Cryo-EM structure of the ancient eukaryotic ribosome from the human parasite Giardia lamblia

Author:

Hiregange Disha-Gajanan1,Rivalta Andre1,Bose Tanaya1,Breiner-Goldstein Elinor1,Samiya Sarit1,Cimicata Giuseppe1,Kulakova Liudmila2,Zimmerman Ella1,Bashan Anat1ORCID,Herzberg Osnat23,Yonath Ada1

Affiliation:

1. Department of Chemical and Structural Biology, Weizmann Institute of Science, Rehovot 7610001, Israel

2. Institute for Bioscience and Biotechnology Research, University of Maryland, Rockville, MD 20742-4454, USA

3. Department of Chemistry and Biochemistry, University of Maryland, College Park, MD 20742-4454, USA

Abstract

Abstract Giardiasis is a disease caused by the protist Giardia lamblia. As no human vaccines have been approved so far against it, and resistance to current drugs is spreading, new strategies for combating giardiasis need to be developed. The G. lamblia ribosome may provide a promising therapeutic target due to its distinct sequence differences from ribosomes of most eukaryotes and prokaryotes. Here, we report the cryo-electron microscopy structure of the G. lamblia (WB strain) ribosome determined at 2.75 Å resolution. The ribosomal RNA is the shortest known among eukaryotes, and lacks nearly all the eukaryote-specific ribosomal RNA expansion segments. In contrast, the ribosomal proteins are typically eukaryotic with some species-specific insertions/extensions. Most typical inter-subunit bridges are maintained except for one missing contact site. Unique structural features are located mainly at the ribosome’s periphery. These may be exploited as target sites for the design of new compounds that inhibit selectively the parasite’s ribosomal activity.

Funder

Kimmelman Center for Macromolecular Assemblies

National Institutes of Health

Kimmelman Center for Structural Biology

Publisher

Oxford University Press (OUP)

Subject

Genetics

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