Abstract
Novel molecular function can be achieved by redesigning an enzyme’s active site so that it will perform its chemical reaction on a novel substrate. One of the main challenges for protein redesign is the efficient evaluation of a combinatorial number of candidate structures. The modeling of protein flexibility, typically by using a rotamer library of commonly-observed low-energy side-chain conformations, further increases the complexity of the redesign problem. A dominant algorithm for protein redesign is Dead-End Elimination (DEE), which prunes the majority of candidate conformations by eliminating rigid rotamers that provably are not part of the Global Minimum Energy Conformation (GMEC). The identified GMEC consists of rigid rotamers that have not been energy-minimized and is referred to as the rigid-GMEC. As a post-processing step, the conformations that survive DEE may be energy-minimized. When energy minimization is performed after pruning with DEE, the combined protein design process becomes heuristic, and is no longer provably accurate: That is, the rigid-GMEC and the conformation with the lowest energy among all energy-minimized conformations (the minimized-GMEC, or minGMEC) are likely to be different. While the traditional DEE algorithm succeeds in not pruning rotamers that are part of the rigid-GMEC, it makes no guarantees regarding the identification of the minGMEC. In this paper we derive a novel, provable, and efficient DEE-like algorithm, called minimized-DEE (MinDEE), that guarantees that rotamers belonging to the minGMEC will not be pruned, while still pruning a combinatorial number of conformations. We show that MinDEE is useful not only in identifying the minGMEC, but also as a filter in an ensemble-based scoring and search algorithm for protein redesign that exploits energy-minimized conformations. We compare our results both to our previous computational predictions of protein designs and to biological activity assays of predicted protein mutants. Our provable and efficient minimized-DEE algorithm is applicable in protein redesign, protein-ligand binding prediction, and computer-aided drug design.
Preview
Unable to display preview. Download preview PDF.
Similar content being viewed by others
References
Bolon, D., Mayo, S.: Enzyme-like proteins by computational design. Proc. Natl. Acad. Sci. USA 98, 14274–14279 (2001)
Cane, D., Walsh, C., Khosla, C.: Harnessing the biosynthetic code: combinations, permutations, and mutations. Science 282, 63–68 (1998)
Challis, G., Ravel, J., Townsend, C.: Predictive, structure-based model of amino acid recognition by nonribosomal peptide synthetase adenylation domains. Chem. Biol. 7, 211–224 (2000)
Conti, E., Stachelhaus, T., Marahiel, M., Brick, P.: Structural basis for the activation of phenylalanine in the non-ribosomal biosynthesis of Gramicidin S. EMBO J. 16, 4174–4183 (1997)
Cornell, W., Cieplak, P., Bayly, C., Gould, I., Merz, K., Ferguson, D., Spellmeyer, D., Fox, T., Caldwell, J., Kollman, P.: A second generation force field for the simulation of proteins, nucleic acids and organic molecules. J. Am. Chem. Soc. 117, 5179–5197 (1995)
Desmet, J., Maeyer, M., Hazes, B., Lasters, I.: The dead-end elimination theorem and its use in protein side-chain positioning. Nature 356, 539–542 (1992)
Doekel, S., Marahiel, M.: Dipeptide formation on engineered hybrid peptide synthetases. Chem. Biol. 7, 373–384 (2000)
Eppelmann, K., Stachelhaus, T., Marahiel, M.: Exploitation of the selectivity-conferring code of nonribosomal peptide synthetases for the rational design of novel peptide antibiotics. Biochemistry 41, 9718–9726 (2002)
Georgiev, I., Lilien, R., Donald, B.R.: A novel minimized dead-end elimination criterion and its application to protein redesign in a hybrid scoring and search algorithm for computing partition functions over molecular ensembles. Technical Report 570, Dartmouth Computer Science Dept. (2006), http://www.cs.dartmouth.edu/reports/abstracts/TR2006-570
Goldstein, R.: Efficient rotamer elimination applied to protein side-chains and related spin glasses. Biophys. J. 66, 1335–1340 (1994)
Gordon, D., Mayo, S.: Radical performance enhancements for combinatorial optimization algorithms based on the dead-end elimination theorem. J. Comput. Chem. 19, 1505–1514 (1998)
Hellinga, H., Richards, F.: Construction of new ligand binding sites in proteins of known structure: I. Computer-aided modeling of sites with pre-defined geometry. J. Mol. Biol. 222, 763–785 (1991)
Jaramillo, A., Wernisch, L., Héry, S., Wodak, S.: Automatic procedures for protein design. Comb. Chem. High Throughput Screen. 4, 643–659 (2001)
Jin, W., Kambara, O., Sasakawa, H., Tamura, A., Takada, S.: De novo design of foldable proteins with smooth folding funnel: Automated negative design and experimental verification. Structure 11, 581–591 (2003)
Keating, A., Malashkevich, V., Tidor, B., Kim, P.: Side-chain repacking calculations for predicting structures and stabilities of heterodimeric coiled coils. Proc. Natl. Acad. Sci. USA 98, 14825–14830 (2001)
Leach, A., Lemon, A.: Exploring the conformational space of protein side chains using dead-end elimination and the A* algorithm. Proteins 33, 227–239 (1998)
Lilien, R., Stevens, B., Anderson, A., Donald, B.R.: A novel ensemble-based scoring and search algorithm for protein redesign, and its application to modify the substrate specificity of the Gramicidin Synthetase A phenylalanine adenylation enzyme. Journal of Computational Biology 12(6–7), 740–761 (2005)
Looger, L., Dwyer, M., Smith, J., Hellinga, H.: Computational design of receptor and sensor proteins with novel functions. Nature 423, 185–190 (2003)
Lovell, S., Word, J., Richardson, J., Richardson, D.: The penultimate rotamer library. Proteins 40, 389–408 (2000)
Marvin, J., Hellinga, H.: Conversion of a maltose receptor into a zinc biosensor by computational design. PNAS 98, 4955–4960 (2001)
Mootz, H., Schwarzer, D., Marahiel, M.: Construction of hybrid peptide synthetases by module and domain fusions. Proc. Natl. Acad. Sci. USA 97, 5848–5853 (2000)
Najmanovich, R., Kuttner, J., Sobolev, V., Edelman, M.: Side-chain flexibility in proteins upon ligand binding. Proteins 39(3), 261–268 (2000)
Pierce, N., Spriet, J., Desmet, J., Mayo, S.: Conformational splitting: a more powerful criterion for dead-end elimination. J. Comput. Chem. 21, 999–1009 (2000)
Pierce, N., Winfree, E.: Protein design is NP-hard. Protein Eng. 15, 779–782 (2002)
Ponder, J., Richards, F.: Tertiary templates for proteins: use of packing criteria in the enumeration of allowed sequences for different structural classes. J. Mol. Biol. 193, 775–791 (1987)
Schneider, A., Stachelhaus, T., Marahiel, M.: Targeted alteration of the substrate specificity of peptide synthetases by rational module swapping. Mol. Gen. Genet. 257, 308–318 (1998)
Schwarzer, D., Finking, R., Marahiel, M.: Nonribosomal peptides: from genes to products. Nat. Prod. Rep. 20, 275–287 (2003)
Stachelhaus, T., Mootz, H., Marahiel, M.: The specificiy-conferring code of adenylation domains in nonribosomal peptide synthetases. Chem. Biol. 6, 493–505 (1999)
Stachelhaus, T., Schneider, A., Marahiel, M.: Rational design of peptide antibiotics by targeted replacement of bacterial and fungal domains. Science 269, 69–72 (1995)
Street, A., Mayo, S.: Computational protein design. Structure 7, R105–R109 (1999)
Weiner, S., Kollman, P., Case, D., Singh, U., Ghio, C., Alagona, G., Profeta, S., Weiner, P.: A new force field for molecular mechanical simulation of nucleic acids and proteins. J. Am. Chem. Soc. 106, 765–784 (1984)
Author information
Authors and Affiliations
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 2006 Springer-Verlag Berlin Heidelberg
About this paper
Cite this paper
Georgiev, I., Lilien, R.H., Donald, B.R. (2006). A Novel Minimized Dead-End Elimination Criterion and Its Application to Protein Redesign in a Hybrid Scoring and Search Algorithm for Computing Partition Functions over Molecular Ensembles. In: Apostolico, A., Guerra, C., Istrail, S., Pevzner, P.A., Waterman, M. (eds) Research in Computational Molecular Biology. RECOMB 2006. Lecture Notes in Computer Science(), vol 3909. Springer, Berlin, Heidelberg. https://doi.org/10.1007/11732990_44
Download citation
DOI: https://doi.org/10.1007/11732990_44
Publisher Name: Springer, Berlin, Heidelberg
Print ISBN: 978-3-540-33295-4
Online ISBN: 978-3-540-33296-1
eBook Packages: Computer ScienceComputer Science (R0)