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Biophys J, January 2001, p. 505-515, Vol. 80, No. 1


and
*School of Engineering and Polymer Research Center, Bogazici
University, and TUBITAK Advanced Polymeric Materials Research Center,
Bebek 80815, Istanbul, Turkey; and
Molecular Structure
Section, Laboratory of Experimental and Computational Biology, Division
of Basic Sciences, National Cancer Institute and Science Applications
International Corp., National Institutes of Health, Bethesda and
Frederick, Maryland 20892-5677 USA
Fluctuations about the native conformation of proteins
have proven to be suitably reproduced with a simple elastic network model, which has shown excellent agreement with a number of different properties for a wide variety of proteins. This scalar model simply investigates the magnitudes of motion of individual residues in the
structure. To use the elastic model approach further for developing the
details of protein mechanisms, it becomes essential to expand this
model to include the added details of the directions of individual residue fluctuations. In this paper a new tool is presented for this
purpose and applied to the retinol-binding protein, which indicates
enhanced flexibility in the region of entry to the ligand binding site
and for the portion of the protein binding to its carrier protein.
Biophys J, January 2001, p. 505-515, Vol. 80, No. 1
© 2001 by the Biophysical Society 0006-3495/01/01/505/11 $2.00
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