Mv. Hosur et al., INFLUENCE OF STEREOCHEMISTRY ON ACTIVITY AND BINDING MODES FOR C(2) SYMMETRY-BASED DIOL INHIBITORS OF HIV-1 PROTEASE, Journal of the American Chemical Society, 116(3), 1994, pp. 847-855
The incorporation of C-2 Symmetry has become a useful paradigm in the
design of active site inhibitors for HIV-1 protease (HIV PR) and has l
ed to the design of a series of highly potent, C-2 symmetry-based, dio
l-containing inhibitors of HIV PR, one of which, A-77003, has reached
clinical trials. However, the stereochemistry of the diol core influen
ces protease inhibition and antiviral activity in a manner that is not
well understood. We analyzed the crystal structures of a diastereomer
ic series of C-2 symmetry-based diol inhibitors, along with a deshydro
xy analogue, bound to HIV PR and found that the stereochemistry of the
diol core influences the mode of binding to the active site aspartic
acids. Diasteromers with similar binding affinity can bind in differen
t, asymmetric and symmetric, modes, while those with different binding
affinities can bind in a similar manner. The positional symmetry of a
n inhibitor with respect to the enzyme C-2 axis may be distinguished f
rom its conformational symmetry. The structural differences between th
e inhibitor complexes were mainly confined to the central core portion
of the diols, can be described by torsional differences about the cen
tral three bonds, and primarily affect interactions within the active
site pocket formed by Asp 25/125 and Gly 27/127. Some flexibility in t
he enzyme backbone at Gly 127 was also apparent. Based on these result
s, we suggest that the binding mode for central hydroxy-bearing, C-2-s
ymmetric inhibitors will be determined by how well the inhibitor can s
imultaneously optimize hydrogen bonding with the active site carboxyla
te groups and van der Waals contacts with the neighboring backbone ato
ms of the active site ''psi''-loops. A symmetric hydrogen-bonding arra
ngement with either one or tio symmetrically positioned hydroxy groups
appears to be preferred over less symmetric configurations.