Influence of alternating L-/D-amino acid chiralities and disulfide bond geometry on the capacity of cysteine-containing reversibe cyclic peptides to disperse carbon nanotubes

Biopolymers

Volumn 92, Issue 3, 2009, Pages 212-221

  Becraft, Eric J ^a   Klimenko, Anton S ^a   Dieckmann, Gregg R ^a  

^a UNIVERSITY OF TEXAS AT DALLAS   (United States)

Author keywords

Carbon nanotubes; Disulfide bond; Protein design; Raman spectroscopy; Reversible cyclic peptides

Indexed keywords

CYCLIC PEPTIDES; CYS RESIDUES; D-AMINO ACID; DISPERSABILITY; DISULFIDE BOND; DISULFIDE BONDS; EFFECTIVE DISPERSION; HYDROPHOBIC NATURE; L-AMINO ACIDS; POTENTIAL APPLICATIONS; PROTEIN DESIGN; REVERSIBLE CYCLIC PEPTIDES; SWNT DISPERSIONS; TERMINAL CYSTEINE;

AMINATION; AMINO ACIDS; CARBON DISULFIDE; CARBON NANOTUBES; CHIRALITY; DIALYSIS; DISPERSIONS; ENANTIOMERS; ORGANIC ACIDS; PEPTIDES; RAMAN SCATTERING; RAMAN SPECTROSCOPY; SINGLE-WALLED CARBON NANOTUBES (SWCN); STEREOCHEMISTRY;

AMINES;

AMINO ACID; CYCLOPEPTIDE; CYSTEINE; SINGLE WALLED NANOTUBE; CARBON NANOTUBE; PEPTIDE;

AMINO ACID SEQUENCE; AMINO TERMINAL SEQUENCE; ARTICLE; CARBOXY TERMINAL SEQUENCE; CHIRALITY; CONTROLLED STUDY; DIALYSIS; DISPERSION; DISULFIDE BOND; HYDROPHOBICITY; NEAR INFRARED REFLECTANCE SPECTROSCOPY; OXIDATION; PROTEIN ENGINEERING; RAMAN SPECTROMETRY; ULTRAVIOLET SPECTROSCOPY; CHEMICAL STRUCTURE; CHEMISTRY; MOLECULAR GENETICS; STEREOISOMERISM;

AMINO ACID SEQUENCE; AMINO ACIDS; CYSTEINE; MODELS, MOLECULAR; MOLECULAR SEQUENCE DATA; NANOTUBES, CARBON; PEPTIDES; PEPTIDES, CYCLIC; STEREOISOMERISM;

EID: 67549149081     PISSN: 00063525     EISSN: 10970282     Source Type: Journal    
DOI: 10.1002/bip.21186     Document Type: Article

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