A transformation clustering algorithm and its application in polyribosomes structural profiling

Author:

Jiang Wenhong1,Wagner Jonathan23,Du Wenjing1,Plitzko Juergen4,Baumeister Wolfgang2,Beck Florian4,Guo Qiang15ORCID

Affiliation:

1. State Key Laboratory of Protein and Plant Gene Research, Peking-Tsinghua Center for Life Sciences, Academy for Advanced Interdisciplinary Studies, School of Life Sciences, Peking University , Beijing  100871, China

2. Department of Structural Molecular Biology, Max Planck Institute of Biochemistry , Am Klopferspitz 18,  82152 Martinsried, Germany

3. Department of Cellular Biochemistry, Max Planck Institute of Biochemistry , Am Klopferspitz 18,  82152 Martinsried, Germany

4. CryoEM Technology, Max Planck Institute of Biochemistry , Am Klopferspitz 18,  82152 Martinsried, Germany

5. Changping Laboratory , Beijing, China

Abstract

Abstract Improvements in cryo-electron tomography sample preparation, electron-microscopy instrumentations, and image processing algorithms have advanced the structural analysis of macromolecules in situ. Beyond such analyses of individual macromolecules, the study of their interactions with functionally related neighbors in crowded cellular habitats, i.e. ‘molecular sociology’, is of fundamental importance in biology. Here we present a NEighboring Molecule TOpology Clustering (NEMO-TOC) algorithm. We optimized this algorithm for the detection and profiling of polyribosomes, which play both constitutive and regulatory roles in gene expression. Our results suggest a model where polysomes are formed by connecting multiple nonstochastic blocks, in which translation is likely synchronized.

Funder

Peking-Tsinghua Center for Life Sciences

School of Life Sciences (SLS) of Peking University

State Key Laboratory of Protein and Plant Gene Research

Publisher

Oxford University Press (OUP)

Subject

Genetics

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