Three routes to modulate the pore size of the Mscl channel/nanovalve

ACS Nano

Volumn 6, Issue 2, 2012, Pages 1134-1141

  Yang, Li Min ^a   Wray, Robin ^a   Parker, Juandell ^a   Wilson, Danyell ^b,d   Duran, Randolph S ^c   Blount, Paul ^a  

^a UNIVERSITY OF TEXAS SOUTHWESTERN MEDICAL CENTER   (United States)

^b University of Florida ^*  (United States)

^c LOUISIANA STATE UNIVERSITY   (United States)

^d H LEE MOFFITT CANCER CENTER AND RESEARCH INSTITUTE   (United States)

Author keywords

biosensor; conductance; drug release device; nanopore; osmoregulation

Indexed keywords

BIOSENSORS; CONTROLLED DRUG DELIVERY; ELECTRIC CONDUCTANCE; HEAVY METALS; MICROELECTRONICS; NANOPORES; OSMOSIS; PORE SIZE; TARGETED DRUG DELIVERY;

CARBOXYL-TERMINAL; DRUG RELEASE; GENETICALLY MODIFIED; MECHANOSENSITIVE CHANNEL; METAL COORDINATION; OSMOREGULATION; TRANSMEMBRANES; VARIOUS FUNCTIONS;

X RAY CRYSTALLOGRAPHY;

ESCHERICHIA COLI PROTEIN; HEAVY METAL; ION CHANNEL; MSCL PROTEIN, E COLI;

AMINO ACID SEQUENCE; ARTICLE; BINDING SITE; CELL MEMBRANE; CHANNEL GATING; CHEMICAL STRUCTURE; CHEMISTRY; CYTOLOGY; CYTOPLASM; ESCHERICHIA COLI; GENETICS; INSTRUMENTATION; METABOLISM; METHODOLOGY; NANOTECHNOLOGY; POROSITY; PROTEIN ENGINEERING; PROTEIN SECONDARY STRUCTURE;

AMINO ACID SEQUENCE; BINDING SITES; CELL MEMBRANE; CYTOPLASM; ESCHERICHIA COLI; ESCHERICHIA COLI PROTEINS; ION CHANNEL GATING; ION CHANNELS; METALS, HEAVY; MODELS, MOLECULAR; NANOTECHNOLOGY; POROSITY; PROTEIN ENGINEERING; PROTEIN STRUCTURE, SECONDARY;

EID: 84857769134     PISSN: 19360851     EISSN: 1936086X     Source Type: Journal    
DOI: 10.1021/nn203703j     Document Type: Article

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