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Psoralen MOP Alkyne

Psoralen MOP Alkyne is an excellent building block for developing site-specific nucleic acid probes via the well-known click chemistry, i.e., Copper-Catalyzed Azide–Alkyne Cycloaddition (CuAAC). It can be readily conjugated to azido-containing biomolecules (such as azido-modified antibodies, peptide azides and azido-modified oligos). Psoralens and their derivatives (such as 8-MOP and 4,5’8-TMP) are well known to have unique crosslinking features to DNA. However, psoralen monomers do not have sequence-specific crosslinking ability with a target DNA. Nakao et al found that 5-MOP more effectively crosslinks DNA compared to the well-known 8-MOP (https://doi.org/10.1002/cbic.202200789). Psoralen MOP Alkyne is an azide-reactive 5-MOP derivative. It is an excellent building block for preparing MOP-labeled oligos from an azido-modified oligo. The 5-MOP-conjugated oligonucleotides can be used for sequence-specific crosslinking with a target DNA, thus enabling the application of psoralen-conjugated molecules in gene transcription inhibition, gene knockout, and other genomic applications.

References

View all 27 references: Citation Explorer
UVA and UVB-Induced 8-Methoxypsoralen Photoadducts and a Novel Method for their Detection by Surface-Enhanced Laser Desorption Ionization Time-of-Flight Mass Spectrometry (SELDI-TOF MS).
Authors: Buhimschi, Alexandru D and Gasparro, Francis P
Journal: Photochemistry and photobiology (2014): 241-6
Sak1 kinase interacts with Pso2 nuclease in response to DNA damage induced by interstrand crosslink-inducing agents in Saccharomyces cerevisiae.
Authors: Munari, Fernanda M and Revers, Luis F and Cardone, Jacqueline M and Immich, Bruna F and Moura, Dinara J and Guecheva, Temenouga N and Bonatto, Diego and Laurino, Jomar P and Saffi, Jenifer and Brendel, Martin and Henriques, João A P
Journal: Journal of photochemistry and photobiology. B, Biology (2014): 241-53
Psoralen-induced DNA adducts are substrates for the base excision repair pathway in human cells.
Authors: Couvé-Privat, Sophie and Macé, Gaëtane and Rosselli, Filippo and Saparbaev, Murat K
Journal: Nucleic acids research (2007): 5672-82
An in vivo analysis of MMC-induced DNA damage and its repair.
Authors: Lee, Young-Ju and Park, Su-Jung and Ciccone, Samantha L M and Kim, Chong-Rak and Lee, Suk-Hee
Journal: Carcinogenesis (2006): 446-53
3-Alkyl- and 3-aryl-7H-furo[3,2-g]-1-benzopyran-7-ones: synthesis, photoreactivity, and fluorescence properties.
Authors: Körner, Paul
Journal: Archiv der Pharmazie (2002): 187-99
Page updated on November 19, 2024

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Physical properties

Molecular weight

325.32

Solvent

DMSO

Storage, safety and handling

H-phraseH303, H313, H333
Hazard symbolXN
Intended useResearch Use Only (RUO)
R-phraseR20, R21, R22

Storage

Freeze (< -15 °C); Minimize light exposure
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