Early nascent polypeptide dynamics are coupled to the flexibility of the ribosomal tunnel constriction
This study reveals that the ribosomal tunnel constriction, formed by proteins uL4 and uL22, functions as a dynamic flexible gate that adapts its width in response to nascent polypeptide presence, shifting from transient occlusion to accommodating helical structures, thereby influencing translocation, antibiotic action, and translation regulation.