Colloquium: Geometrical approach to protein folding: a tube picture
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Publication:3077097
DOI10.1103/REVMODPHYS.75.23zbMATH Open1205.92019arXivcond-mat/0301220OpenAlexW1789357798MaRDI QIDQ3077097FDOQ3077097
Authors: Jayanth R. Banavar, Amos Maritan
Publication date: 21 February 2011
Published in: Reviews of Modern Physics (Search for Journal in Brave)
Abstract: A framework is presented for understanding the common character of proteins. Proteins are linear chain molecules. However, the simple model of a polymer viewed as spheres tethered together does not account for many of the observed characteristics of protein structures. The authors show here that proteins may be regarded as tubes of nonzero thickness. This approach allows one to bridge the conventional compact polymer phase with a novel phase employed by Nature to house biomolecular structures. The continuum description of a tube (or a sheet) of arbitrary thickness entails using appropriately chosen many-body interactions rather than two-body interactions. The authors suggest that the structures of folded proteins are selected based on geometrical considerations and are poised at the edge of compaction, thus accounting for their versatility and flexibility. This approach also offers an explanation for why helices and sheets are the building blocks of protein structures.
Full work available at URL: https://arxiv.org/abs/cond-mat/0301220
Cites Work
Cited In (7)
- Helices for mathematical modelling of proteins, nucleic acids and polymers
- Folding of proteins in Go models with angular interactions
- Dynamical models of molecular chains and efficient integration algorithms
- On the number of tubes touching a sphere or a tube
- Langevin dynamics simulations reveal biologically relevant folds arising from the incorporation of a torsional potential
- A comment on the protein folds as platonic forms
- Functionals linear in curvature and statistics of helical proteins
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