Targeting of HIV gp120 by oligonucleotide‐photosensitizer conjugates

FEBS Letters

Vever-Bizet, Christine²  Boutorine, Alexandre S.¹  Brault, Daniel²  Hélène, Claude¹  Delgado, Olavio² 

[1] Laboratoire de Biophysique, Muséum National d'Histoire Naturelle, INSERM U 201, CNRS UMR 8646, 43 rue Cuvier, 75231 Paris Cedex 05, France;Laboratoire de Photobiologie, Muséum National d'Histoire Naturelle, INSERM U 201, CNRS UMR 8646, 43 rue Cuvier, 75231 Paris Cedex 05, France

关键词: HIV;    gp120;    Oligonucleotide;    Photosensitizer;    Chlorin;    Self-association;   

DOI  :  10.1016/S0014-5793(99)01583-5

学科分类：生物化学/生物物理

来源: John Wiley & Sons Ltd.

【 摘 要 】

Some guanine-rich oligonucleotides inhibit HIV infectivity through interaction with the gp120 glycoprotein. Besides, photoinactivation of viruses attracts attention for blood decontamination. The feasibility of targeting a red light-absorbing chlorin-type photosensitizer to gp120 through covalent coupling with 8-mer phosphodiester oligodeoxynucleotides is investigated. Some conjugates inhibit binding of antibodies directed to gp120. Inhibition is significantly increased upon red light activation. The activity of the conjugates correlates with their ability to self-associate, a process strongly favored by the propensity of the hydrophobic chlorin moiety to dimerize. Thus, the photosensitizer moiety both promotes structures with a higher affinity for gp120 and, upon light activation, can induce site-directed damages to the protein.

【 授权许可】

Unknown