Department of Chemistry P. Corradini, University of Naples Federico II, via Cintia 4, Naples, Italy.
Biopolymers. 2010 Jun;93(6):533-48. doi: 10.1002/bip.21392.
Structural knowledge of telomeric DNA is critical for understanding telomere biology and for the utilization of telomeric DNA as a therapeutic target. Very little is known about the structure of long human DNA sequences that may form more than one quadruplex unit. Here, we report a combination of molecular dynamics simulations and experimental biophysical studies to explore the structural and dynamic properties of the human telomeric sequence (TTAGGG)(8)TT that folds into two contiguous quadruplexes. Five higher order quadruplex models were built combining known single human telomeric quadruplex structures as unique building blocks. The biophysical properties of this sequence in K(+) solution were experimentally investigated by means of analytical ultracentrifugation and UV spectroscopy. Additionally, the environments of loop adenines were probed by fluorescence studies using systematic single-substitutions of 2-aminopurine for the adenine bases. The comparison of the experimentally determined properties with the corresponding quantities predicted from the models allowed us to test the validity of each of the structural models. One model emerged whose properties are most consistent with the predictions, and which therefore is the most probable structure in solution. This structure features contiguous quadruplex units in an alternating hybrid-1-hybrid-2 conformation with a highly ordered interface composed of loop residues from both quadruplexes.
端粒 DNA 的结构知识对于理解端粒生物学以及将端粒 DNA 用作治疗靶点至关重要。关于可能形成多个四聚体单元的长人类 DNA 序列的结构,我们知之甚少。在这里,我们报告了分子动力学模拟和实验生物物理研究的结合,以探索折叠成两个连续四聚体的人类端粒序列 (TTAGGG)(8)TT 的结构和动态特性。通过将已知的单个人类端粒四聚体结构作为独特的构建块组合,构建了五个更高阶的四聚体模型。通过分析超速离心和 UV 光谱法,在 K(+) 溶液中对该序列的生物物理性质进行了实验研究。此外,通过使用 2-氨基嘌呤对腺嘌呤碱基进行系统的单取代,荧光研究探测了环腺嘌呤的环境。将实验确定的性质与模型预测的相应数量进行比较,使我们能够测试每个结构模型的有效性。一个模型脱颖而出,其性质与预测最一致,因此是溶液中最可能的结构。该结构具有连续的四聚体单元,采用交替的混合-1-混合-2 构象,具有由两个四聚体的环残基组成的高度有序界面。