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Exact reaction coordinates for flap opening in HIV-1 protease
Exact reaction coordinates for flap opening in HIV-1 protease
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Exact reaction coordinates for flap opening in HIV-1 protease
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Exact reaction coordinates for flap opening in HIV-1 protease
Exact reaction coordinates for flap opening in HIV-1 protease

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Exact reaction coordinates for flap opening in HIV-1 protease
Exact reaction coordinates for flap opening in HIV-1 protease
Journal Article

Exact reaction coordinates for flap opening in HIV-1 protease

2022
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Overview
The primary goal of protein science is to understand how proteins function, which requires understanding the functional dynamics responsible for transitions between different functional structures of a protein. A central concept is the exact reaction coordinates that can determine the value of committor for any protein configuration, which provide the optimal description of functional dynamics. Despite intensive efforts, identifying the exact reaction coordinates (RCs) in complex molecules remains a formidable challenge. Using the recently developed generalized work functional, we report the discovery of the exact RCs for an important functional process—the flap opening of HIV-1 protease. Our results show that this process has six RCs, each one is a linear combination of ~240 backbone dihedrals, providing the precise definition of collectivity and cooperativity in the functional dynamics of a protein. Applying bias potentials along each RC can accelerate flap opening by 10³ to 10⁴ folds. The success in identifying the RCs of a protein with 198 residues represents a significant progress beyond that of the alanine dipeptide, currently the only other complex molecule for which the exact RCs for its conformational changes are known. Our results suggest that the generalized work functional (GWF) might be the fundamental operator of mechanics that controls protein dynamics.