In vitro reconstitution of SV40 particles that are composed of VP1/2/3 capsid proteins and nucleosomal DNA and direct efficient gene transfer

Virology

Volumn 420, Issue 1, 2011, Pages 1-9

  Enomoto, Teruya ^a   Kukimoto, Iwao ^b   Kawano, Masa Aki ^c   Yamaguchi, Yuki ^a   Berk, Arnold J ^d   Handa, Hiroshi ^a  

^a TOKYO INSTITUTE OF TECHNOLOGY   (Japan)

^b NATIONAL INSTITUTE OF INFECTIOUS DISEASES   (Japan)

^c SAITAMA MEDICAL UNIVERSITY   (Japan)

^d UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

Gene expression; Gene transfer; Hyper acetylated histone; In vitro reconstitution; Minor capsid proteins VP2 3; Nucleosomal DNA; SV40

Indexed keywords

HISTONE; PROTEIN VP1; PROTEIN VP2; PROTEIN VP3; VIRUS DNA;

ARTICLE; CELL SURFACE; CONTROLLED STUDY; GENE TARGETING; GENE TRANSFER; HUMAN; HUMAN CELL; IN VITRO STUDY; MAMMAL CELL; NONHUMAN; NUCLEOSOME; POLYOMA VIRUS; PRIORITY JOURNAL; PROTEIN EXPRESSION; PROTEIN FUNCTION; REPORTER GENE; SIMIAN VIRUS 40; VIRAL GENE DELIVERY SYSTEM; VIRION; VIRUS GENOME;

ANIMALS; CAPSID PROTEINS; CELL LINE; DNA; GENE EXPRESSION; GENE TRANSFER TECHNIQUES; GENETIC VECTORS; HUMANS; NUCLEOSOMES; SIMIAN VIRUS 40; VIRION; VIRUS ASSEMBLY;

MAMMALIA; MIRIDAE; POLYOMAVIRIDAE;

EID: 80053386878     PISSN: 00426822     EISSN: 10960341     Source Type: Journal    
DOI: 10.1016/j.virol.2011.08.014     Document Type: Article

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