Decoding the identity of biomolecules from trace samples is a longstanding goal in the field of biotechnology, and while next-generation sequencing technologies have made it possible to identify individual DNA and RNA molecules, the same capability isn’t yet available for proteins. But scientists working at the Molecular Robotics Initiative within the Wyss Institute at Harvard University, the Blavatnik Institute at Harvard Medical School (HMS), and Boston Children’s Hospital (BCH) have now used DNA to create what they say may be the world’s tiniest ruler for measuring proteins.
Dubbed “DNA Nanoswitch Calipers” (DNC), the technology enables researchers to perform distance measurements on single peptides with high precision, by applying small amounts of force. By rapidly making many of these distance measurements on the same molecule, DNC creates a unique “fingerprint” that can be used to identify the same molecule in subsequent experiments.
“When you’re trying to understand something in biology, there are two main methods of inquiry: you can observe your subject in its natural state, or you can perturb it and see how it reacts,” said Wesley Wong, PhD, an associate faculty member at the Wyss Institute and associate professor at HMS who is also an investigator at BCH. “Observations can provide lots of great biological information, but sometimes the best way to learn about something is to physically interact with it. Determining the pattern of amino acids within a peptide molecule by applying force is a new paradigm in the ongoing scientific quest for techniques that will enable us to sequence proteins as easily as we currently sequence DNA.”
Wong is corresponding author of the team’s published paper in Nature Nanotechnology, titled, “Single-molecule mechanical fingerprinting with DNA nanoswitch calipers.”
Proteins are critically important players in nearly all biological processes, but these molecules are much more complex than DNA and RNA, and are often chemically modified, making the identification of single proteins within a sample—single-molecule proteomics—challenging. “Advances in DNA analysis have substantially affected clinical practice and basic research, but corresponding developments for proteins face challenges due to their relative complexity and our inability to amplify them,” the authors wrote. “A method for accurately and comprehensively analyzing proteins within trace samples would affect fields ranging from diagnostics to cell biology, but remains a highly challenging goal … Despite progress in methods such as mass spectrometry and mass cytometry, single-molecule protein identification remains a highly challenging objective.”
DNC is based on the underlying technology of the DNA nanoswitch. This is, effectively, a single strand of DNA with molecular “handles” attached to it at multiple points along its length. When two of these handles bind to each other, they create a loop in the DNA strand, and the overall length of the strand is shortened. When force is applied to pull the handles apart, the strand extends back to its original length. The difference between the length of the strand in its looped and unlooped states reflects the size of the loop, and thus the distance between the handles.
The research team realized that they could take DNA nanoswitches one step further. If they instead engineered the handles to bind to a biomolecule, the handles could effectively “pinch” the molecule between themselves like the two tips of a caliper, rather than binding to each other. By measuring how the addition of the target molecule between the handles changed the overall length of the DNA nanoswitch in looped vs. unlooped states, the team hypothesized that they could effectively measure the size of the molecule.
“In some ways, DNA nanoswitches harness one of the most classical, mechanical methods for measuring objects: just apply force to something and see how it changes in response,” said co-first author Darren Yang, PhD, a postdoctoral researcher at the Wyss Institute and BCH. “It’s an approach that we haven’t really seen used in the field of single-molecule proteomics, because applying force to such small objects is incredibly challenging. But we were up to the challenge.”
To turn their idea of a new, force-based measuring technique into reality, Yang and colleagues first attached two different types of handles to a target molecule: one “strong” handle to firmly anchor the molecule to one end of the DNC, and several “weak” handles that could attach to the other end of the DNC. They then tethered both ends of the DNC to two optically trapped beads suspended in laser beams. By moving the beads closer together, they induced one of the target molecule’s weak handles to bind to the DNC, creating a looped state. When they then increased the force by moving the beads further apart, the weak handle eventually released its bond, returning the DNC to its longer, unlooped state.”
“DNA nanoswitches are tethers of DNA decorated at specific sites with functionalities that can bind—either directly to each other or through a third bridging complex,” the authors explained. “Binding causes a section of the nanoswitch to loop out, shortening the tether length; when these bonds break, the tether extends back to its original length … Essentially, the change in length from a looped to an unlooped configuration reflects the size of the molecular bridge that closes the loop—the larger the bridge, the smaller the change in length.”
The team first tested the DNC technology on simple, single-stranded DNA (ssDNA) molecules, and confirmed that the change in distance measurements between the DNC’s looped and unlooped state directly correlated with the length of the target molecule. These length changes could be measured with angstrom-level precision (that’s ten times smaller than the width of a DNA double helix), enabling the identification of changes in length as small as that of a single nucleotide.
Because the target molecule contains multiple weak handles that can bind to the DNC, repeated cycles of binding and breaking those handles creates a series of distance measurements between the strong handle and the weak handles that are unique to each molecule measured. This “fingerprint” can be used to identify a known molecule within a sample, or to infer structural information about an unknown molecule.
Having confirmed that DNC could reliably measure the size of DNA molecules, the researchers shifted focus to proteins. They designed a synthetic peptide with a known length and sequence and repeated the experiment, attaching it to one end of the DNC via the strong handle and repeatedly attaching and breaking the bonds between its weak handles and the DNC by applying different amounts of force.
They found that all of the distances their tool measured between the strong and weak handles matched the distances expected based on the length of the DNC and the lengths of the amino acids in the peptide. They also got similar results when they used the DNC to measure a naturally occurring linearized peptide called NOXA BH3.
This process also generated unique measurement fingerprints for each peptide. “Performing multiple distance measurements on a single molecule enables the creation of a mechanical fingerprint that can be used for protein identification …” they wrote. The team created a computer model to predict how many human proteins could be uniquely identified using this method, and found that over 75% of the proteins in a commonly used protein database could be identified via fingerprints, with a probability of at least 90%.
“We were actually somewhat surprised by how well this technique worked,” said co-first author Prakash Shrestha, PhD, a postdoctoral fellow at the Wyss Institute and BCH. “Optical tweezers have been around for decades and cycling DNA between a looped and unlooped state has been around for about 10 years, and we weren’t sure whether we could get sufficiently high-resolution measurements by combining those ideas. But it turned out that these fingerprints are very effective for identifying proteins.”
Identifying single protein molecules is an impressive feat itself, but being able to do that for multiple proteins simultaneously is the true holy grail for single-molecule proteomics. The team further demonstrated that by replacing the optical beads with a magnetic tweezer system, they were able to perform measurements on multiple different peptides in parallel, as well as determine the relative concentrations of different molecules. “Using optical tweezers, we demonstrate absolute distance measurements with ångström-level precision for both DNA and peptides, and using multiplexed magnetic tweezers, we demonstrate quantification of relative abundance in mixed samples,” they wrote.
“We have also demonstrated how throughput can be increased through parallelization, by implementing this assay on a multiplexed magnetic tweezers system. This enabled us to measure the relative concentrations of different ratios of peptides within a heterogeneous mixture.”
Co-corresponding author William Shih, PhD, a core faculty member at the Wyss Institute and professor at HMS and the Dana-Farber Cancer Institute, further commented, “Single-molecule proteomics is still largely a pipe dream due to challenges in scaling and resolution. Our present work shows that force-based sequence fingerprinting has the potential to realize this dream. Our ultimate ambition is to efficiently read not just protein sequences, but also protein structures in a high-throughput manner.”
The scientists’ next step toward that goal is validating their calipers for low-force structural measurements on folded proteins and their complexes, investigating their potential use for structural biology and proteomics. “DNCs could potentially be used to measure distances between multiple residues of a protein in its folded structure, which would enable the characterization of the dynamic 3D structures of biomolecules and biomolecular complexes, complementing existing biophysical methods for structural elucidation,” they wrote.
The team is also working on increasing the technology’s throughput to further speed up the analysis of mixed samples. “DNC could also be integrated into other force spectroscopy approaches, to incorporate additional features or improve dynamic range, spatial precision or throughput,” they suggested. “DNC provides a powerful approach for characterizing distances and geometries within nanoscale complexes, with the potential to affect a wide range of fields, from proteomics and nanotechnology, to structural biology and drug discovery.”
“This research integrates molecular biophysics with cutting-edge DNA nanotechonlogy pioneered here at the Wyss Institute to allow us to interact with and analyze biological molecules in a truly novel way,” said Wyss founding director Don Ingber, MD, PhD, who is also the Judah Folkman professor of vascular biology at Harvard Medical School and BCH, and professor of bioengineering at the Harvard John A. Paulson School of Engineering and Applied Sciences. “When William and Wesley first posed this idea as a core challenge for the newly formed Molecular Robotics Initiative, it truly seemed like science fiction, but that is precisely the type of project we want to take on at the Wyss. I’m very proud of the team for making this technology a reality—it has the potential to totally change how we do science and develop therapeutics.”
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