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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.
    Type of Medium: Electronic Resource
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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
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
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