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Real-time dynamic single-molecule protein sequencing on an integrated semiconductor device
Open accessPreprint — published as 10.1126/science.abo7651
Abstract
Summary: Proteins are the main structural and functional components of cells, and their dynamic regulation and post-translational modifications (PTMs) underlie cellular phenotypes. Next-generation DNA sequencing technologies have revolutionized our understanding of heredity and gene regulation, but the complex and dynamic states of cells are not fully captured by the genome and transcriptome. Sensitive measurements of the proteome are needed to fully understand biological processes and changes to the proteome that occur in disease states. Studies of the proteome would benefit greatly from methods to directly sequence and digitally quantify proteins and detect PTMs with single-molecule sensitivity and precision. However current methods for studying the proteome lag behind DNA sequencing in throughput, sensitivity, and accessibility due to the complexity and dynamic range of the proteome, the chemical properties of proteins, and the inability to amplify proteins. Here, we demonstrate single-molecule protein sequencing on a compact benchtop instrument using a dynamic sequencing by stepwise degradation approach in which single surface-immobilized peptide molecules are probed in real-time by a mixture of dye-labeled N-terminal amino acid recognizers and simultaneously cleaved by aminopeptidases. By measuring fluorescence intensity, lifetime, and binding kinetics of recognizers on an integrated semiconductor chip we are able to annotate amino acids and identify the peptide sequence. We describe the expansion of the number of recognizable amino acids and demonstrate the kinetic principles that allow individual recognizers to identify multiple amino acids in a highly information-rich manner that is sensitive to adjacent residues. Furthermore, we demonstrate that our method is compatible with both synthetic and natural peptides, and capable of detecting single amino acid changes and PTMs. We anticipate that with further development our protein sequencing method will offer a sensitive, scalable, and accessible platform for studies of the proteome.
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How many human proteoforms are there?
Aebersold, R., Agar, J. N., Amster, I. J., Baker, M. S., Bertozzi, C. R., Boja, E. S., Costello, C. E., Cravatt, B. F., Fenselau, C., Garcia, B. A., et al. (2018) · Nature Chemical Biology · doi:10.1038/nchembio.2576 · Cited by 907
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Research works printed but not linked: 23
- 10.1038/nrg.2016.49 · DOI · Paper page
- 10.1126/sciadv.aax8978 · DOI
- 10.1038/msb.2011.82 · DOI · Paper page
- 10.1074/mcp.R200007-MCP200 · DOI · Paper page
- 10.1016/j.cell.2016.03.014 · DOI · Paper page
- 2019, Engineering ClpS for selective and enhanced N-terminal amino acid binding, Appl. Microbiol. Biotechnol, 103, 2621, 10.1007/s00253-019-09624-2 · DOI
- 10.1016/S1097-2765(02)00485-9 · DOI
- 10.1016/j.str.2015.12.008 · DOI
- 10.1016/j.tibs.2007.08.010 · DOI
- 10.1111/j.1365-2958.2009.06600.x · DOI
- 10.1021/bi047736j · DOI
- 10.1038/nsmb.1907 · DOI
- 10.1016/j.str.2017.03.004 · DOI
- 10.1038/nbt.4278 · DOI
- 10.1101/2021.10.11.463967 · DOI
- 2021, Bottom-up fabrication of a proteasome-nanopore that unravels and processes single proteins, Nat. Chem, 13, 1192, 10.1038/s41557-021-00824-w · DOI
- 10.1126/science.abl4381 · DOI
- 2021, The emerging landscape of single-molecule protein sequencing technologies, Nat. Methods, 18, 604, 10.1038/s41592-021-01143-1 · DOI
- 2015, A theoretical justification for single molecule peptide sequencing, PLoS Comput. Biol, 11, e1004080, 10.1371/journal.pcbi.1004080 · DOI
- 2015, Empirical estimation of local dielectric constants: Toward atomistic design of collagen mimetic peptides, Biopolymers, 104, 360, 10.1002/bip.22644 · DOI
- 2019, Generalized born implicit solvent models for biomolecules, Annu. Rev. Biophys, 48, 275, 10.1146/annurev-biophys-052118-115325 · DOI
- 2020, ff19SB: Amino-Acid-Specific Protein Backbone Parameters Trained against Quantum Mechanics Energy Surfaces in Solution, J. Chem. Theory Comput, 16, 528, 10.1021/acs.jctc.9b00591 · DOI
- 10.1021/ct300418h · DOI
Metadata
- Authors
- Reed, B. D., Meyer, M. J., Abramzon, V., Ad, O., Adcock, P., Ahmad, F. R., Alppay, G., Ball, J. A., Beach, J., Belhachemi, D., Bellofiore, A., Bellos, M., Beltrán, J. F., Betts, A., Bhuiya, M. W., Blacklock, K., Boer, R., Boisvert, D., Brault, N. D., Buxbaum, A., Caprio, S., Choi, C., Christian, T. D., Clancy, R., Clark, J., Connolly, T., Croce, K. F., Cullen, R., Davey, M., Davidson, J., Elshenawy, M. M., Ferrigno, M., Frier, D., Gudipati, S., Hamill, S., He, Z., Hosali, S., Huang, H., Huang, L., Kabiri, A., Kriger, G., Lathrop, B., Li, A., Lim, P., Liu, S., Luo, F., Lv, C., Ma, X., McCormack, E., Millham, M., Nani, R., Pandey, M., Parillo, J., Patel, G., Pike, D. H., Preston, K., Pichard-Kostuch, A., Rearick, K., Rearick, T., Ribezzi-Crivellari, M., Schmid, G., Schultz, J., Shi, X., Singh, B., Srivastava, N., Stewman, S. F., Thurston, T. R., Trioli, P., Tullman, J., Wang, X., Wang, Y.-C., Webster, E. A. G., Zhang, Z., Zuniga, J., Patel, S. S., Griffiths, A. D., van Oijen, A. M., McKenna, M., Dyer, M. D., & Rothberg, J. M.
- Affiliations
- Centre National de la Recherche Scientifique (FR)
- Rutgers, The State University of New Jersey (US)
- University of Wollongong (AU)
- Corresponding author
- Reed, Brian D.
- ORCID
- Reed, Brian D.
- Meyer, Michael J.
- Ahmad, Faisal R.
- Ball, James A.
- Belhachemi, Dominique
- Bellofiore, Anthony
- Beltrán, Juan Felipe
- Bhuiya, Mohammad Wadud
- Blacklock, Kristin
- Boer, Robert
- Boisvert, David
- Brault, Norman D.
- Buxbaum, Aaron
- Christian, Thomas D.
- Connolly, Thomas
- Croce, Kathren Fink
- Davey, Mel
- Davidson, Jack
- Elshenawy, Mohamed M.
- Frier, Daniel
- Gudipati, Saketh
- Hamill, Stephanie
- He, Zhaoyu
- Hosali, Sharath
- Huang, Haidong
- Huang, Le
- Kabiri, Ali
- Li, An
- Lim, Peter
- Liu, Stephen
- Lv, Caixia
- Ma, Xiaoxiao
- McCormack, Evan
- Pandey, Manjula
- Patel, Gayatri
- Pike, Douglas H.
- Preston, Kyle
- Pichard-Kostuch, Adeline
- Rearick, Kyle
- Shi, Xinghua
- Srivastava, Nikita
- Stewman, Shannon F.
- Trioli, Philip
- Tullman, Jennifer
- Zhang, Zhizhuo
- Patel, Smita S.
- Griffiths, Andrew D.
- van Oijen, Antoine M.
- Dyer, Matthew D.
- Venue
- Science
- Publisher
- openRxiv
- Published
- 2022-01-05
- Volume
- 378
- Issue
- 6616
- Pages
- 186-192
- ISSN
- 0036-8075 (ISSN-L)
- OpenAlex
- W4305040598
- Cited by
- 134
- References
- 1
- Citations by year
- 2026: 28 · 2025: 34 · 2024: 33 · 2023: 27 · 2022: 11
- FWCI
- 11.67
- Type
- journal article
- Language
- en
- Open access
- green
- doi.org
- Locations
- Science (publishedVersion)
- bioRxiv (Cold Spring Harbor Laboratory) (acceptedVersion)
- PubMed (publishedVersion)
- Research Online (University of Wollongong) (submittedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Biophysics › Advanced Fluorescence Microscopy Techniques
- Physical Sciences › Engineering › Biomedical Engineering › Microfluidic and Capillary Electrophoresis Applications
- Physical Sciences › Chemistry › Spectroscopy › Advanced Proteomics Techniques and Applications
- Keywords
- single-molecule protein sequencing, fluorescence lifetime, binding kinetics, post-translational modification
- MeSH terms
- Amino Acids, Aminopeptidases, Peptides, Semiconductors, Sequence Analysis, Protein, Proteome, Proteomics
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