DNA replication has been reconstituted in vitro with yeast proteins, and the minimal system requires the coordinated assembly of 16 distinct replication factors, consisting of 42 polypeptides. To understand the molecular interplay between these factors at the single residue level, new structural biology tools are being developed. Inspired by advances in singlemolecule fluorescence imaging and cryo-tomography, novel single-particle cryo-EM experiments have been used to characterise the structural mechanism for the loading of the replicative helicase. Here, we discuss how in silico reconstitution of single-particle cryo-EM data can help describe dynamic systems that are difficult to approach with conventional three-dimensional classification tools.
机构:
Department of Biochemistry and Molecular Biology and the Huck Institutes of the Life Sciences,Pennsylvania State UniversityDepartment of Biochemistry and Molecular Biology and the Huck Institutes of the Life Sciences,Pennsylvania State University
Jean-Paul Armache
Yifan Cheng
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Howard Hughes Medical Institute, University of California San Francisco
Department of Biochemistry and Biophysics,University of California San FranciscoDepartment of Biochemistry and Molecular Biology and the Huck Institutes of the Life Sciences,Pennsylvania State University
机构:
Univ Calif San Francisco, Dept Biochem & Biophys, San Francisco, CA 94158 USAUniv Calif San Francisco, Dept Biochem & Biophys, San Francisco, CA 94158 USA
机构:
Penn State Univ, Dept Biochem & Mol Biol, University Pk, PA 16802 USA
Penn State Univ, Huck Inst Life Sci, University Pk, PA 16802 USAPenn State Univ, Dept Biochem & Mol Biol, University Pk, PA 16802 USA
Armache, Jean-Paul
Cheng, Yifan
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机构:
Univ Calif San Francisco, Howard Hughes Med Inst, San Francisco, CA 94143 USA
Univ Calif San Francisco, Dept Biochem & Biophys, San Francisco, CA 94143 USAPenn State Univ, Dept Biochem & Mol Biol, University Pk, PA 16802 USA