Circular dichroism as a measure of superhelix density : A theoretical study

In chromatin, the DNA helix is itself helically coiled to form a superhelix, the tightness of which affects the transcription accessibility. Elucidation of the possible role of supercoiling in the control of gene expression requires an accurate and non-destructive method to measure superhelix density, and in this paper we show how the sensitivity of circular dichroism (c.d.) to supercoiling can be exploited. The chromatin c.d. at 270 nm shows a reduction to 45-70% of that of straight, non-supercoiled B-DNA. This has been attributed variously to secondary structural changes or tertiary interactions between adjacent superhelical turns. We investigate this effect by calculating the ratio of the c.d. of supercoiled and of straight DNA as a function of superhelix density with the use of the Tinoco model, but introducing a novel metric technique to relate c.d. to curvature. Tertiary interactions are shown to cancel one another, leaving the c.d. of chromatin unchanged, so the observed depression must arise from secondary structural effects. We investigate c.d. as a function of secondary structure, and find that base-twisting affects the c.d. much more than base-tilting, and can produce a strong depression. We therefore introduce a model of supercoiled DNA with base-twisting in proportion to the local Riemann curvature of the bent helix, and this reduces the chromatin c.d. to 70% of that of non-supercoiled DNA. Further reduction to 45 % is achieved if chromatin forms a left-hand supersuperhelix. These results suggest that c.d. has considerable potential as a quantitative measure of supercoiling.

2021 ◽  
Vol 22 (6) ◽  
pp. 2937
Author(s):  
Monika Halat ◽  
Magdalena Klimek-Chodacka ◽  
Jagoda Orleanska ◽  
Malgorzata Baranska ◽  
Rafal Baranski

The Streptococcus pyogenes Cas9 protein (SpCas9), a component of CRISPR-based immune system in microbes, has become commonly utilized for genome editing. This nuclease forms a ribonucleoprotein (RNP) complex with guide RNA (gRNA) which induces Cas9 structural changes and triggers its cleavage activity. Here, electronic circular dichroism (ECD) spectroscopy was used to confirm the RNP formation and to determine its individual components. The ECD spectra had characteristic features differentiating Cas9 and gRNA, the former showed a negative/positive profile with maxima located at 221, 209 and 196 nm, while the latter revealed positive/negative/positive/negative pattern with bands observed at 266, 242, 222 and 209 nm, respectively. For the first time, the experimental ECD spectrum of the gRNA:Cas9 RNP complex is presented. It exhibits a bisignate positive/negative ECD couplet with maxima at 273 and 235 nm, and it differs significantly from individual spectrum of each RNP components. Additionally, the Cas9 protein and RNP complex retained biological activity after ECD measurements and they were able to bind and cleave DNA in vitro. Hence, we conclude that ECD spectroscopy can be considered as a quick and non-destructive method of monitoring conformational changes of the Cas9 protein as a result of Cas9 and gRNA interaction, and identification of the gRNA:Cas9 RNP complex.


RSC Advances ◽  
2013 ◽  
Vol 3 (26) ◽  
pp. 10242 ◽  
Author(s):  
Eduardo Troche-Pesqueira ◽  
Ignacio Pérez-Juste ◽  
Armando Navarro-Vázquez ◽  
María Magdalena Cid

Author(s):  
Sascha Jähnigen ◽  
Daniel Sebastiani ◽  
Rodolphe Vuilleumier

We present a computational study of vibrational circular dichroism (VCD) in solutions of (S)-lactic acid, relying on ab initio molecular dynamics (AIMD) and full solvation with bulk water. We discuss...


1985 ◽  
Vol 63 (11) ◽  
pp. 1167-1175 ◽  
Author(s):  
Charles G. Suhayda ◽  
Alfred Haug

At a molar excess of [citrate]/[aluminum], this organic acid can protect calmodulin from aluminum binding if the metal is presented to the protein in stoichiometric micromolar quantities, as judged by fluorescence and circular dichroism spectroscopy. Similar citrate concentrations are also capable of fully restoring calmodulin's hydrophobic surface exposure to that of the native protein when calmodulin was initially damaged by aluminum binding. Fluoride anions are equally effective in restoring calmodulin's native structure as determined by fluorescence spectroscopy. Measurements of the kinetics of citrate-mediated aluminum removal also indicated that the metal ions are completely removed from calmodulin, consistent with results derived from atomic absorption experiments. On the other hand, results from circular dichroism studies indicated that citrate-mediated aluminum removal from calmodulin can only partially restore the α-helix content to that originally present in apocalmodulin or in calcium–calmodulin, dependent upon the absence or presence of calcium ions. The results that chelators like citrate can protect calmodulin from aluminum injury may provide a conceptual understanding of physiological observations regarding aluminum-tolerant plant species which are generally rich in certain organic acids.


2020 ◽  
Vol 14 (5) ◽  
Author(s):  
James Lourembam ◽  
Xiaojiang Yu ◽  
Maria Patricia Rouelli Sabino ◽  
Michael Tran ◽  
Roslyn Wan Teng Ang ◽  
...  

ACS Photonics ◽  
2016 ◽  
Vol 3 (4) ◽  
pp. 578-583 ◽  
Author(s):  
Maxim L. Nesterov ◽  
Xinghui Yin ◽  
Martin Schäferling ◽  
Harald Giessen ◽  
Thomas Weiss

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