A fast, accurate system for quickly solving stubborn RNA structures


Credit: SLAC National Accelerator Laboratory
Credit: SLAC National Accelerator Laboratory

The single-stranded genetic material RNA is best known for guiding the assembly of proteins in our cells and carrying the genetic code for viruses like SARS-CoV-2 and HIV. But 40 years ago, scientists discovered another hidden talent: It can catalyze chemical reactions in the cell, including snipping and joining RNA strands. This gave new momentum to the idea that RNA was the driving force behind the evolution of large molecules that ultimately led to life.


While scientists have learned a lot since then, they haven't been able to get 3D images of naked RNA molecules in high enough resolution to see all the pockets and folds and other structures that are key to understanding how they function. The molecules are like fidgety kids with floppy arms that won't hold still for a photo unless they're part of a larger molecular complex that pins them in place.


A new system developed at Stanford University and the Department of Energy's SLAC National Accelerator Laboratory solves that problem. It combines computer software and cryogenic electron microscopy, or cryo-EM, to determine the 3D structures of RNA-only molecules with unprecedented speed, accuracy, and resolution.


In two new studies, the research team led by SLAC/Stanford Professor Wah Chiu and Stanford Professor Rhiju Das push the resolution of the technique to as high as 3.1 angstroms just shy of the point where individual atoms become visible and apply it to two RNA structures that are of profound interest to scientists.


The first study, published in Nature today, reveals the first full-length, near-atomic structure of a catalytic RNA, or ribozyme, from a one-celled creature called Tetrahymena that lives in pond scum. It was the first ribozyme ever discovered and has served as a sort of lab rat for studying ribozymes ever since.


The second, which has been posted as a preprint, reveals tiny pockets in a bit of RNA from SARS-CoV-2 called the frameshift stimulation element or FSE. It subtly tricks infected cells into making alternative sets of viral proteins and plays such an important role in the virus's ability to replicate that it remains the same even when other parts of the virus mutate to create new variants. This makes it a good potential target for drugs to treat COVID-19, its variants, and maybe even other coronaviruses, and a number of research groups have been exploring that possibility.


The FSE study was carried out in 2020, at a time when SLAC and Stanford were shut down due to the pandemic, and only essential work related to the coronavirus response was allowed.


Guided by insights from their 3D structure of FSE, Das's team and collaborators in Professor Jeff Glenn's lab at Stanford engineered DNA molecules that pair up with a strategic region of the FSE and disrupt its structure.

While researchers are very far from demonstrating that such a molecule could thwart viral infection in humans, the study does identify a potential path for eventually developing a treatment, the scientists said.


Das said, we don't know what the next pandemic virus will be, but we're pretty confident it will be a single-strand RNA virus transmitted from animals to humans, and it will likely have a few bits of RNA that resist mutation. With this accelerated system we've developed, it now seems feasible to study viruses found in humans or animals, look for those conserved bits, quickly determine their 3D RNA structures and develop antivirals against them.


The two scientists started collaborating in 2017 after Das heard Chiu give a talk on using cryo-EM to solve the structure of RNA molecules.


Das said, it blew me away. I had fallen in love with RNA in 2001. I thought it was the most important molecule of life. The first RNA molecule I looked at was this Tetrahymena ribozyme. Many, many people had worked on it was a bit of a cult molecule and I spent five years of my Ph.D. work trying to understand how it folds. So after hearing Wah's talk I suggested that we work together to determine its structure. As far as scientists can tell, the ribozyme has no biological function in Tetrahymena. It's an inconsequential molecule in what some might consider an inconsequential organism. But 40 years ago, when Thomas Cech discovered that this tiny piece of RNA could cut itself out of a Tetrahymena RNA strand, paste the two loose ends together and float away, it was this magical thing that no one expected an RNA strand to do on its own. They immediately realized that this piece of RNA must be a little multistep machine, a catalyst. Cech shared the 1989 Nobel Prize in Chemistry for the discovery.


Chiu had begun a similar love affair with cryo-EM as a graduate student at the University of California, Berkeley in the 1970s. Now the founding co-director of the Stanford-SLAC Cryo-EM Facilities, where the imaging for these studies was done, he has devoted his career to honing the technique and using it to examine cells and the molecular machines inside them in finer and finer detail not just to see smaller things but to understand how they function and interact with each other.


Chiu said, it's been a dream of mine to use cryo-EM to study RNA in all its forms. I consider getting these RNA structures one of my top accomplishments. If we can do this with one molecule, in theory, we can do it with many others.


Das and Chiu's work builds on Ribosolve, a pipeline their groups developed in the two years prior to the pandemic that allows them to quickly solve the structures of RNAs one right after another, more reliably and in much more detail than before. It combines computational tools developed by Stanford Ph.D. student Kalli Kappel with chemical mapping tools from the Das lab and cryo-EM imaging advances from postdoctoral researchers Kaiming Zhang and Zhaoming Su.


In a paper in Nature Methods last year, the team reported using the new approach to determine the 3D structures of the Tetrahymena ribozyme and 10 other RNA molecules with better than 10-angstrom resolution.


wrote Jane S. Richardson, a professor of biochemistry at Duke University in a commentary that accompanied the report, each of these 11 new structures turned out to provide biological or biochemical insights. She called the approach a groundbreaking new method" that produces fast and reliable structures of RNA-only molecules that were not considered feasible before and added that increasing the resolution to 2-4 angstroms would be a desirable demonstration of its usefulness for both RNA and proteins.


In their new Nature paper, the team reports that it has now achieved that higher resolution for the Tetrahymena ribozyme and is hoping to push toward it for FSE, with the ultimate goal of producing atomic-resolution structures for these and potentially thousands of other RNAs.


Das said, I do think the Ribosolve pipeline has the potential to transform our understanding of these molecules, and maybe our ability to develop medicines, too. This couldn't have happened anywhere else. Having access to world-class cryo-EM instruments was key, along with meeting someone like Wah who shared our intuition that this could be important.



Journal Information:  Zhaoming Su et al, Cryo-EM structures of full-length Tetrahymena ribozyme at 3.1 Å resolution, Nature (2021). DOI: 10.1038/s41586-021-03803-w

Kaiming Zhang et al, Cryo-electron Microscopy and Exploratory Antisense Targeting of the 28-kDa Frameshift Stimulation Element from the SARS-CoV-2 RNA Genome, bioRxiv (2020). DOI: 10.1101/2020.07.18.209270

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