Single-particle electron cryomicroscopy (cryo-EM) is a method for observing the three- dimensional structures of large macromolecules. In cryo-EM the experimental data consist of noisy, random projection images of macromolecular """"""""particles"""""""", and the problem is finding the 3D structure which is consistent with these images. The proposal aims to develop and apply to experimental data novel algorithms for solving two difficult mathematical problems posed by this technique of structural biology. First, classical cryo-EM reconstruction techniques assume that the particles are identical. However, in many datasets this assumption does not hold. Some molecules of interest have more than one conformational state. These structural variations are of great interest to biologists, as they provide insight int the functioning of the molecule. The first area of investigation in this project is the development of algorithmic and mathematical framework for determining structures associated with heterogeneous particle populations. The proposed algorithm is not only faster than existing techniques but is also mathematically provable to reveal the different conformations if the number of images is sufficiently large. Second, a major limiting factor for present cryo-EM studies is the particle size. Images of small particles are often too noisy for existing methods to provide valid three-dimensional reconstructions;although the images contain structural information, the assignment of orientations to the individual particles is unreliable. The second area of investigation focuses on developing a radical new approach for reconstruction of small particles without the need for determining particle orientations.

Public Health Relevance

Determining the structures of proteins and other large molecules is an essential step in the basic understanding of biological processes, and a first step in rational drug design. We propose to develop new, faster and more reliable computer algorithms to significantly increase the power of structure-determination using cryo-EM.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
2R01GM090200-06
Application #
8761618
Study Section
Macromolecular Structure and Function D Study Section (MSFD)
Program Officer
Flicker, Paula F
Project Start
2009-08-01
Project End
2018-06-30
Budget Start
2014-08-01
Budget End
2015-06-30
Support Year
6
Fiscal Year
2014
Total Cost
Indirect Cost
Name
Princeton University
Department
Biostatistics & Other Math Sci
Type
Schools of Arts and Sciences
DUNS #
City
Princeton
State
NJ
Country
United States
Zip Code
08543
Andén, Joakim; Singer, Amit (2018) Structural Variability from Noisy Tomographic Projections. SIAM J Imaging Sci 11:1441-1492
Bendory, Tamir; Boumal, Nicolas; Ma, Chao et al. (2018) Bispectrum Inversion with Application to Multireference Alignment. IEEE Trans Signal Process 66:1037-1050
Heimowitz, Ayelet; Andén, Joakim; Singer, Amit (2018) APPLE picker: Automatic particle picking, a low-effort cryo-EM framework. J Struct Biol 204:215-227
Greenberg, Ido; Shkolnisky, Yoel (2017) Common lines modeling for reference free Ab-initio reconstruction in cryo-EM. J Struct Biol 200:106-117
Abbe, Emmanuel; Pereira, João M; Singer, Amit (2017) Sample Complexity of the Boolean Multireference Alignment Problem. Proc IEEE Int Symp Info Theory 2017:1316-1320
Bhamre, Tejal; Zhao, Zhizhen; Singer, Amit (2017) MAHALANOBIS DISTANCE FOR CLASS AVERAGING OF CRYO-EM IMAGES. Proc IEEE Int Symp Biomed Imaging 2017:654-658
Zhang, Teng; Singer, Amit (2017) Disentangling orthogonal matrices. Linear Algebra Appl 524:159-181
Landa, Boris; Shkolnisky, Yoel (2017) Steerable Principal Components for Space-Frequency Localized Images. SIAM J Imaging Sci 10:508-534
Bhamre, Tejal; Zhang, Teng; Singer, Amit (2016) Denoising and covariance estimation of single particle cryo-EM images. J Struct Biol 195:72-81
Pragier, Gabi; Greenberg, Ido; Cheng, Xiuyuan et al. (2016) A Graph Partitioning Approach to Simultaneous Angular Reconstitution. IEEE Trans Comput Imaging 2:323-334

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