Mechanistic differences in DNA nanoparticle formation in the presence of oligolysines and poly-L-lysine

被引:43
作者
Nayvelt, Irina
Thomas, Thresia
Thomas, T. J.
机构
[1] Univ Med & Dent New Jersey, Robert Wood Johnson Med Sch, Dept Med, New Brunswick, NJ 08903 USA
[2] Univ Med & Dent New Jersey, Robert Wood Johnson Med Sch, Dept Environm & Occupat Med, New Brunswick, NJ 08903 USA
[3] Canc Inst New Jersey, New Brunswick, NJ 08903 USA
[4] Environm & Occupat Hlth Sci Inst, Piscataway, NJ 08854 USA
[5] Rutgers State Univ, Grad Program Nutr Sci, New Brunswick, NJ 08903 USA
关键词
D O I
10.1021/bm0605863
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
We studied the effectiveness of trilysine (Lys(3)), tetralysine (Lys(4)), pentalysine (Lys(5)), and poly-L-lysine (PLL) (MW 50000) on lambda-DNA nanoparticle formation and characterized the size, shape, and stability of nanoparticles. Light scattering experiments showed EC50 (lysine concentration at 50% DNA compaction) values of similar to 0.0036, 2, and 20 mu mol/L, respectively, for PLL, Lys(5), and Lys(4) at 10 mM [Na+]. Plots of log EC50 versus log [Na+] showed positive slopes of 1.09 and 1.7, respectively, for Lys(4) and Lys(5) and a negative slope of -0.1 for PLL. Hydrodynamic radii of oligolysine condensed particles increased (48-173 nm) with increasing [Na+], whereas no significant change occurred to nanoparticles formed with PLL. There was an increase in the size of nanoparticles formed with Lys(5) at > 40 degrees C, whereas no such change occurred with PLL. The DNA melting temperature increased with oligolysine concentration. These results indicate distinct differences in the mechanism(s) by which oligolysines and PLL provoke DNA condensation to nanoparticles.
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页码:477 / 484
页数:8
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