Thermodynamics of DNA Condensation Induced by Poly(ethylene glycol)-block-polylysine through Polyion Complex Micelle Formation

被引:47
作者
Kim, Wankee [1 ]
Yamasaki, Yuichi [1 ,4 ]
Jang, Woo-Dong [1 ]
Kataoka, Kazunori [1 ,2 ,3 ,4 ]
机构
[1] Univ Tokyo, Dept Mat Sci & Engn, Grad Sch Engn, Bunkyo Ku, Tokyo 1138656, Japan
[2] Univ Tokyo, Ctr Dis Biol & Integrat Med, Grad Sch Med, Bunkyo Ku, Tokyo 1130033, Japan
[3] Univ Tokyo, Ctr NanoBio Integrat, Bunkyo Ku, Tokyo 1138656, Japan
[4] Japan Sci & Technol Agcy JST, Core Res Program Evolut Sci & Technol CREST, Kawaguchi, Saitama 3320012, Japan
关键词
COUNTERION RELEASE; ACID INTERACTIONS; PLASMID DNA; L-LYSINE; BINDING; COPOLYMERS; PROTEINS; FORCES; MODEL;
D O I
10.1021/bm901305p
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Isothermal titration calorimetry (ITC) was carried out to explore the condensation process of plasmid DNA (pDNA) molecules induced by poly(ethylene glycol)-poly(L-lysine) block copolymer (PEG-PLL) as a condensing agent. The ITC curves measured can be divided into two distinctive endothermic binding processes: the first was the binding of PEG-PLL to the elongated pDNA, and the second was the binding that accompanied the pDNA conformational transition. The thermodynamic parameters were obtained by fitting each ITC curve using our recently developed fitting method. The binding of PEG-PLL to the pDNA was accompanied by a small increase in enthalpy, a large increase in entropy, and a large decrease in free energy. The binding stabilized as the polymerization degree of PLL on PEG-PLL increased and the salt concentration decreased. Changes in the thermodynamic parameters are discussed in relation to both the polymerization degree of PLL on PEG-PLL and the salt concentration.
引用
收藏
页码:1180 / 1186
页数:7
相关论文
共 36 条
[1]   Preparation of cationic comb-type copolymers having high density of PEG graft chains for gene carriers [J].
Choi, Sung Won ;
Yamayoshi, Asako ;
Hirai, Miwa ;
Yamano, Takeshi ;
Takagi, Motoki ;
Sato, Ayumi ;
Kano, Arihiro ;
Shimamoto, Akira ;
Maruyama, Atsushi .
MACROMOLECULAR SYMPOSIA, 2007, 249 :312-316
[2]   Polyethylene glycol-grafted poly-L-lysine as polymeric gene carrier [J].
Choi, YH ;
Liu, F ;
Kim, JS ;
Choi, YK ;
Park, JS ;
Kim, SW .
JOURNAL OF CONTROLLED RELEASE, 1998, 54 (01) :39-48
[3]   Thermodynamic analysis of polycation-DNA interaction applying titration microcalorimetry [J].
Ehtezazi, T ;
Rungsardthong, U ;
Stolnik, S .
LANGMUIR, 2003, 19 (22) :9387-9394
[4]   ISOTHERMAL TITRATION CALORIMETRY [J].
FREIRE, E ;
MAYORGA, OL ;
STRAUME, M .
ANALYTICAL CHEMISTRY, 1990, 62 (18) :A950-A959
[5]  
*GEN THER CLIN TRI, DAT IND VECT GEN TYP
[6]   Counterion-mediated attraction between two like-charged rods [J].
Ha, BY ;
Liu, AJ .
PHYSICAL REVIEW LETTERS, 1997, 79 (07) :1289-1292
[7]   FORMATION OF POLYION COMPLEX MICELLES IN AN AQUEOUS MILIEU FROM A PAIR OF OPPOSITELY-CHARGED BLOCK-COPOLYMERS WITH POLY(ETHYLENE GLYCOL) SEGMENTS [J].
HARADA, A ;
KATAOKA, K .
MACROMOLECULES, 1995, 28 (15) :5294-5299
[8]   Polyion complex micelles as vectors in gene therapy - pharmacokinetics and in vivo gene transfer [J].
Harada-Shiba, M ;
Yamauchi, K ;
Harada, A ;
Takamisawa, I ;
Shimokado, K ;
Kataoka, K .
GENE THERAPY, 2002, 9 (06) :407-414
[9]  
Hashimoto T, 2005, NON-VIRAL GENE THERAPY: GENE DESIGN AND DELIVERY, P35, DOI 10.1007/4-431-27879-6_4
[10]   Design and biophysical characterization of novel polycationic ε-peptides for DNA compaction and delivery [J].
Huang, Dandan ;
Korolev, Nikolay ;
Eom, Khee Dong ;
Tam, James P. ;
Nordenskiold, Lars .
BIOMACROMOLECULES, 2008, 9 (01) :321-330