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  • Polymer and Materials Science  (3)
  • Imaging, Three-Dimensional
  • 2005-2009  (2)
  • 1970-1974  (3)
  • 1
    Electronic Resource
    Electronic Resource
    Analysis of resorcinol-phenol-formaldehyde resins by NMR spectroscopy (1972)
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 26 (1972), S. 171-176 
    Details
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Es wird eine NMR-Methode zur Bestimmung der ungefähren Verhältnisse zwischen aus Phenolkernen, Resorcinkernen und Formaldehyd gebildeten Gruppenin Kondensationsprodukten aus Phenol, Resorcin und Formaldehyd beschrieben.
    Notes: A method is reported, based on NMR spectroscopy, for approximate determination of the component ratios of resins formed by condensation of resorcinol, phenol and formaldehyde.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/apmc.1972.050260113
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    Paper (German National Licenses)
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  • 2
    Electronic Resource
    Electronic Resource
    Paramagnetic shifts induced by europium and praseodymium chelates in the NMR spectrum of bisphenol a diglycidyl ether (1972)
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 27 (1972), S. 159-164 
    Details
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Es wurde eine Voruntersuchung des Einflusses unternommen, den die Verschiebereagenzien Tris-(dipivaloylmethano)-europium uncl Tris-(dipivaloylmethano)-pra-seodym auf das NMR-Spektrum des Diglyzidyläthers des Bisphenol A ausüben. Es ergab sich, daß die Signale der am Epoxidring anliegenden Protonen durch den Zusatz dieser Chelate weit mehr als die Signale der exozyklischen -OCH2-Gruppen verschoben werden. Die Verschiebung kann man durch den Zusatz eines Alkohols rückgängig machen, der vorzugsweise mit dem Verschiebemittel reagiert.
    Notes: A preliminary study has been made of the effects of the shift reagents Eu (DPM)3 and Pr(DPM)3 on the NMR spectrum of Bisphenol A diglycidyl ether (I). Protons attached to the epoxy ring were observed to shift appreciably more than protons of the exocyclic —OCH2— group, on addition of these chelates. The shifts could be reversed by addition of an alcohol, which interacted preferentially with the shift reagent.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/apmc.1972.050270111
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  • 3
    Electronic Resource
    Electronic Resource
    Paramagnetic shifts induced by europium and praseodymium complexes in the NMR spectra of some substituted phenols (1972)
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 27 (1972), S. 151-157 
    Details
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Es wurden die Verschiebungen untersucht, die durch Tris-(dipivaloylmethano)-europium und Tris-(dipivaloylmethano)-praseodym im NMR- Spektrum versehiedener Derivate substituierter Phenole hervorgerufen werden. Der Zweck dieser Arbeiten war, die Möglichkeiten zu erfassen, die diese Verschiebereagenzien als Hilfsmittel in der NMR-Analyse von Phenolharzen bieten, und Information über Verschiebungen bei Molekülen zu gewinnen, die mehr als eine Koordinationsposition besitzen.
    Notes: An investigation into the shifts induced in the NMR spectra of some derivatives of substituted phenols by tris(dipivalomethanato)europium and tris(dipivalomethanato)praseodymium is reported. The phenol derivatives were studied to ascertain the possible utility of the shift reagents as an aid in the analysis of phenolformaldehyde resins by NMR spectroscopy, and to gain information on induced shifts with molecules having more than one possible co-ordination site.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/apmc.1972.050270110
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  • 4
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    Self-assembly of a nanoscale DNA box with a controllable lid (2009)
    Nature Publishing Group (NPG)
    Details
    Publication Date: 2009-05-09
    Description: The unique structural motifs and self-recognition properties of DNA can be exploited to generate self-assembling DNA nanostructures of specific shapes using a 'bottom-up' approach. Several assembly strategies have been developed for building complex three-dimensional (3D) DNA nanostructures. Recently, the DNA 'origami' method was used to build two-dimensional addressable DNA structures of arbitrary shape that can be used as platforms to arrange nanomaterials with high precision and specificity. A long-term goal of this field has been to construct fully addressable 3D DNA nanostructures. Here we extend the DNA origami method into three dimensions by creating an addressable DNA box 42 x 36 x 36 nm(3) in size that can be opened in the presence of externally supplied DNA 'keys'. We thoroughly characterize the structure of this DNA box using cryogenic transmission electron microscopy, small-angle X-ray scattering and atomic force microscopy, and use fluorescence resonance energy transfer to optically monitor the opening of the lid. Controlled access to the interior compartment of this DNA nanocontainer could yield several interesting applications, for example as a logic sensor for multiple-sequence signals or for the controlled release of nanocargos.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Andersen, Ebbe S -- Dong, Mingdong -- Nielsen, Morten M -- Jahn, Kasper -- Subramani, Ramesh -- Mamdouh, Wael -- Golas, Monika M -- Sander, Bjoern -- Stark, Holger -- Oliveira, Cristiano L P -- Pedersen, Jan Skov -- Birkedal, Victoria -- Besenbacher, Flemming -- Gothelf, Kurt V -- Kjems, Jorgen -- England -- Nature. 2009 May 7;459(7243):73-6. doi: 10.1038/nature07971.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Danish National Research Foundation: Centre for DNA Nanotechnology.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/19424153" target="_blank"〉PubMed〈/a〉
    Keywords: Cryoelectron Microscopy ; DNA/*chemistry ; Imaging, Three-Dimensional ; Microscopy, Atomic Force ; Nanostructures/*chemistry ; *Nucleic Acid Conformation
    Print ISSN: 0028-0836
    Electronic ISSN: 1476-4687
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Published by Nature Publishing Group (NPG)
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  • 5
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    Structure of the anaphase-promoting complex/cyclosome interacting with a mitotic checkpoint complex (2009)
    American Association for the Advancement of Science (AAAS)
    Details
    Publication Date: 2009-03-17
    Description: Once all chromosomes are connected to the mitotic spindle (bioriented), anaphase is initiated by the protein ubiquitylation activity of the anaphase-promoting complex/cyclosome (APC/C) and its coactivator Cdc20 (APC/C(Cdc20)). Before chromosome biorientation, anaphase is delayed by a mitotic checkpoint complex (MCC) that inhibits APC/C(Cdc20). We used single-particle electron microscopy to obtain three-dimensional models of human APC/C in various functional states: bound to MCC, to Cdc20, or to neither (apo-APC/C). These experiments revealed that MCC associates with the Cdc20 binding site on APC/C, locks the otherwise flexible APC/C in a "closed" state, and prevents binding and ubiquitylation of a wide range of different APC/C substrates. These observations clarify the structural basis for the inhibition of APC/C by spindle checkpoint proteins.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2989460/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2989460/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Herzog, Franz -- Primorac, Ivana -- Dube, Prakash -- Lenart, Peter -- Sander, Bjorn -- Mechtler, Karl -- Stark, Holger -- Peters, Jan-Michael -- F 3407/Austrian Science Fund FWF/Austria -- New York, N.Y. -- Science. 2009 Mar 13;323(5920):1477-81. doi: 10.1126/science.1163300.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Research Institute of Molecular Pathology, Dr. Bohr-Gasse 7, 1030 Vienna, Austria.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/19286556" target="_blank"〉PubMed〈/a〉
    Keywords: Anaphase ; Anaphase-Promoting Complex-Cyclosome ; Cdc20 Proteins ; Cell Cycle Proteins/chemistry/metabolism ; HeLa Cells ; Humans ; Image Processing, Computer-Assisted ; Imaging, Three-Dimensional ; Microscopy, Electron ; *Mitosis ; Models, Molecular ; Protein Binding ; Protein Conformation ; Protein Structure, Tertiary ; Spindle Apparatus/*metabolism ; Ubiquitin-Conjugating Enzymes/chemistry/metabolism ; Ubiquitin-Protein Ligase Complexes/*chemistry/*metabolism ; Ubiquitination
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
    Published by American Association for the Advancement of Science (AAAS)
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