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Title page for ETD etd-07022015-151149

Type of Document Dissertation
Author DeLuca, Samuel Louis
Author's Email Address samuel.l.deluca@gmail.com
URN etd-07022015-151149
Title Development of Novel Methods for Computational Protein Design and Protein-Ligand Docking
Degree PhD
Department Chemical and Physical Biology
Advisory Committee
Advisor Name Title
Terry Lybrand Committee Chair
Brian Bachmann Committee Member
Heidi Hamm Committee Member
Stephen Fesik Committee Member
  • RosettaScripts
  • RosettaDesign
  • protein design
  • machine learning
  • Docking
  • Protein-Ligand Docking
  • Rosetta
Date of Defense 2015-05-06
Availability unrestricted
The ability to make rapid predictions of macro-molecular structures will enable researchers to carry out effective protein design, virtual High Throughput Screening (vHTS) and rational drug design studies. Here, we describe the development of several new methods in the service of these aims. Specifically, a novel energy term for protein design was implemented and optimized as part of the Rosetta molecular modeling suite. This energy term is based on a statistical analysis of experimental protein structural data, and aims to produce more native-like protein designs. Additionally, a new sampling algorithm and scoring function for the RosettaLigand protein-ligand docking tool was implemented. The new sampling algorithm results in a 30-fold increase in docking speed, and a 15% improvement in success rate across a wide range of protein systems. The new scoring function consists of a set of cartesian grids representing shape complementarity, hydrogen bonding, and ligand microenvironment environment properties. RosettaLigand docking predictions and scores were then combined with chemical descriptor information and used as the input to train a set of neural networks predicting ligand binding affinity. While the resulting networks did exhibit the ability to make predictions more effectively than RosettaLigand alone in a cross-validation study, the models were insufficiently general to make effective predictions when applied to a challenging, independent benchmarking set.

In addition to these new methods, appendix chapters detail the results of a ligand docking study into potential drug candidates targeting both RPA70 and MgluR5, an analysis of the limitations of the Rosetta atom typing system with respect to ligand parameterization, descriptions of a number of new software tools for the analysis of large protein datasets, and documentation of the protocols necessary to recapitulate the scientific studies reported here. In total, this work represents a substantial improvement in the overall performance of RosettaLigand, and provides numerous avenues for further research and development.

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