Site-directed photoproteolysis of 8-oxoguanine DNA glycosylase 1 (OGG1) by specific porphyrin-protein probe conjugates: a strategy to improve the effectiveness of photodynamic therapy for cancer.
Site-directed photoproteolysis of 8-oxoguanine DNA glycosylase 1 (OGG1) by specific porphyrin-protein probe conjugates: a strategy to improve the effectiveness of photodynamic therapy for cancer.
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通过特定的卟啉-蛋白质探针结合物对 8-氧代鸟嘌呤 DNA 糖基化酶 1 (OGG1) 进行定点光蛋白水解:提高癌症光动力疗法有效性的策略。
DOI:
10.1016/j.jphotobiol.2006.12.004
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发表时间:
2007
期刊:
影响因子:
--
通讯作者:
Berrios,Miguel
中科院分区:
文献类型:
--
作者:
Conlon,KimberlyA;Berrios,Miguel
The specific light-induced, non-enzymatic photolysis of mOGG1 by porphyrin-conjugated or rose bengal-conjugated streptavidin and porphyrin-conjugated or rose bengal-conjugated first specific or secondary anti-IgG antibodies is reported. The porphyrin chlorin e6 and rose bengal were conjugated to either streptavidin, rabbit anti-mOGG1 primary specific antibody fractions or goat anti-rabbit IgG secondary antibody fractions. Under our experimental conditions, visible light of wavelengths greater than 600nm induced the non-enzymatic degradation of mOGG1 when this DNA repair enzyme either directly formed a complex with chlorin e6-conjugated anti-mOGG1 primary specific antibodies or indirectly formed complexes with either streptavidin-chlorin e6 conjugates and biotinylated first specific anti-mOGG1 antibodies or first specific anti-mOGG1 antibodies and chlorin e6-conjugated anti-rabbit IgG secondary antibodies. Similar results were obtained when rose bengal was used as photosensitizer instead of chlorin e6. The rate of the photochemical reaction of mOGG1 site-directed by all three chlorin e6 antibody complexes was not affected by the presence of the singlet oxygen scavenger sodium azide. Site-directed photoactivatable probes having the capacity to generate reactive oxygen species (ROS) while destroying the DNA repair system in malignant cells and tumors may represent a powerful strategy to boost selectivity, penetration and efficacy of current photodynamic (PDT) therapy methodologies.
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DOI:
10.1016/s1011-1344(01)00241-x
发表时间:
2001-12
期刊:
Journal of photochemistry and photobiology. B, Biology
影响因子:
--
作者:
K. Conlon;M. Berrios
通讯作者:
K. Conlon;M. Berrios
DOI:
10.1016/s0021-9258(19)36531-7
发表时间:
1993-09
期刊:
The Journal of biological chemistry
影响因子:
--
作者:
T. Bessho;K. Tano;H. Kasai;E. Ohtsuka;S. Nishimura
通讯作者:
T. Bessho;K. Tano;H. Kasai;E. Ohtsuka;S. Nishimura
影响因子:
1.1
作者:
Kimberly A. Conion;A. Grollman;M. Berrios
通讯作者:
M. Berrios
DOI:
10.20772/cancersci1959.75.12_1037
发表时间:
1984
期刊:
Gan
影响因子:
--
作者:
H. Kasai;H. Tanooka;S. Nishimura
通讯作者:
S. Nishimura
影响因子:
10.3
作者:
del Carmen, MG;Rizvi, I;Hasan, T
通讯作者:
Hasan, T