1982
DOI: 10.1016/0020-711x(82)90174-4
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Spin-labelling of DNA with hydrazine mustard spin label (HMSL)

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1983
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Cited by 11 publications
(6 citation statements)
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“…419 Bifunctional cross-linking agents are also of limited specificity. 420,421 One solution is presented by the use of an aptamer. For example, the malachite green RNA aptamer (a 38-nucleotide sequence) is known to bind malachite green or closely related dyes such as tetramethylrosamine (TMR).…”
Section: Paramagnetic Probes For Dna and Rnamentioning
confidence: 99%
“…419 Bifunctional cross-linking agents are also of limited specificity. 420,421 One solution is presented by the use of an aptamer. For example, the malachite green RNA aptamer (a 38-nucleotide sequence) is known to bind malachite green or closely related dyes such as tetramethylrosamine (TMR).…”
Section: Paramagnetic Probes For Dna and Rnamentioning
confidence: 99%
“…592 Under the conditions of the DNA labeling, the nitroxyl group of 861 was lost, resulting in a DNA with no EPR signal. 592 This result was in sharp contrast to the nitrogen mustard spin-labeled compounds which were found 585 to alkylate the double-stranded DNA. Compound 861 was used also to spin label erythrocyte ghosts.…”
Section: G Nitroxyl (Aminoxyl) Analogsmentioning
confidence: 77%
“…582 In early studies 584 spin-labeled derivatives of nitrogen mustards were used to label DNA. The hydrazine mustard spin label 857 was reacted 585 with DNA, and the bioenvironment of the nitroxyl in the DNA was analyzed by EPR spectroscopy. Such EPR analysis revealed 585 that 857 is a base-specific reagent, alkylating preferentially guanine, as well as indicating the difference between the spectra of immobilized double-stranded DNA and the spectra of nonimmobilized single-stranded DNA.…”
Section: G Nitroxyl (Aminoxyl) Analogsmentioning
confidence: 99%
“…Early on, alkylating or acylating agents, such as compounds 13 45 and 14 46 (Figure 6, A), were used for spin labelling,47 but for the aforementioned reasons had very limited sequence selectivity. In an attempt to increase the selectivity, bifunctional cross‐linking agents, such as the hydrazine mustard spin label 16 ,48 the psoralene derivative 17 49 and the spin‐labelled cisplatin 18 ,50 were developed. Although these cross‐linking agents have a sequence selectivity that spans a few nucleotides, such as intra‐strand cross‐linking of the sequence GG for 18 , they still lack enough specificity to be generally applicable for SDSL.…”
Section: Post‐synthetic Spin Labellingmentioning
confidence: 99%