Cationic porphyrins promote the formation of i-motif DNA and bind peripherally by a nonintercalative mechanism

被引:94
作者
Fedoroff, OY
Rangan, A
Chemeris, VV
Hurley, LH [1 ]
机构
[1] Univ Arizona, Arizona Canc Ctr, Tucson, AZ 85724 USA
[2] Univ Texas, Coll Pharm, Drug Dynam Inst, Austin, TX 78712 USA
[3] Univ Texas, Coll Pharm, Div Med Chem, Austin, TX 78712 USA
[4] Univ Arizona, Coll Pharm, Tucson, AZ 85721 USA
关键词
D O I
10.1021/bi001528j
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Telomeric C-rich strands can form a noncanonical intercalated DNA structure known as an i-motif. We have studied the interactions of the cationic porphyrin 5,10,15,20-tetra-(N-methyl-4-pyridyl)porphine (TMPyP4) with the i-motif forms of several oligonucleotides containing telomeric sequences. TMPyP4 was found to promote the formation of the i-motif DNA structure. On the basis of H-1 NMR studies, we have created a model of the i-motif-TMPyP4 complex that is consistent with all the available experimental data. Two-dimensional NOESY data prompted us to conclude that TMPyP4 binds specifically to the edge of the intercalated DNA core by a nonintercalative mechanism. Since we have shown that TMPyP4 binds to and stabilizes the G-quadruplex form of the complementary G-rich telomeric strand, this study raises the intriguing possibility that TMPyP4 can trigger the formation of unusual DNA structures in both strands of the telomeres, which may in turn explain the recently documented biological effects of TMPyP4 in cancer cells.
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收藏
页码:15083 / 15090
页数:8
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