Translation dynamics in human cells visualized at high resolution reveal cancer drug action
Author(s) -
Huaipeng Xing,
Reiya Taniguchi,
Iskander Khusainov,
Jan Philipp Kreysing,
Sonja Welsch,
Beata Turoňová,
Martin Beck
Publication year - 2023
Publication title -
science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 12.556
H-Index - 1186
eISSN - 1095-9203
pISSN - 0036-8075
DOI - 10.1126/science.adh1411
Subject(s) - ribosome , translation (biology) , internal ribosome entry site , homoharringtonine , biophysics , myeloid leukemia , chemistry , protein biosynthesis , microbiology and biotechnology , computational biology , biology , rna , biochemistry , messenger rna , cancer research , gene
Ribosomes catalyze protein synthesis by cycling through various functional states. These states have been extensively characterized in vitro, but their distribution in actively translating human cells remains elusive. We used a cryo-electron tomography-based approach and resolved ribosome structures inside human cells with high resolution. These structures revealed the distribution of functional states of the elongation cycle, a Z transfer RNA binding site, and the dynamics of ribosome expansion segments. Ribosome structures from cells treated with Homoharringtonine, a drug used against chronic myeloid leukemia, revealed how translation dynamics were altered in situ and resolve the small molecules within the active site of the ribosome. Thus, structural dynamics and drug effects can be assessed at high resolution within human cells.
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