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Institution

Chinese Academy of Sciences

GovernmentBeijing, Beijing, China
About: Chinese Academy of Sciences is a government organization based out in Beijing, Beijing, China. It is known for research contribution in the topics: Catalysis & Population. The organization has 421602 authors who have published 634849 publications receiving 14894293 citations. The organization is also known as: CAS.
Topics: Catalysis, Population, Laser, Adsorption, Graphene


Papers
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Journal ArticleDOI
13 May 2020-Science
TL;DR: In isolation of four human-origin monoclonal antibodies from a convalescent patient, all of which display neutralization abilities, a therapeutic study in a mouse model validated that these antibodies can reduce virus titers in infected lungs.
Abstract: Neutralizing antibodies could potentially be used as antivirals against the coronavirus disease 2019 (COVID-19) pandemic. Here, we report isolation of four human-origin monoclonal antibodies from a convalescent patient, all of which display neutralization abilities. The antibodies B38 and H4 block binding between the spike glycoprotein receptor binding domain (RBD) of the virus and the cellular receptor angiotensin-converting enzyme 2 (ACE2). A competition assay indicated different epitopes on the RBD for these two antibodies, making them a potentially promising virus-targeting monoclonal antibody pair for avoiding immune escape in future clinical applications. Moreover, a therapeutic study in a mouse model validated that these antibodies can reduce virus titers in infected lungs. The RBD-B38 complex structure revealed that most residues on the epitope overlap with the RBD-ACE2 binding interface, explaining the blocking effect and neutralizing capacity. Our results highlight the promise of antibody-based therapeutics and provide a structural basis for rational vaccine design.

933 citations

Journal ArticleDOI
19 Feb 2010-Science
TL;DR: It is demonstrated that central metabolism enzymes in Salmonella were acetylated extensively and differentially in response to different carbon sources, concomitantly with changes in cell growth and metabolic flux.
Abstract: Lysine acetylation regulates many eukaryotic cellular processes, but its function in prokaryotes is largely unknown. We demonstrated that central metabolism enzymes in Salmonella were acetylated extensively and differentially in response to different carbon sources, concomitantly with changes in cell growth and metabolic flux. The relative activities of key enzymes controlling the direction of glycolysis versus gluconeogenesis and the branching between citrate cycle and glyoxylate bypass were all regulated by acetylation. This modulation is mainly controlled by a pair of lysine acetyltransferase and deacetylase, whose expressions are coordinated with growth status. Reversible acetylation of metabolic enzymes ensure that cells respond environmental changes via promptly sensing cellular energy status and flexibly altering reaction rates or directions. It represents a metabolic regulatory mechanism conserved from bacteria to mammals.

933 citations

Journal ArticleDOI
TL;DR: It is important to understand the current state of antibiotic use in China and its relationship to ARG prevalence and diversity in the environment, and also future needs in mitigating the spread of antibiotic resistance in the environments, particularly under the 'planetary health' perspective.

932 citations

Journal ArticleDOI
TL;DR: It is demonstrated that an l-proline or N,N-dimethylglycine ligand can facilitate most typical Ullmann-type reactions, with reactions occurring under relatively mild conditions and using only 2-20 mol % copper catalysts.
Abstract: Copper-assisted Ullmann-type coupling reactions are valuable transformations for organic synthesis. Researchers have extensively applied these reactions in both academic and industrial settings. However, two important issues, the high reaction temperatures (normally above 150 °C) and the stoichiometric amounts of copper necessary, have greatly limited the reaction scope. To solve these problems, we and other groups have recently explored the use of special ligands to promote these coupling reactions. We first showed that the structure of α-amino acids can accelerate Cu-assisted Ullmann reactions, leading to the coupling reactions of aryl halides and α-amino acids at 80−90 °C. In response to these encouraging results, we also discovered that an l-proline ligand facilitated the following transformations: (1) coupling of aryl halides with primary amines, cyclic secondary amines, and N-containing heterocycles at 40−90 °C; (2) coupling of aryl halides with sulfinic acid salts at 80−95 °C; (3) azidation of aryl...

932 citations

Journal ArticleDOI
TL;DR: In this article, a binary π-conjugated spacer of ethylenedioxythiophene and dithienosilole was used to construct a high molar absorption coefficient push−pull dye, characteristic of an intramolecular charge-transfer band peaking at 584 nm measured in chloroform.
Abstract: In view of the limited ruthenium resource, metal-free organic dyes may play a prominent role in the coming large-scale application of cost-effective dye-sensitized solar cells, if their efficiency and stability can be considerably improved. In this paper we utilized a binary π-conjugated spacer of ethylenedioxythiophene and dithienosilole to construct a high molar absorption coefficient push−pull dye, characteristic of an intramolecular charge-transfer band peaking at 584 nm measured in chloroform. In comparison with the standard ruthenium sensitizer Z907, this metal-free chromophore C219 endowed a nanocrystalline titania film with an evident light-harvesting enhancement, leading to an unprecedented 10.0−10.3% efficiency at the AM1.5G conditions for dye-sensitized solar cells with nonruthenium dyestuffs, although a highly volatile electrolyte was used. Transient absorption measurements have revealed that even if the kinetics of back-electron transfer and dye regeneration are considerably different for Z90...

932 citations


Authors

Showing all 422053 results

NameH-indexPapersCitations
Frank B. Hu2501675253464
Zhong Lin Wang2452529259003
Yi Chen2174342293080
Jing Wang1844046202769
Peidong Yang183562144351
Xiaohui Fan183878168522
H. S. Chen1792401178529
Douglas Scott1781111185229
Jie Zhang1784857221720
Pulickel M. Ajayan1761223136241
Feng Zhang1721278181865
Andrea Bocci1722402176461
Yang Yang1712644153049
Lei Jiang1702244135205
Yang Gao1682047146301
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
2023170
20222,918
202159,109
202055,057
201952,186
201846,329