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自组装肽核酸两亲分子的形态学表征

Morphological characterization of self-assembled peptide nucleic acid amphiphiles.

作者信息

Lau Cheryl, Bitton Ronit, Bianco-Peled Havazelet, Schultz David G, Cookson David J, Grosser Shane T, Schneider James W

机构信息

Department of Chemical Engineering, Carnegie Mellon University, Pittsburgh, Pennsylvania 15213-3890, USA.

出版信息

J Phys Chem B. 2006 May 11;110(18):9027-33. doi: 10.1021/jp057049h.

Abstract

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 microM. 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 Rs = 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.

摘要

肽核酸两亲分子(PNAA)是一类很有前景的材料,可用于从复杂混合物中对核酸进行序列特异性分离。为了在胶束分离中应用PNAA,通过小角X射线散射和动态光散射研究了在存在和不存在十二烷基硫酸钠(SDS)助表面活性剂的情况下PNAA胶束的形态和大小。我们发现,具有12碳正构烷烃尾的6聚体PNAA在其110.9微摩尔的临界胶束浓度(CMC)以上形成椭圆形胶束(a = 5.15纳米;b = 3.20纳米)。加入化学计量的互补DNA后,PNAA与DNA杂交,抑制了PNAA胶束的形成。在SDS/PNAA比例为19:1(总浓度 = 20毫摩尔)时,形成了外半径Rs = 2.67纳米的球形胶束,略大于纯SDS的球形胶束。毛细管电泳研究表明,PNAA/DNA双链体不会与SDS胶束共胶束化。使用非互补DNA未观察到此类效应。动态光散射(DLS)研究也验证了PNAA胶束的形状和大小。这些结果提供了一个有趣的案例研究,涉及胶束系统中相互竞争的静电作用、疏水作用和氢键作用,并使得PNAA可用于DNA寡聚物的胶束分离成为可能。

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