Polypeptides with quaternary phosphonium side chains: Synthesis, characterization, and cell-penetrating properties

Biomacromolecules

Volumn 15, Issue 4, 2014, Pages 1491-1497

  Song, Ziyuan ^a   Zheng, Nan ^a   Ba, Xiaochu ^b   Yin, Lichen ^a   Zhang, Rujing ^a   Ma, Liang ^a   Cheng, Jianjun ^a  

^a University of Illinois at Urbana Champaign   (United States)

^b UNIVERSITY OF ILLINOIS AT URBANA CHAMPAIGN   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACIDS; CELL MEMBRANES; CHAINS; CONFORMATIONS; CYTOLOGY; IONIC STRENGTH; SUBSTITUTION REACTIONS;

CONTROLLED RING-OPENING POLYMERIZATIONS; HELICAL CONFORMATION; L-GLUTAMATE; LOW CYTOTOXICITIES; MEMBRANE TRANSDUCTION; N-CARBOXYANHYDRIDE; NUCLEOPHILIC SUBSTITUTION REACTIONS; TRIETHYLPHOSPHINE;

POLYPEPTIDES;

CELL PENETRATING PEPTIDE; CHLORINE; GLUTAMIC ACID; MONOMER; PHOSPHONIUM DERIVATIVE; POLYPEPTIDE; PEPTIDE; PHOSPHOROUS ACID; POLYGLUTAMIC ACID;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CELL MEMBRANE; CHEMICAL STRUCTURE; CIRCULAR DICHROISM; COLUMN CHROMATOGRAPHY; CONFOCAL LASER MICROSCOPY; CONTROLLED STUDY; CYTOTOXICITY; ENDOCYTOSIS; GEL PERMEATION CHROMATOGRAPHY; HUMAN; HUMAN CELL; IONIC STRENGTH; MEMBRANE PERMEABILITY; MTT ASSAY; NUCLEOPHILICITY; PH; POLYMERIZATION; PRIORITY JOURNAL; PROTEIN ANALYSIS; PROTEIN CONFORMATION; PROTEIN SECONDARY STRUCTURE; PROTON NUCLEAR MAGNETIC RESONANCE; RACEMIC MIXTURE; RING OPENING; STEREOCHEMISTRY; SUBSTITUTION REACTION; SYNTHESIS; CHEMISTRY; DRUG EFFECTS; HELA CELL LINE; STRUCTURE ACTIVITY RELATION;

CELL MEMBRANE; CHEMISTRY TECHNIQUES, SYNTHETIC; HELA CELLS; HUMANS; PEPTIDES; PHOSPHOROUS ACIDS; POLYGLUTAMIC ACID; PROTEIN CONFORMATION; STRUCTURE-ACTIVITY RELATIONSHIP;

EID: 84898662280     PISSN: 15257797     EISSN: 15264602     Source Type: Journal    
DOI: 10.1021/bm5001026     Document Type: Article

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