Morphological characterization of self-assembled peptide nucleic acid amphiphiles

被引:24
|
作者
Lau, C
Bitton, R
Bianco-Peled, H
Schultz, DG
Cookson, DJ
Grosser, ST
Schneider, JW [1 ]
机构
[1] Carnegie Mellon Univ, Dept Chem Engn, Pittsburgh, PA 15213 USA
[2] Technion Israel Inst Technol, Dept Chem Engn, IL-32000 Haifa, Israel
[3] Technion Israel Inst Technol, InterDept Program Biotechnol, IL-32000 Haifa, Israel
[4] Univ Illinois, Dept Phys, Chicago, IL 60607 USA
[5] Australian Synchrotron Res Program, Argonne, IL 60439 USA
来源
JOURNAL OF PHYSICAL CHEMISTRY B | 2006年 / 110卷 / 18期
关键词
D O I
10.1021/jp057049h
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Peptide nucleic acid amphiphiles (PNAA) are a promising set of materials for sequence-specific separation of nucleic acids from complex mixtures. To implement PNAA in micellar separations, the morphology and size of PNAA micelles in the presence and absence of a sodium dodecyl sulfate (SDS) cosurfactant have been studied by small-angle X-ray scattering and dynamic light scattering. We find that a 6-mer PNAA with a 12-carbon n-alkane tail forms ellipsoidal micelles (a = 5.15 nm; b = 3.20 nm) above its critical micelle concentration (CMC) of 110.9 mu M. On addition of a stoichiometric amount of complementary DNA, PNAA hybridizes to DNA, suppressing the formation of PNAA micelles. At a ratio of 19:1 SDS/PNAA (total concentration = 20 mM), spherical micelles are formed with outer radius R-s = 2.67 nm, slightly larger than spherical micelles of pure SDS. Capillary electrophoresis studies show that PNAA/DNA duplexes do not comicellize with SDS micelles. No such effects are observed using noncomplementary DNA. The shape and size of the PNAA micelles is also verified by dynamic light scattering (DLS) studies. These results provide an interesting case study with competing electrostatic, hydrophobic, and hydrogen-bonding interactions in micellar systems and make possible the use of PNAA in micellar separations of DNA oligomers.
引用
收藏
页码:9027 / 9033
页数:7
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