Mitoribosomes are nano particles essential for the synthesis and maintenance of bioenergetic proteins that produce more than 90 percent of our energy to support a human life. Eight years ago, the term “Resolution Revolution” was coined in relation to the first structure determination of the mitoribosome. Its intricate structure consists of over 80 different components, and more recent structural studies have further deepened our understanding of the mitoribosome structure, function, and antibiotic binding. However, we still lack information on the assembly of the mitoribosomal components that would explain how they cooperatively become to be the mitoribosome that is capable to initiate a protein synthesis. This is particularly important as defects in the assembly are linked to severe pathologies that manifest as a broad range of developmental disorders.

The paper published in Nature presents a cryo-EM analysis of assembly intermediates that explains how action of step-specific factors modulate the dynamic mechanism of biogenesis and establishes the catalytic mitoribosome that can activate our metabolism.

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The data reveals a model for the progression through a multistep assembly pathway that includes a sequence of binding factors as an integrated network. The progression is controlled via an allosteric mechanism to promote a regulated and gradual maturation. The high resolution allowed to reveal how a premature binding of genetic material is blocked and also to detect essential gentle modifications that occur on the mitoribosomal core at each of the assembly steps.

Intriguingly, previously known as “initiation" factor mtIF3 binds already during the assembly, and a unique protein mS37 then disrupts its contact, which marks the completion of the assembly and the initiation of protein synthesis. Thus, the study features a new paradigm of a single protein that links the process of the assembly to the catalytic function of the mitoribosome that is capable of producing metabolic energizers for our cells.

- This press release was provided by the Science For Life Laboratory