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Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 9/2009, Volume 106, Issue 38, pp. 16157 - 16162
Screening of phage libraries expressing random peptides for binding to prostate cancer cells primarily yielded peptides that had a Cterminal arginine (or... 
Bacteriophages | Proteins | Receptors | Neurons | Internalization | Cell lines | Antibodies | Ligands | Endothelial cells | Tumors | Cell penetrating peptides | Vascular permeability | VEGF | Homing peptides | cell penetrating peptides | HEPARIN-BINDING | PROTEIN | PERMEABILITY FACTOR | ANGIOGENESIS | MULTIDISCIPLINARY SCIENCES | RECEPTOR | TUMOR-CELLS | SECRETE | HUMAN IMMUNODEFICIENCY VIRUS | homing peptides | vascular permeability | DOMAINS | ENDOTHELIAL GROWTH-FACTOR | Neuropilin-1 - genetics | Neoplasm Transplantation | Prostatic Neoplasms - metabolism | Neuropilin-1 - metabolism | Humans | Peptides - pharmacokinetics | Male | Transplantation, Heterologous | Vascular Endothelial Growth Factor A - metabolism | Peptide Library | Tissue Distribution | Vascular Endothelial Growth Factor A - chemistry | Endocytosis | Peptides - metabolism | Prostatic Neoplasms - genetics | Transfection | Lung - metabolism | Binding Sites | Binding, Competitive | Amino Acid Sequence | Prostatic Neoplasms - pathology | Peptide Fragments - metabolism | Peptides - chemistry | Microscopy, Confocal | Peptide Fragments - chemistry | Animals | Chromatography, Affinity | Mice, Nude | Cell Line, Tumor | Protein Binding | Mice | Mice, Inbred BALB C | Arginine - metabolism | Measurement | Synthesis | Peptides | Permeability | Properties | Vascular endothelial growth factor | Methods | Cells | Tissue | Proteases | Gene expression | Prostate cancer | Binding sites | Index Medicus | Biological Sciences
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 10/2011, Volume 108, Issue 41, pp. 16883 - 16888
Cell-penetrating peptides (CPPs), such as the HIV TAT peptide, are able to translocate across cellular membranes efficiently. A number of mechanisms, from... 
Endocytosis | Receptors | Actins | Amino acids | Lipids | Cell membranes | Hydrophobicity | Curvature | Freight | P branes | Protein transduction domain | Polyarginine | Pore-forming peptide | Antimicrobial peptide | Peptide-lipid interactions | protein transduction domain | peptide-lipid interactions | MULTIDISCIPLINARY SCIENCES | pore-forming peptide | CELL-PENETRATING PEPTIDES | ANTIMICROBIAL PEPTIDES | MOLECULAR TRANSPORTERS | LOW-TEMPERATURE | LIPOSOME-DNA COMPLEXES | PROTEIN TRANSDUCTION DOMAINS | INTRACELLULAR DELIVERY | HEPARAN-SULFATE PROTEOGLYCANS | antimicrobial peptide | ARGININE-RICH PEPTIDES | polyarginine | FUSION PROTEINS | Amino Acid Sequence | Cell-Penetrating Peptides - genetics | tat Gene Products, Human Immunodeficiency Virus - genetics | Humans | Models, Molecular | Pinocytosis | tat Gene Products, Human Immunodeficiency Virus - chemistry | Unilamellar Liposomes - metabolism | Biological Transport, Active | Models, Biological | Cytoskeleton - metabolism | Hydrophobic and Hydrophilic Interactions | Cell Membrane - metabolism | HeLa Cells | In Vitro Techniques | Cell-Penetrating Peptides - chemistry | Cell-Penetrating Peptides - metabolism | tat Gene Products, Human Immunodeficiency Virus - metabolism | Physiological aspects | Cell receptors | Research | Viral proteins | HIV (Viruses) | Cytoskeleton | Membranes | Peptides | Human immunodeficiency virus--HIV | Cells | Index Medicus | Physical Sciences
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 1/2016, Volume 113, Issue 3, pp. E291 - E299
Protein transduction domains (PTDs) are powerful nongenetic tools that allow intracellular delivery of conjugated cargoes to modify cell behavior. Their use in... 
Human embryonic stem cells | Transduction | Cell-penetrating peptides | Differentiation | Heparin-binding domain | differentiation | transduction | MULTIDISCIPLINARY SCIENCES | MECHANISMS | HEPARIN | MAMMALIAN-CELLS | IPS CELLS | PLURIPOTENT STEM-CELLS | cell-penetrating peptides | heparin-binding domain | MACROPINOCYTOSIS | GROWTH-FACTOR | PROTEINS | human embryonic stem cells | NIH 3T3 Cells | Homeodomain Proteins - metabolism | Human Embryonic Stem Cells - cytology | Humans | Mouse Embryonic Stem Cells - cytology | Mouse Embryonic Stem Cells - drug effects | Mouse Embryonic Stem Cells - metabolism | Drug Delivery Systems | Nanoparticles | Human Embryonic Stem Cells - drug effects | Integrases - metabolism | Cell Membrane - metabolism | Cell Membrane - drug effects | Cell-Penetrating Peptides - chemistry | Induced Pluripotent Stem Cells - metabolism | Protein Structure, Tertiary | Detergents - pharmacology | Human Embryonic Stem Cells - metabolism | Nanog Homeobox Protein | Induced Pluripotent Stem Cells - drug effects | Glycosaminoglycans - metabolism | Endocytosis - drug effects | Solubility | MyoD Protein - metabolism | Nucleic Acids - metabolism | Trypsin - metabolism | Amino Acid Motifs | Animals | Muscle Development - drug effects | Cell Differentiation - drug effects | Cell Proliferation - drug effects | Mice | Genome | Cell-Penetrating Peptides - metabolism | Physiological aspects | Physiological research | Cellular signal transduction | Glycosaminoglycans | Research | Proteins | Peptides | Cytoplasm | Binding sites | Stem cells | Index Medicus | Biological Sciences | PNAS Plus
Journal Article
Journal Article
Scientific Reports, ISSN 2045-2322, 09/2016, Volume 6, Issue 1, pp. 32301 - 32301
Bioactive macromolecular peptides and oligonucleotides have significant therapeutic potential. However, due to their size, they have no ability to enter the... 
HUMAN IMMUNODEFICIENCY VIRUS | GREEN FLUORESCENT PROTEIN | IN-VITRO | SPLIT GFP | VIVO | MULTIDISCIPLINARY SCIENCES | MACROPINOCYTOSIS | GFP-COMPLEMENTATION ASSAY | CELL-PENETRATING PEPTIDES | ARGININE-RICH PEPTIDES | LIVING CELLS | Cell Line | Cell-Penetrating Peptides - genetics | Green Fluorescent Proteins - metabolism | RNA, Small Interfering - genetics | Humans | Macromolecular Substances - administration & dosage | Peptides - genetics | Green Fluorescent Proteins - genetics | Binding Sites - genetics | Endosomes - metabolism | Peptides - administration & dosage | Endocytosis | Peptides - metabolism | MCF-7 Cells | Biological Products - metabolism | Cell Line, Tumor | Time-Lapse Imaging - methods | Biological Products - administration & dosage | RNA, Small Interfering - administration & dosage | Drug Delivery Systems - methods | Macromolecular Substances - metabolism | Microscopy, Fluorescence | Cell-Penetrating Peptides - metabolism | RNA, Small Interfering - metabolism | Peptides | Indole | Macromolecules | Oligonucleotides | Cytotoxicity | Amino acids | siRNA | Hydrophobicity | Tat protein | Polyethylene glycol | Intracellular | Cytoplasm | Endosomes | Index Medicus | Medical Biotechnology | Medical and Health Sciences | Medicin och hälsovetenskap | Medical Biotechnology (with a focus on Cell Biology (including Stem Cell Biology), Molecular Biology, Microbiology, Biochemistry or Biopharmacy) | Medicinsk bioteknologi (med inriktning mot cellbiologi (inklusive stamcellsbiologi), molekylärbiologi, mikrobiologi, biokemi eller biofarmaci) | Medicinsk bioteknologi
Journal Article
ACS Nano, ISSN 1936-0851, 2013, Volume 7, Issue 5, pp. 3797 - 3807
Journal Article
Science, ISSN 0036-8075, 9/2004, Volume 305, Issue 5689, pp. 1466 - 1470
BCL-2 family proteins constitute a critical control point for the regulation of apoptosis. Protein interaction between BCL-2 members is a prominent mechanism... 
T lymphocytes | Leukemia | Cell lines | Hydrocarbons | Fluorescence | Amino acids | Cytochromes | Reports | Apoptosis | Vehicles | Endosomes | CYTOCHROME-C | DOMAIN | MULTIDISCIPLINARY SCIENCES | MACROPINOCYTOSIS | NMR STRUCTURE | CELL-PENETRATING PEPTIDES | CHROMOSOMAL BREAKPOINT | FOLLICULAR LYMPHOMA | DEATH | BAK | PROTEIN TRANSDUCTION | Neoplasm Transplantation | Alkenes | Mitochondria, Liver - metabolism | Humans | BH3 Interacting Domain Death Agonist Protein | Transplantation, Heterologous | Bridged-Ring Compounds - metabolism | Proto-Oncogene Proteins - chemistry | Endosomes - metabolism | Dose-Response Relationship, Drug | Proto-Oncogene Proteins c-bcl-2 - metabolism | Molecular Mimicry | Bridged-Ring Compounds - chemistry | Peptides - chemical synthesis | Peptides - metabolism | Bridged-Ring Compounds - pharmacology | Protein Engineering | Carrier Proteins - chemistry | Cell Membrane - metabolism | Leukemia, Experimental - pathology | Protein Structure, Tertiary | Peptides - chemistry | Protein Structure, Secondary | Jurkat Cells | Leukemia, Experimental - drug therapy | Cytochromes c - metabolism | Leukemic Infiltration | Mice, SCID | Cell Division - drug effects | Peptides - pharmacology | Mitochondria, Liver - drug effects | Peptide Fragments - chemistry | Animals | Cell Line, Tumor | Protein Binding | Mice | Bridged-Ring Compounds - chemical synthesis | Physiological aspects | Research | Proteins | Peptides | Cells | Index Medicus
Journal Article
Nucleic Acids Research, ISSN 0305-1048, 05/2011, Volume 39, Issue 9, pp. 3972 - 3987
Journal Article
Journal of the American Chemical Society, ISSN 0002-7863, 11/2017, Volume 139, Issue 44, pp. 15628 - 15631
Here we describe the utility of peptide macrocyclization through perfluoroaryl-cysteine SNAr chemistry to improve the ability of peptides to cross the... 
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