectada Período Navegá Descargá Solicitá
No detectada desde mar. 1997 / hasta dic. 2023 Science Journals

Información

Tipo de recurso:

revistas

ISSN impreso

0036-8075

ISSN electrónico

1095-9203

Editor responsable

American Association for the Advancement of Science (AAAS)

País de edición

Estados Unidos

Fecha de publicación

Cobertura temática

Tabla de contenidos

Rewiring the adolescent brain

Caroline Ash; Jesse Smith (eds.)

Palabras clave: Multidisciplinary.

Pp. 996.3-997

Imaging out-of-sight objects

Caroline Ash; Jesse Smith (eds.)

Palabras clave: Multidisciplinary.

Pp. 996.4-997

Sourcing brain abnormality

Caroline Ash; Jesse Smith (eds.)

Palabras clave: Multidisciplinary.

Pp. 996.5-997

Asteroid dynamics inside Venus' orbit

Caroline Ash; Jesse Smith (eds.)

Palabras clave: Multidisciplinary.

Pp. 996.6-997

A wobbly nucleus

Caroline Ash; Jesse Smith (eds.)

Palabras clave: Multidisciplinary.

Pp. 996.7-997

Pectin homogalacturonan nanofilament expansion drives morphogenesis in plant epidermal cells

Kalina T. HaasORCID; Raymond Wightman; Elliot M. MeyerowitzORCID; Alexis PeaucelleORCID

<jats:title>Wavy walls built by nanofilaments</jats:title> <jats:p> In the model plant <jats:italic>Arabidopsis</jats:italic> , pavement cells fit together with the lobes and curves of jigsaw puzzle pieces. Such complex cell shapes, in plants, were generally thought to be driven by turgor pressure. Haas <jats:italic>et al.</jats:italic> now show that the extracellular cell wall can actively shape the cell it contains without relying on turgor pressure. Nanofilaments of pectin homogalacturonan in the cell wall shift between crystalline and anisotropic phases according to whether they are methylated. The shift in form drives changes in cell wall shape that stand independent of turgor pressure. </jats:p> <jats:p> <jats:italic>Science</jats:italic> , this issue p. <jats:related-article xmlns:xlink="http://www.w3.org/1999/xlink" ext-link-type="doi" issue="6481" page="1003" related-article-type="in-this-issue" vol="367" xlink:href="10.1126/science.aaz5103">1003</jats:related-article> </jats:p>

Palabras clave: Multidisciplinary.

Pp. 1003-1007

Structure of the secretory immunoglobulin A core

Nikit KumarORCID; Christopher P. ArthurORCID; Claudio CiferriORCID; Marissa L. MatsumotoORCID

<jats:title>Hefty structures of IgA and IgM complexes</jats:title> <jats:p> Immunoglobulin M (IgM) and IgA are antibody isotypes that can form higher-order secretory complexes (sIgM and sIgA), which allows them to effectively bind and neutralize antigens with low-affinity repetitive epitopes, such as those found on the surface of many bacteria and viruses. The assembly and transport of these molecules is also dependent on the joining chain (J-chain) and the polymeric immunoglobulin receptor (pIgR) secretory component (SC). The architecture of these complex, multimeric structures has remained elusive. Li <jats:italic>et al.</jats:italic> resolved cryo–electron microscopy structures of the sIgM-Fc pentamer in complex with the J-chain and SC. Using similar techniques, Kumar <jats:italic>et al.</jats:italic> visualized dimeric, tetrameric, and pentameric structures of secretory sIgA-Fc interacting with the J-chain and SC. Both groups report highly similar mechanisms wherein the J-chain serves as a template for antibody oligomerization. An unanticipated, amyloid-like assembly of the oligomerized structure is present in both cases, with the J-chain conferring asymmetry for pIgR binding and transcytosis. These studies may inform structure-based engineering of these molecules for future therapeutic purposes. </jats:p> <jats:p> <jats:italic>Science</jats:italic> , this issue p. <jats:related-article xmlns:xlink="http://www.w3.org/1999/xlink" ext-link-type="doi" issue="6481" page="1014" related-article-type="in-this-issue" vol="367" xlink:href="10.1126/science.aaz5425">1014</jats:related-article> , p. <jats:related-article xmlns:xlink="http://www.w3.org/1999/xlink" ext-link-type="doi" issue="6481" page="1008" related-article-type="in-this-issue" vol="367" xlink:href="10.1126/science.aaz5807">1008</jats:related-article> </jats:p>

Palabras clave: Multidisciplinary.

Pp. 1008-1014

Structural insights into immunoglobulin M

Yaxin LiORCID; Guopeng WangORCID; Ningning LiORCID; Yuxin WangORCID; Qinyu ZhuORCID; Huarui Chu; Wenjun Wu; Ying TanORCID; Feng Yu; Xiao-Dong Su; Ning Gao; Junyu XiaoORCID

<jats:title>Hefty structures of IgA and IgM complexes</jats:title> <jats:p> Immunoglobulin M (IgM) and IgA are antibody isotypes that can form higher-order secretory complexes (sIgM and sIgA), which allows them to effectively bind and neutralize antigens with low-affinity repetitive epitopes, such as those found on the surface of many bacteria and viruses. The assembly and transport of these molecules is also dependent on the joining chain (J-chain) and the polymeric immunoglobulin receptor (pIgR) secretory component (SC). The architecture of these complex, multimeric structures has remained elusive. Li <jats:italic>et al.</jats:italic> resolved cryo–electron microscopy structures of the sIgM-Fc pentamer in complex with the J-chain and SC. Using similar techniques, Kumar <jats:italic>et al.</jats:italic> visualized dimeric, tetrameric, and pentameric structures of secretory sIgA-Fc interacting with the J-chain and SC. Both groups report highly similar mechanisms wherein the J-chain serves as a template for antibody oligomerization. An unanticipated, amyloid-like assembly of the oligomerized structure is present in both cases, with the J-chain conferring asymmetry for pIgR binding and transcytosis. These studies may inform structure-based engineering of these molecules for future therapeutic purposes. </jats:p> <jats:p> <jats:italic>Science</jats:italic> , this issue p. <jats:related-article xmlns:xlink="http://www.w3.org/1999/xlink" ext-link-type="doi" issue="6481" page="1014" related-article-type="in-this-issue" vol="367" xlink:href="10.1126/science.aaz5425">1014</jats:related-article> , p. <jats:related-article xmlns:xlink="http://www.w3.org/1999/xlink" ext-link-type="doi" issue="6481" page="1008" related-article-type="in-this-issue" vol="367" xlink:href="10.1126/science.aaz5807">1008</jats:related-article> </jats:p>

Palabras clave: Multidisciplinary.

Pp. 1014-1017

Ultrafast control of vortex microlasers

Can HuangORCID; Chen Zhang; Shumin XiaoORCID; Yuhan WangORCID; Yubin FanORCID; Yilin Liu; Nan ZhangORCID; Geyang QuORCID; Hongjun JiORCID; Jiecai Han; Li GeORCID; Yuri KivsharORCID; Qinghai SongORCID

<jats:title>Ultrafast vortex microlasers</jats:title> <jats:p> For applications in ultrafast communication, all-optical switches will require low energy consumption, high speed, a strong modulation ratio, a small footprint, and on-chip integration. Although the small footprint and on-chip integration are accessible, the trade-off between low energy consumption and high speed has been challenging. Huang <jats:italic>et al.</jats:italic> exploited the idea of bound states in the continuum, effectively a high–quality ( <jats:italic>Q</jats:italic> ) cavity without the physical cavity, to design vortex lasers with highly directional output and single-mode operation. With the trade-off between low energy consumption and high speed now broken, it should be possible to realize ultrafast optical switching that meets all the requirements of modern classic and quantum information. </jats:p> <jats:p> <jats:italic>Science</jats:italic> , this issue p. <jats:related-article xmlns:xlink="http://www.w3.org/1999/xlink" ext-link-type="doi" issue="6481" page="1018" related-article-type="in-this-issue" vol="367" xlink:href="10.1126/science.aba4597">1018</jats:related-article> </jats:p>

Palabras clave: Multidisciplinary.

Pp. 1018-1021

Aminoalkyl radicals as halogen-atom transfer agents for activation of alkyl and aryl halides

Timothée ConstantinORCID; Margherita Zanini; Alessio RegniORCID; Nadeem S. SheikhORCID; Fabio JuliáORCID; Daniele LeonoriORCID

<jats:title>Amines as a gateway to alkyl radicals</jats:title> <jats:p> In recent years, photoredox catalysis driven by blue light has often been used to oxidize carbon centers adjacent to nitrogen. Constantin <jats:italic>et al.</jats:italic> now show that these aminoalkyl radicals can, in turn, conveniently strip iodine atoms from a variety of alkyl carbons. The new alkyl radicals that result readily undergo deuteration and couplings such as alkylation, allylation, and olefination. The upshot is that simple amines can replace more hazardous conventional reagents such as trialkyltin compounds in the homolytic activation and functionalization of halocarbons. </jats:p> <jats:p> <jats:italic>Science</jats:italic> , this issue p. <jats:related-article xmlns:xlink="http://www.w3.org/1999/xlink" ext-link-type="doi" issue="6481" page="1021" related-article-type="in-this-issue" vol="367" xlink:href="10.1126/science.aba2419">1021</jats:related-article> </jats:p>

Palabras clave: Multidisciplinary.

Pp. 1021-1026