A pH responsive fluorescent probe based on dye modified i-motif nucleic acids

2018 ◽  
Vol 16 (48) ◽  
pp. 9402-9408 ◽  
Author(s):  
Pan Li ◽  
Zhe Chen ◽  
Yishun Huang ◽  
Jing Li ◽  
Fan Xiao ◽  
...  

DNA-AIEgen hybrids show pH-responsive AIE effects induced by the conformational changes of DNA upon pH variation.

2020 ◽  
Vol 48 (9) ◽  
pp. e49-e49 ◽  
Author(s):  
Shreya Ghosh ◽  
Matthew J Lawless ◽  
Hanna J Brubaker ◽  
Kevin Singewald ◽  
Michael R Kurpiewski ◽  
...  

Abstract Electron paramagnetic resonance (EPR) has become an important tool to probe conformational changes in nucleic acids. An array of EPR labels for nucleic acids are available, but they often come at the cost of long tethers, are dependent on the presence of a particular nucleotide or can be placed only at the termini. Site directed incorporation of Cu2+-chelated to a ligand, 2,2′dipicolylamine (DPA) is potentially an attractive strategy for site-specific, nucleotide independent Cu2+-labelling in DNA. To fully understand the potential of this label, we undertook a systematic and detailed analysis of the Cu2+-DPA motif using EPR and molecular dynamics (MD) simulations. We used continuous wave EPR experiments to characterize Cu2+ binding to DPA as well as optimize Cu2+ loading conditions. We performed double electron-electron resonance (DEER) experiments at two frequencies to elucidate orientational selectivity effects. Furthermore, comparison of DEER and MD simulated distance distributions reveal a remarkable agreement in the most probable distances. The results illustrate the efficacy of the Cu2+-DPA in reporting on DNA backbone conformations for sufficiently long base pair separations. This labelling strategy can serve as an important tool for probing conformational changes in DNA upon interaction with other macromolecules.


1993 ◽  
Vol 291 (1) ◽  
pp. 103-107 ◽  
Author(s):  
H M Zhou ◽  
X H Zhang ◽  
Y Yin ◽  
C L Tsou

It has been previously reported that, during denaturation of creatine kinase by guanidinium chloride (GdmCl) or urea [Tsou (1986), Trends Biochem. Sci. 11, 427-429], inactivation occurs before noticeable conformational change can be detected, and it is suggested that the conformation at the active site is more easily perturbed and hence more flexible than the molecule as a whole. In this study, the thiol and amino groups at or near the active site of creatine kinase are labelled with o-phthalaldehyde to form a fluorescent probe. Both the emission intensity and anisotropy decrease during denaturation indicating exposure of this probe and increased mobility of the active site. The above conformational changes take place together with enzyme inactivation at lower GdmCl concentrations than required to bring about intrinsic fluorescence changes of the enzyme. At the same GdmCl concentration, the rate of exposure of the probe is comparable with that of inactivation and is several orders of magnitude faster than that for the unfolding of the molecule as a whole.


2001 ◽  
Vol 260 (2) ◽  
pp. 293-307 ◽  
Author(s):  
Jan Barciszewski ◽  
Janusz Jurczak ◽  
Sylwester Porowski ◽  
Thomas Specht ◽  
Volker A. Erdmann

2009 ◽  
Vol 131 (8) ◽  
pp. 2798-2799 ◽  
Author(s):  
Yi Liu ◽  
Vyacheslav S. Bryantsev ◽  
Mamadou S. Diallo ◽  
William A. Goddard III

2000 ◽  
Vol 33 (25) ◽  
pp. 9169-9172 ◽  
Author(s):  
Wei Chen ◽  
Donald A. Tomalia ◽  
James L. Thomas

2000 ◽  
Vol 33 (15) ◽  
pp. 3183-3194 ◽  
Author(s):  
Wen-You Li ◽  
Jin-Gou Xu ◽  
Xi-Wen He

Biochimie ◽  
1976 ◽  
Vol 58 (4) ◽  
pp. 395-402 ◽  
Author(s):  
Maurice Durand ◽  
Hanna N. Borazan ◽  
Jean-Claude Maurizot ◽  
Jean-Luc Dimicoli ◽  
Claude Hélène

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