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2001-2002
2002-2003
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Alexander Grosberg
Date: September 9
Time: Noon to 1
Place: BSBE 4-101
We design toy protein mimicking a machine-like function of an
enzyme. Using an insight gained by the study of conformation
space of compact lattice polymers, we demonstrate the possibility
of a large scale conformational rearrangement which occurs (i)
without opening a compact state, and (ii) along a linear
(one-dimensional) pathway.
We also demonstrate the possibility
to extend sequence design method such that it yields a "collective
funnel" landscape in which the toy protein (computationally) folds
into the valley with rearrangement pathway at its bottom. Energies
of the states along the pathway can be designed to be about equal,
allowing for diffusion along the pathway. They can also be
designed to provide for a significant bias in one certain
direction, in which case toy protein acts as a spring capable to
accumulate energy without dissipation.
Together with a toy ligand
molecule, our "enzimatic" machine can perform the entire cycle,
including conformational relaxation in one direction upon ligand
binding and conformational relaxation in the opposite direction
upon ligand release. This model, however schematic, should be
useful as a test ground for phenomenological theories of
machine-like properties of enzymes.
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