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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    International journal of peptide research and therapeutics 4 (1997), S. 429-436 
    ISSN: 1573-3904
    Keywords: Membrane ; Tat ; Vectorization
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Tat, a 86-amino acid protein involved in the replication of Human Immunodeficiency Virus type 1 (HIV-1), is able to translocate efficiently through the plasma membrane and to reach the nucleus to transactivate the viral genome. The region 37–72 of the Tat protein, centered on a cluster of basic amino acids, has been assigned to this translocation activity. Recent data in our group have attributed this membrane translocating activity to a peptide extending from residues 48 to 60, which contains a cluster of eight basic amino acids within a linear sequence of nine residues. Internalization of this peptide into cells occurred within minutes at concentrations as low as 100 nM. In order to define more precisely the involvement of these basic amino acids in peptide translocation, several analogues carrying deletions or substitutions of one, or several, of the basic residues were synthesized and tested for their cellular uptake and nuclear translocation. A direct correlation between the overall charge of the peptide and its cell internalization was found. In addition, the covalent linkage of this short basic peptide allows the efficient translocation of a non-membrane permeant peptide.
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    International journal of peptide research and therapeutics 4 (1997), S. 429-436 
    ISSN: 1573-3904
    Keywords: Membrane ; Tat ; Vectorization
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Tat, a 86-amino acid protein involved in thereplication of Human Immunodeficiency Virus type 1(HIV-1), is able to translocate efficiently throughthe plasma membrane and to reach the nucleus totransactivate the viral genome. The region 37–72 ofthe Tat protein, centered on a cluster of basicamino acids, has been assigned to this translocationactivity. Recent data in our group have attributedthis membrane translocating activity to a peptideextending from residues 48 to 60, which contains acluster of eight basic amino acids within a linearsequence of nine residues. Internalization of thispeptide into cells occurred within minutes atconcentrations as low as 100 nM. In order to definemore precisely the involvement of these basic aminoacids in peptide translocation, several analoguescarrying deletions or substitutions of one, orseveral, of the basic residues were synthesized andtested for their cellular uptake and nucleartranslocation. A direct correlation between theoverall charge of the peptide and its cellinternalization was found. In addition, the covalentlinkage of this short basic peptide allows theefficient translocation of a non-membrane permeant peptide.
    Type of Medium: Electronic Resource
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  • 3
    Publication Date: 2014-09-19
    Description: Rapid industrialization and urbanization in developing countries has led to an increase in air pollution, along a similar trajectory to that previously experienced by the developed nations. In China, particulate pollution is a serious environmental problem that is influencing air quality, regional and global climates, and human health. In response to the extremely severe and persistent haze pollution experienced by about 800 million people during the first quarter of 2013 (refs 4, 5), the Chinese State Council announced its aim to reduce concentrations of PM2.5 (particulate matter with an aerodynamic diameter less than 2.5 micrometres) by up to 25 per cent relative to 2012 levels by 2017 (ref. 6). Such efforts however require elucidation of the factors governing the abundance and composition of PM2.5, which remain poorly constrained in China. Here we combine a comprehensive set of novel and state-of-the-art offline analytical approaches and statistical techniques to investigate the chemical nature and sources of particulate matter at urban locations in Beijing, Shanghai, Guangzhou and Xi'an during January 2013. We find that the severe haze pollution event was driven to a large extent by secondary aerosol formation, which contributed 30-77 per cent and 44-71 per cent (average for all four cities) of PM2.5 and of organic aerosol, respectively. On average, the contribution of secondary organic aerosol (SOA) and secondary inorganic aerosol (SIA) are found to be of similar importance (SOA/SIA ratios range from 0.6 to 1.4). Our results suggest that, in addition to mitigating primary particulate emissions, reducing the emissions of secondary aerosol precursors from, for example, fossil fuel combustion and biomass burning is likely to be important for controlling China's PM2.5 levels and for reducing the environmental, economic and health impacts resulting from particulate pollution.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Huang, Ru-Jin -- Zhang, Yanlin -- Bozzetti, Carlo -- Ho, Kin-Fai -- Cao, Jun-Ji -- Han, Yongming -- Daellenbach, Kaspar R -- Slowik, Jay G -- Platt, Stephen M -- Canonaco, Francesco -- Zotter, Peter -- Wolf, Robert -- Pieber, Simone M -- Bruns, Emily A -- Crippa, Monica -- Ciarelli, Giancarlo -- Piazzalunga, Andrea -- Schwikowski, Margit -- Abbaszade, Gulcin -- Schnelle-Kreis, Jurgen -- Zimmermann, Ralf -- An, Zhisheng -- Szidat, Sonke -- Baltensperger, Urs -- El Haddad, Imad -- Prevot, Andre S H -- England -- Nature. 2014 Oct 9;514(7521):218-22. doi: 10.1038/nature13774. Epub 2014 Sep 17.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉1] Laboratory of Atmospheric Chemistry, Paul Scherrer Institute (PSI), 5232 Villigen, Switzerland [2] State Key Laboratory of Loess and Quaternary Geology (SKLLQG), and Key Laboratory of Aerosol Chemistry and Physics, Institute of Earth Environment, Chinese Academy of Sciences, Xi'an 710075, China [3]. ; 1] Department of Chemistry and Biochemistry, and Oeschger Centre for Climate Change Research, University of Bern, 3012 Bern, Switzerland [2] Laboratory of Radiochemistry and Environmental Chemistry, Paul Scherrer Institute (PSI), 5232 Villigen, Switzerland. ; Laboratory of Atmospheric Chemistry, Paul Scherrer Institute (PSI), 5232 Villigen, Switzerland. ; The Jockey Club School of Public Health and Primary Care, The Chinese University of Hong Kong, Hong Kong, China. ; State Key Laboratory of Loess and Quaternary Geology (SKLLQG), and Key Laboratory of Aerosol Chemistry and Physics, Institute of Earth Environment, Chinese Academy of Sciences, Xi'an 710075, China. ; 1] Laboratory of Atmospheric Chemistry, Paul Scherrer Institute (PSI), 5232 Villigen, Switzerland [2] European Commission, Joint Research Centre, Institute for Environment and Sustainability, Air and Climate Unit, Via Fermi, 2749, 21027 Ispra, Italy. ; Department of Earth and Environmental Sciences, University of Milano Bicocca, Piazza della Scienza 1, Milan 20126, Italy. ; Helmholtz Zentrum Munchen, German Research Center for Environmental Health (GmbH), Joint Mass Spectrometry Centre, Cooperation Group Comprehensive Molecular Analytics and Helmholtz Virtual Institute of Complex Molecular Systems in Environmental Health - Aerosol and Health (HICE), 85764 Neuherberg, Germany. ; 1] Helmholtz Zentrum Munchen, German Research Center for Environmental Health (GmbH), Joint Mass Spectrometry Centre, Cooperation Group Comprehensive Molecular Analytics and Helmholtz Virtual Institute of Complex Molecular Systems in Environmental Health - Aerosol and Health (HICE), 85764 Neuherberg, Germany [2] University of Rostock, Joint Mass Spectrometry Centre, Institute of Chemistry, Analytical Chemistry, 18015 Rostock, Germany. ; Department of Chemistry and Biochemistry, and Oeschger Centre for Climate Change Research, University of Bern, 3012 Bern, Switzerland. ; 1] Laboratory of Atmospheric Chemistry, Paul Scherrer Institute (PSI), 5232 Villigen, Switzerland [2].〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/25231863" target="_blank"〉PubMed〈/a〉
    Keywords: Aerosols/*analysis/chemistry ; Air Pollutants/*analysis/*chemistry ; Air Pollution/*analysis ; Biomass ; China ; Cities ; Environmental Monitoring ; Fossil Fuels ; Humans ; Organic Chemicals/analysis/chemistry ; Particulate Matter/*analysis/*chemistry ; Public Health ; Volatile Organic Compounds/analysis/chemistry
    Print ISSN: 0028-0836
    Electronic ISSN: 1476-4687
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
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  • 4
    Publication Date: 1987-07-24
    Description: Neuronal cells express a pp60c-src variant that displays an altered electrophoretic mobility and a different V8 peptide pattern relative to pp60c-src expressed in tissues of non-neuronal origin. To determine whether the neuronal form of pp60c-src is encoded by a brain-specific messenger RNA, a mouse brain complementary DNA (cDNA) library was screened with a chicken c-src probe and a 3.8-kilobase c-src cDNA clone was isolated. This clone encodes a 60-kilodalton protein that differs from chicken or human pp60c-src primarily in having six extra amino acids (Arg-Lys-Val-Asp-Val-Arg) within the NH2-terminal 16 kilodaltons of the molecule. S1 nuclease protection analysis confirmed that brain c-src RNA contains an 18-nucleotide insertion at the position of the extra six amino acids. This insertion occurs at a position that corresponds to a splice junction in the chicken and human c-src genes. The isolated c-src cDNA clone encodes a protein that displays an identical V8 peptide pattern to that observed in pp60c-src isolated from tissues of neuronal origin.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Martinez, R -- Mathey-Prevot, B -- Bernards, A -- Baltimore, D -- P0I CA38497/CA/NCI NIH HHS/ -- New York, N.Y. -- Science. 1987 Jul 24;237(4813):411-5.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/2440106" target="_blank"〉PubMed〈/a〉
    Keywords: Amino Acid Sequence ; Animals ; Base Sequence ; Brain/enzymology ; Chickens ; Cloning, Molecular ; DNA/metabolism ; DNA Restriction Enzymes ; DNA Transposable Elements ; Humans ; Isoenzymes/*genetics ; Mice ; Neurons/*enzymology ; Protein Kinases/*genetics ; Proto-Oncogene Proteins/*genetics ; Proto-Oncogene Proteins pp60(c-src) ; Sequence Homology, Nucleic Acid ; Species Specificity
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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