Enhancement of intracellular concentration and biological activity of PNA after conjugation with a cell-penetrating synthetic model peptide

European Journal of Biochemistry

Volumn 271, Issue 14, 2004, Pages 3043-3049

  Oehlke, Johannes ^a   Wallukat, Gerd ^b   Wolf, Yvonne ^a   Ehrlich, Angelika ^a   Wiesner, Burkhard ^a   Berger, Hartmut ^a   Bienert, Michael ^a  

^a LEIBNIZ INSTITUT FÜR MOLEKULARE PHARMAKOLOGIE   (Germany)

^b MAX DELBRÜCK CENTER FOR MOLECULAR MEDICINE   (Germany)

Author keywords

Cell penetrating peptides; Cellular uptake; PNA peptide conjugates

Indexed keywords

FLUORESCEIN; MESSENGER RNA; NEUROPEPTIDE; NOCICEPTIN; NOCICEPTIN RECEPTOR; PEPTIDE NUCLEIC ACID;

ALPHA HELIX; ANIMAL CELL; ARTICLE; BIOAVAILABILITY; CAPILLARY ELECTROPHORESIS; CELL LABELING; CELL SELECTION; CHO CELL; CHRONOTROPISM; CONJUGATION; CONTROLLED STUDY; COVALENT BOND; FEMALE; HEART MUSCLE CELL; INTRACELLULAR MEMBRANE; LASER; MAMMAL CELL; MODEL; NONHUMAN; PRIORITY JOURNAL; RAT;

AMINO ACID SEQUENCE; ANIMALS; ANIMALS, NEWBORN; BASE SEQUENCE; BIOLOGICAL TRANSPORT; CELLS, CULTURED; CHO CELLS; CRICETINAE; ENDOCYTOSIS; HUMANS; MYOCYTES, CARDIAC; OPIOID PEPTIDES; PEPTIDE NUCLEIC ACIDS; PEPTIDES; RATS; RATS, SPRAGUE-DAWLEY; RECEPTORS, OPIOID; RNA, MESSENGER;

ANIMALIA; MAMMALIA;

EID: 3242798141     PISSN: 00142956     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1432-1033.2004.04236.x     Document Type: Article

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