Réfrégiers M, Laigle A, Jollès B, Chinsky L
Laboratoire de Physicochimie Biomoléculaire et Cellulaire, URA CNRS 2056, Université, P. et M. Curie, Paris, France.
J Biomol Struct Dyn. 1996 Dec;14(3):365-71. doi: 10.1080/07391102.1996.10508131.
In vitro degradation of antisense oligonucleotides protected or not on their 3' side against enzymatic attack by a naturally forming hairpin has been studied by fluorescence resonance energy transfer (FRET). The two oligonucleotides d(5"TTCTCGCGAAGC3') forming the hairpin and d(5"TTCTCCGGAAGC3') as a control were labeled on their 5' side by tetramethylrhodamine and on their 3' side by fluorescein. Fluorescein has been shown not to hinder the hairpin formation and to give an additional protection against nucleases. The FRET technique proved adequate for an in situ study of these protected antisense oligonucleotides in living cells.
通过荧光共振能量转移(FRET)研究了3'端有或没有受到自然形成的发夹结构保护以抵抗酶攻击的反义寡核苷酸的体外降解情况。形成发夹结构的两条寡核苷酸d(5"TTCTCGCGAAGC3')和作为对照的d(5"TTCTCCGGAAGC3')在其5'端用四甲基罗丹明标记,在其3'端用荧光素标记。已证明荧光素不会阻碍发夹结构的形成,并且能提供额外的抗核酸酶保护。FRET技术被证明适用于对活细胞中这些受保护的反义寡核苷酸进行原位研究。