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Peptides derived from the C-terminal heptad repeat region (CHR) of HIV-1 gp41 are potentfusion inhibitors by targeting the N-terminal heptad repeat region (NHR).We have recentlyidentified that the unique M-T hook structure preceding the pocketbinding motifof CHR peptides can greatly enhance the binding of inhibitors to the NHR pocket thus improvingthe anti-HIV activity.