Angewandte Chemie (Weinheim an der Bergstrasse, Germany)最新文献

筛选
英文 中文
Probing the Lipid Annular Belt by Gas-Phase Dissociation of Membrane Proteins in Nanodiscs. 纳米圆盘膜蛋白气相解离探测脂质环状带。
Angewandte Chemie (Weinheim an der Bergstrasse, Germany) Pub Date : 2016-01-11 Epub Date: 2015-11-23 DOI: 10.1002/ange.201508289
Michael T Marty, Kin Kuan Hoi, Joseph Gault, Carol V Robinson
{"title":"Probing the Lipid Annular Belt by Gas-Phase Dissociation of Membrane Proteins in Nanodiscs.","authors":"Michael T Marty,&nbsp;Kin Kuan Hoi,&nbsp;Joseph Gault,&nbsp;Carol V Robinson","doi":"10.1002/ange.201508289","DOIUrl":"https://doi.org/10.1002/ange.201508289","url":null,"abstract":"<p><p>Interactions between membrane proteins and lipids are often crucial for structure and function yet difficult to define because of their dynamic and heterogeneous nature. Here, we use mass spectrometry to demonstrate that membrane protein oligomers ejected from nanodiscs in the gas phase retain large numbers of lipid interactions. The complex mass spectra that result from gas-phase dissociation were assigned using a Bayesian deconvolution algorithm together with mass defect analysis, allowing us to count individual lipid molecules bound to membrane proteins. Comparison of the lipid distributions measured by mass spectrometry with molecular dynamics simulations reveals that the distributions correspond to distinct lipid shells that vary according to the type of protein-lipid interactions. Our results demonstrate that nanodiscs offer the potential for native mass spectrometry to probe interactions between membrane proteins and the wider lipid environment.</p>","PeriodicalId":72198,"journal":{"name":"Angewandte Chemie (Weinheim an der Bergstrasse, Germany)","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2016-01-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/ange.201508289","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"36665186","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 7
Enzymology of Pyran Ring A Formation in Salinomycin Biosynthesis. 盐霉素生物合成中吡喃环A形成的酶学研究。
Angewandte Chemie (Weinheim an der Bergstrasse, Germany) Pub Date : 2015-11-09 Epub Date: 2015-09-17 DOI: 10.1002/ange.201507090
Hanna Luhavaya, Marcio V B Dias, Simon R Williams, Hui Hong, Luciana G de Oliveira, Peter F Leadlay
{"title":"Enzymology of Pyran Ring A Formation in Salinomycin Biosynthesis.","authors":"Hanna Luhavaya,&nbsp;Marcio V B Dias,&nbsp;Simon R Williams,&nbsp;Hui Hong,&nbsp;Luciana G de Oliveira,&nbsp;Peter F Leadlay","doi":"10.1002/ange.201507090","DOIUrl":"https://doi.org/10.1002/ange.201507090","url":null,"abstract":"<p><p>Tetrahydropyran rings are a common feature of complex polyketide natural products, but much remains to be learned about the enzymology of their formation. The enzyme SalBIII from the salinomycin biosynthetic pathway resembles other polyether epoxide hydrolases/cyclases of the MonB family, but SalBIII plays no role in the conventional cascade of ring opening/closing. Mutation in the <i>salBIII</i> gene gave a metabolite in which ring A is not formed. Using this metabolite in vitro as a substrate analogue, SalBIII has been shown to form pyran ring A. We have determined the X-ray crystal structure of SalBIII, and structure-guided mutagenesis of putative active-site residues has identified Asp38 and Asp104 as an essential catalytic dyad. The demonstrated pyran synthase activity of SalBIII further extends the impressive catalytic versatility of α+β barrel fold proteins.</p>","PeriodicalId":72198,"journal":{"name":"Angewandte Chemie (Weinheim an der Bergstrasse, Germany)","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2015-11-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/ange.201507090","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"34411945","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 4
Ribosome Subunit Stapling for Orthogonal Translation in E.coli. 大肠杆菌正交翻译的核糖体亚基钉接。
Angewandte Chemie (Weinheim an der Bergstrasse, Germany) Pub Date : 2015-10-19 Epub Date: 2015-08-26 DOI: 10.1002/ange.201506311
Stephen D Fried, Wolfgang H Schmied, Chayasith Uttamapinant, Jason W Chin
{"title":"Ribosome Subunit Stapling for Orthogonal Translation in <i>E.</i>  <i>coli</i>.","authors":"Stephen D Fried,&nbsp;Wolfgang H Schmied,&nbsp;Chayasith Uttamapinant,&nbsp;Jason W Chin","doi":"10.1002/ange.201506311","DOIUrl":"https://doi.org/10.1002/ange.201506311","url":null,"abstract":"<p><p>The creation of orthogonal large and small ribosomal subunits, which interact with each other but not with endogenous ribosomal subunits, would extend our capacity to create new functions in the ribosome by making the large subunit evolvable. To this end, we rationally designed a ribosomal RNA that covalently links the ribosome subunits via an RNA staple. The stapled ribosome is directed to an orthogonal mRNA, allowing the introduction of mutations into the large subunit that reduce orthogonal translation, but have minimal effects on cell growth. Our approach provides a promising route towards orthogonal subunit association, which may enable the evolution of key functional centers in the large subunit, including the peptidyl-transferase center, for unnatural polymer synthesis in cells.</p>","PeriodicalId":72198,"journal":{"name":"Angewandte Chemie (Weinheim an der Bergstrasse, Germany)","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2015-10-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/ange.201506311","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"34343771","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 45
Formation of Ruthenium Carbenes by gem-Hydrogen Transfer to Internal Alkynes: Implications for Alkyne trans-Hydrogenation. 通过向内部炔烃转移gem-Hydrogen形成钌羰基:对炔烃反式氢化的影响。
Angewandte Chemie (Weinheim an der Bergstrasse, Germany) Pub Date : 2015-10-12 Epub Date: 2015-08-31 DOI: 10.1002/ange.201506075
Markus Leutzsch, Larry M Wolf, Puneet Gupta, Michael Fuchs, Walter Thiel, Christophe Farès, Alois Fürstner
{"title":"Formation of Ruthenium Carbenes by <i>gem</i>-Hydrogen Transfer to Internal Alkynes: Implications for Alkyne <i>trans</i>-Hydrogenation.","authors":"Markus Leutzsch, Larry M Wolf, Puneet Gupta, Michael Fuchs, Walter Thiel, Christophe Farès, Alois Fürstner","doi":"10.1002/ange.201506075","DOIUrl":"10.1002/ange.201506075","url":null,"abstract":"<p><p>Insights into the mechanism of the unusual <i>trans</i>-hydrogenation of internal alkynes catalyzed by {Cp*Ru} complexes were gained by para-hydrogen (p-H<sub>2</sub>) induced polarization (PHIP) transfer NMR spectroscopy. It was found that the productive <i>trans</i>-reduction competes with a pathway in which both H atoms of H<sub>2</sub> are delivered to a single alkyne C atom of the substrate while the second alkyne C atom is converted into a metal carbene. This \"<i>geminal</i> hydrogenation\" mode seems unprecedented; it was independently confirmed by the isolation and structural characterization of a ruthenium carbene complex stabilized by secondary inter-ligand interactions. A detailed DFT study shows that the <i>trans</i> alkene and the carbene complex originate from a common metallacyclopropene intermediate. Furthermore, the computational analysis and the PHIP NMR data concur in that the metal carbene is the major gateway to olefin isomerization and over-reduction, which frequently interfere with regular alkyne <i>trans</i>-hydrogenation.</p>","PeriodicalId":72198,"journal":{"name":"Angewandte Chemie (Weinheim an der Bergstrasse, Germany)","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2015-10-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4955229/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"34331129","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
LP99: Discovery and Synthesis of the First Selective BRD7/9 Bromodomain Inhibitor. LP99:首个选择性BRD7/9溴域抑制剂的发现和合成。
Angewandte Chemie (Weinheim an der Bergstrasse, Germany) Pub Date : 2015-05-18 Epub Date: 2015-04-13 DOI: 10.1002/ange.201501394
Peter G K Clark, Lucas C C Vieira, Cynthia Tallant, Oleg Fedorov, Dean C Singleton, Catherine M Rogers, Octovia P Monteiro, James M Bennett, Roberta Baronio, Susanne Müller, Danette L Daniels, Jacqui Méndez, Stefan Knapp, Paul E Brennan, Darren J Dixon
{"title":"LP99: Discovery and Synthesis of the First Selective BRD7/9 Bromodomain Inhibitor.","authors":"Peter G K Clark,&nbsp;Lucas C C Vieira,&nbsp;Cynthia Tallant,&nbsp;Oleg Fedorov,&nbsp;Dean C Singleton,&nbsp;Catherine M Rogers,&nbsp;Octovia P Monteiro,&nbsp;James M Bennett,&nbsp;Roberta Baronio,&nbsp;Susanne Müller,&nbsp;Danette L Daniels,&nbsp;Jacqui Méndez,&nbsp;Stefan Knapp,&nbsp;Paul E Brennan,&nbsp;Darren J Dixon","doi":"10.1002/ange.201501394","DOIUrl":"https://doi.org/10.1002/ange.201501394","url":null,"abstract":"<p><p>The bromodomain-containing proteins BRD9 and BRD7 are part of the human SWI/SNF chromatin-remodeling complexes BAF and PBAF. To date, no selective inhibitor for BRD7/9 has been reported despite its potential value as a biological tool or as a lead for future therapeutics. The quinolone-fused lactam <b>LP99</b> is now reported as the first potent and selective inhibitor of the BRD7 and BRD9 bromodomains. Development of <b>LP99</b> from a fragment hit was expedited through balancing structure-based inhibitor design and biophysical characterization against tractable chemical synthesis: Complexity-building nitro-Mannich/lactamization cascade processes allowed for early structure-activity relationship studies whereas an enantioselective organocatalytic nitro-Mannich reaction enabled the synthesis of the lead scaffold in enantioenriched form and on scale. This epigenetic probe was shown to inhibit the association of BRD7 and BRD9 to acetylated histones in vitro and in cells. Moreover, <b>LP99</b> was used to demonstrate that BRD7/9 plays a role in regulating pro-inflammatory cytokine secretion.</p>","PeriodicalId":72198,"journal":{"name":"Angewandte Chemie (Weinheim an der Bergstrasse, Germany)","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2015-05-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/ange.201501394","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"34504120","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 148
Caterpillar Track Complexes in Template-Directed Synthesis and Correlated Molecular Motion. 模板指导合成和相关分子运动中的毛毛虫轨道复合物。
Angewandte Chemie (Weinheim an der Bergstrasse, Germany) Pub Date : 2015-04-27 Epub Date: 2015-02-12 DOI: 10.1002/ange.201412293
Shiqi Liu, Dmitry V Kondratuk, Sophie A L Rousseaux, Guzmán Gil-Ramírez, Melanie C O'Sullivan, Jonathan Cremers, Tim D W Claridge, Harry L Anderson
{"title":"Caterpillar Track Complexes in Template-Directed Synthesis and Correlated Molecular Motion.","authors":"Shiqi Liu, Dmitry V Kondratuk, Sophie A L Rousseaux, Guzmán Gil-Ramírez, Melanie C O'Sullivan, Jonathan Cremers, Tim D W Claridge, Harry L Anderson","doi":"10.1002/ange.201412293","DOIUrl":"10.1002/ange.201412293","url":null,"abstract":"<p><p>Small alterations to the structure of a star-shaped template totally change its mode of operation. The hexapyridyl template directs the conversion of a porphyrin dimer to the cyclic hexamer, but deleting one pyridine site changes the product to the cyclic decamer, while deleting two binding sites changes the product to the cyclic octamer. This surprising switch in selectivity is explained by the formation of 2:1 caterpillar track complexes, in which two template wheels bind inside the nanoring. Caterpillar track complexes can also be prepared by binding the hexapyridyl template inside the 8- and 10-porphyrin nanorings. NMR exchange spectroscopy (EXSY) experiments show that these complexes exhibit correlated motion, in which the conrotatory rotation of the two template wheels is coupled to rotation of the nanoring track. In the case of the 10-porphyrin system, the correlated motion can be locked by binding palladium(II) dichloride between the two templates.</p>","PeriodicalId":72198,"journal":{"name":"Angewandte Chemie (Weinheim an der Bergstrasse, Germany)","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2015-04-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4974918/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"34681776","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Biology and biochemistry of reproduction and contraception. 生殖和避孕的生物学和生物化学。
W JOCHLE
{"title":"Biology and biochemistry of reproduction and contraception.","authors":"W JOCHLE","doi":"","DOIUrl":"","url":null,"abstract":"","PeriodicalId":72198,"journal":{"name":"Angewandte Chemie (Weinheim an der Bergstrasse, Germany)","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"1962-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"23627273","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
相关产品
×
本文献相关产品
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信