AUTHOR=Nakashima Masaaki , Ode Hirotaka , Suzuki Koji , Fujino Masayuki , Maejima Masami , Kimura Yuki , Masaoka Takashi , Hattori Junko , Matsuda Masakazu , Hachiya Atsuko , Yokomaku Yoshiyuki , Suzuki Atsuo , Watanabe Nobuhisa , Sugiura Wataru , Iwatani Yasumasa TITLE=Unique Flap Conformation in an HIV-1 Protease with High-Level Darunavir Resistance JOURNAL=Frontiers in Microbiology VOLUME=7 YEAR=2016 URL=https://www.frontiersin.org/journals/microbiology/articles/10.3389/fmicb.2016.00061 DOI=10.3389/fmicb.2016.00061 ISSN=1664-302X ABSTRACT=

Darunavir (DRV) is one of the most powerful protease inhibitors (PIs) for treating human immunodeficiency virus type-1 (HIV-1) infection and presents a high genetic barrier to the generation of resistant viruses. However, DRV-resistant HIV-1 infrequently emerges from viruses exhibiting resistance to other protease inhibitors. To address this resistance, researchers have gathered genetic information on DRV resistance. In contrast, few structural insights into the mechanism underlying DRV resistance are available. To elucidate this mechanism, we determined the crystal structure of the ligand-free state of a protease with high-level DRV resistance and six DRV resistance-associated mutations (including I47V and I50V), which we generated by in vitro selection. This crystal structure showed a unique curling conformation at the flap regions that was not found in the previously reported ligand-free protease structures. Molecular dynamics simulations indicated that the curled flap conformation altered the flap dynamics. These results suggest that the preference for a unique flap conformation influences DRV binding. These results provide new structural insights into elucidating the molecular mechanism of DRV resistance and aid to develop PIs effective against DRV-resistant viruses.