Williams Ryan M, Nayeem Sara, Dolash Bridget D, Sooter Letha J
Basic Pharmaceutical Sciences, West Virginia University, Morgantown, West Virginia, United States of America.
PLoS One. 2014 Apr 4;9(4):e94117. doi: 10.1371/journal.pone.0094117. eCollection 2014.
The unique properties of single-wall carbon nanotubes (SWCNT) make them useful in many new technologies and applications. The interaction of DNA and SWCNT is of interest for many uses, including molecular sensors. This study determined polymerase chain reaction (PCR) efficiency in amplifying a 76 base pair DNA sequence in the presence of SWCNT, of heterogeneous "Mix" and (6,5)-enriched chiralities, associated with three DNA sequences. The dependence of PCR efficiency on the concentration of DNA:SWCNT preparations was measured, as well as their age and level of dispersion (less than one month or between four and ten months). Additionally, the ability to directly amplify the DNA sequence associated with the SWCNT scaffold was investigated. In PCRs with DNA:SWCNT preparations less than one month old, concentrations greater than or equal to 0.1 mg/mL inhibited the PCR reaction. In PCRs with older preparations, no inhibition was seen at 0.01 or 0.1 mg/mL, with amplification at 1 mg/mL in some samples. Additionally, our studies showed that the DNA directly associated with the SWCNT can be amplified using PCR. This work provides an inhibitory concentration of DNA-dispersed SWCNT in PCR reactions for different preparations as well as a basis for future DNA:SWCNT studies that require PCR amplification. This will be useful for future studies focused on the use of SWCNT in molecular sensing technologies.
单壁碳纳米管(SWCNT)的独特性质使其在许多新技术和应用中具有实用性。DNA与SWCNT的相互作用因其多种用途而备受关注,包括分子传感器。本研究测定了在存在SWCNT、异质“混合物”和(6,5)富集手性(与三种DNA序列相关)的情况下,聚合酶链反应(PCR)扩增76个碱基对DNA序列的效率。测量了PCR效率对DNA:SWCNT制剂浓度的依赖性,以及它们的保存时间和分散程度(小于一个月或四到十个月之间)。此外,还研究了直接扩增与SWCNT支架相关的DNA序列的能力。在使用保存时间小于一个月的DNA:SWCNT制剂进行的PCR反应中,浓度大于或等于0.1mg/mL会抑制PCR反应。在使用保存时间较长的制剂进行的PCR反应中,在0.01或0.1mg/mL时未观察到抑制作用,在一些样品中1mg/mL时出现扩增。此外,我们的研究表明,与SWCNT直接相关的DNA可以通过PCR进行扩增。这项工作提供了不同制剂在PCR反应中DNA分散的SWCNT的抑制浓度,以及未来需要PCR扩增的DNA:SWCNT研究的基础。这将有助于未来专注于SWCNT在分子传感技术中应用的研究。