Cryo-EM structures reveal high-resolution mechanism of a DNA polymerase sliding clamp loader

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Publikace nespadá pod Filozofickou fakultu, ale pod Středoevropský technologický institut. Oficiální stránka publikace je na webu muni.cz.
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GAUBITZ Christl LIU Xingchen PAJAK Joshua STONE Nicholas P HAYES Janelle A DEMO Gabriel KELCH Brian A

Rok publikování 2022
Druh Článek v odborném periodiku
Časopis / Zdroj elife
Fakulta / Pracoviště MU

Středoevropský technologický institut

Citace
www https://elifesciences.org/articles/74175
Doi http://dx.doi.org/10.7554/eLife.74175
Klíčová slova sliding clamp loader; AAA plus; DNA replication; S; cerevisiae
Popis Sliding clamps are ring-shaped protein complexes that are integral to the DNA replication machinery of all life. Sliding clamps are opened and installed onto DNA by clamp loader AAA+ ATPase complexes. However, how a clamp loader opens and closes the sliding clamp around DNA is still unknown. Here, we describe structures of the Saccharomyces cerevisiae clamp loader Replication Factor C (RFC) bound to its cognate sliding clamp Proliferating Cell Nuclear Antigen (PCNA) en route to successful loading. RFC first binds to PCNA in a dynamic, closed conformation that blocks both ATPase activity and DNA binding. RFC then opens the PCNA ring through a large-scale ‘crab-claw’ expansion of both RFC and PCNA that explains how RFC prefers initial binding of PCNA over DNA. Next, the open RFC:PCNA complex binds DNA and interrogates the primer-template junction using a surprising base-flipping mechanism. Our structures indicate that initial PCNA opening and subsequent closure around DNA do not require ATP hydrolysis, but are driven by binding energy. ATP hydrolysis, which is necessary for RFC release, is triggered by interactions with both PCNA and DNA, explaining RFC’s switch-like ATPase activity. Our work reveals how a AAA+ machine undergoes dramatic conformational changes for achieving binding preference and substrate remodeling.
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