2023
DOI: 10.1016/j.biochi.2022.12.019
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Guidelines for G-quadruplexes: I. In vitro characterization

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Cited by 15 publications
(17 citation statements)
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“…To this end, we selected a panel of 36 sequences, containing four consecutive blocks of at least two guanines, distributed both on the chromosome and on the mini-chromosomes. To demonstrate the formation of the G4, we used a variety of methods ( 57 ). FRET-MC enables the testing of several sequences in a parallel fashion ( 44 ).…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation

G-quadruplexes inHaloferax volcanii

Aktary,
Cucchiarini,
Vesco
et al. 2024
Preprint
Self Cite
“…To this end, we selected a panel of 36 sequences, containing four consecutive blocks of at least two guanines, distributed both on the chromosome and on the mini-chromosomes. To demonstrate the formation of the G4, we used a variety of methods ( 57 ). FRET-MC enables the testing of several sequences in a parallel fashion ( 44 ).…”
Section: Resultsmentioning
confidence: 99%
“…As several techniques are recommended to definitively demonstrate G4 formation ( 57 ), we used an alternative approach and investigated whether the fluorescence emission of G4 probes such as thioflavin T ( 45 ) and NMM ( 58 ) was increased in the presence of potential G4-forming H. volcanii sequences. When compared to the negative and positive controls, most sequences induced an increase in fluorescence emission of both G4 light probes (Figure 2B and 2C).…”
Section: Resultsmentioning
confidence: 99%

G-quadruplexes inHaloferax volcanii

Aktary,
Cucchiarini,
Vesco
et al. 2024
Preprint
Self Cite
“…There is a growing number of bioinformatic tools for UNas prediction and biophysical characterization [45,[56][57][58][59] as well as for determining their roles in various diseases including cancer [60,61]. Contemporary, specific antibodies against cruciforms [62,63], lefthanded nucleic acids [64], G-quadruplexes [65], and i-motifs [66] have also been developed, allowing effective analyses of UNas both in vitro and in situ.…”
Section: Future Perspectivesmentioning
confidence: 99%
“…Furthermore, the polymorphism of G4s depends on the number of chains, on the size of the oligonucleotide sequence, strand polarity and loops. [12][13][14] Diverse G4s systems have been investigated for loading multiple classes of anticancer drugs, such as acridine, 15 doxorubicin, 16 phthalocyanines [17][18][19] and porphyrin derivatives. 8,20 Additionally, it has been shown that certain G4s have the ability to recognize specific cancer markers per se, due to the high affinity to specific nucleic acids or proteins expressed in cancer cells.…”
Section: Introductionmentioning
confidence: 99%
“…Furthermore, the polymorphism of G4s depends on the number of chains, on the size of the oligonucleotide sequence, strand polarity and loops. 12–14…”
Section: Introductionmentioning
confidence: 99%