Award details

Mining of protein data bank and feedback to X-ray crystal structure solution and analysis

Reference	BB/F001134/1
Principal Investigator / Supervisor	Dr Garib Murshudov
Co-Investigators / Co-Supervisors	Professor Keith Wilson
Institution	University of York
Department	Chemistry
Funding type	Research
Value (£)	254,699
Status	Completed
Type	Research Grant
Start date	01/02/2008
End date	31/01/2011
Duration	36 months

Abstract

The aim is to advance the application of modern statistical techniques to macromolecular crystallography, and hence extend its application to more challenging structural biological macromolecular crystallographic analysis. There are two main objectives: 1) statistical treatment of order-disorder (OD) structures and 2) design and use of prior structural knowledge. Both objectives will be achieved in three stages: 1) analyse, extract and classify the relevant information from structures in the PDB; 2) use this information to design probability distributions that best describes their behaviour and 3) apply the resulting software to challenging crystal structure analysis. The objectives will be achieved as follows: 1)The PDB will be analysed and entries with 'crystal' imperfections such as (OD) structures with and without twinning will be extracted. These structures will be classified and likelihood functions be designed to deal with such problems. The resulting software will be calibrated using all entries in the PDB. Software will be designed to correct the space group of crystals during refinement and feed the results back into both the data processing and refinement steps. 2)The PDB will be analysed and information about internal degrees of freedom of macromolecules will be extracted. Prior probability distributions of inter-atomic distances of atoms will be designed. To take into account correlated motion of atoms in molecules, differences of atomic displacement parameters will be analysed and appropriate probability distributions will be designed. These will allow refining structures at low resolution. Such restraints will allow smooth transition from rigid group to all-atom models, extracting the optimal information from data while retaining the structural integrity of the derived model. All developed algorithms either will be implemented in the programs REFMAC or MOLREP, or in new software. The software will be made available to the community via CCP4.

Summary

The aim is to improve the computer software used in determining the 3-D structures of complex biological molecules which make up living organisms. These molecules are coded for by a 'blueprint', in the form of a DNA sequence in the genome, which describes how to make them. Due to enormous advances in molecular biology, a number of projects, including the Human Genome Project, have led to the determination of the complete DNA sequences of a number of organisms. We can therefore read the plans for many of the molecules of life. However without knowledge of their 3-D structure, it is very hard to understand how they actually work. Understanding this is an important step in fixing them when they go wrong, and therefore, in curing a range of illnesses as well as using such molecules in a range of applications in biotechnology. The solution to this problem is through Structural Biology, in which the molecules are manufactured on the basis of their blueprints and 3-D models are constructed for them usually using X-ray crystallography. This allows pictures to be made of biological molecules in which individual atoms can be identified. Crystallography is analogous to the use of a microscope to magnify objects, which are smaller than can seen with the naked eye. However, even the optical microscope has limitations, and we cannot see objects which are smaller than the wavelength of light, roughly 1 millionth of a metre. Atoms are about 1000 times small than this, and we need to use X-rays, which have a wavelength about the same as the size of the atoms, in order to see them. Unfortunately structure solution by X-ray crystallography is complicated because unlike the optical microscope, there is no lens system for X-rays and we need to carry out a number of challenging experiments followed by complex computation and problem solving by experienced scientists. This is especially complex when we look at crystals of proteins, which are actually imperfect and contain about 50% water. The aim of this project is to improve some of the key computational tools of crystallography to make this task easier and more automatic, and to allow the solution of more difficult problems. The basic problem lies in the low observation to parameter ration in protein crystallography (equivalent to a low signal-to-noise ratio in image recognition). Advanced statistical methods are required to make the best use of the limited data available.

Committee	Closed Committee - Biomolecular Sciences (BMS)
Research Topics	Structural Biology, Technology and Methods Development
Research Priority	X – Research Priority information not available
Research Initiative	X - not in an Initiative
Funding Scheme	X – not Funded via a specific Funding Scheme

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