Sparse Approximations Of Protein Structure From Noisy Random Projections
Single-particle electron microscopy is a modern technique that biophysicists employ to learn the structure of proteins. It yields data that consist of noisy random projections of the protein structure in random directions, with the added complication that the projection angles cannot be observed. In order to reconstruct a three-dimensional model, the projection directions need to be estimated by use of an ad-hoc starting estimate of the unknown particle. In this paper we propose a methodology that does not rely on knowledge of the projection angles, to construct an objective data-dependent low-resolution approximation of the unknown structure that can serve as such a starting estimate. The approach assumes that the protein admits a suitable sparse representation, and employs discrete L-1-regularization (LASSO) as well as notions from shape theory to tackle the peculiar challenges involved in the associated inverse problem. We illustrate the approach by application to the reconstruction of an E. coli protein component called the Klenow fragment.
Keywords: Statistical tomography ; electron microscopy ; single particles ; nearly black object ; Lasso ; deconvolution ; Roman surface ; Positron Emission Tomography ; Electron Cryomicroscopy ; Maximum-Likelihood ; Radon Shape ; Reconstruction ; Crystallography ; Regression ; Particles
Record created on 2012-06-25, modified on 2016-08-09