Hydrogen‐Deuterium Exchange Mass Spectrometry for Molecular Glue Characterization
Source abstract
Abstract
Abstract Molecular glues are powerful bioactive molecules that stabilize protein–protein interactions. Yet, the precise mechanisms by which many molecular glues exert their adhesive effects are still not well understood. Native mass spectrometry is an established technique used to monitor the stoichiometry and binding equilibria of molecular glue‐induced protein–protein interactions. However, knowledge is lacking on how protein interaction dynamics change upon molecular glue‐induced stabilization, and what conformational changes occur that enhance the stability of the resulting protein‐protein‐glue ternary complex. Here, hydrogen‐deuterium exchange mass spectrometry (HDX‐MS) is showcased as an analytical tool for molecular glue characterization. Using a broadly applicable molecular glue system involving the eukaryotic regulatory protein 14‐3‐3, its binding partners, and the molecular glue fusicoccin A, the power of HDX‐MS is shown in revealing not only molecular glue binding sites, but also conformational changes upon glue binding that result in differentially stabilized protein‐protein complexes. Overall, the HDX‐MS approach will become highly envisaged and valuable for the characterization of molecular glues, guiding their optimization toward successful design.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: 14-3-3 protein interactions · Ubiquitin and proteasome pathways · Peptidase Inhibition and Analysis
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
School of Biosciences University of Birmingham Birmingham B15 2TT UK
Institute of Structural and Chemical Biology and School of Chemistry University of Leicester Leicester LE1 7RH UK
Funding
Engineering and Physical Sciences Research Council · Medical Research Foundation · Biotechnology and Biological Sciences Research Council
References (62)
Show source-provided references
1. Safari‐Alighiarloo N. · Gastroenterol Hepatol. Bed. Bench · 2014 · 7 · 17
2. 10.1038/s41587‐024‐02428‐410.1038/s41587‐024‐02428‐4 ↗
3. 10.1016/j.cell.2024.10.03810.1016/j.cell.2024.10.038 ↗
4. 10.1038/s41392-024-02036-310.1038/s41392-024-02036-3 ↗
5. 10.1016/j.cbpa.2022.10216910.1016/j.cbpa.2022.102169 ↗
6. 10.1016/j.chembiol.2024.04.00210.1016/j.chembiol.2024.04.002 ↗
7. 10.1016/j.slasd.2023.12.00810.1016/j.slasd.2023.12.008 ↗
8. 10.1016/j.sbi.2025.10300710.1016/j.sbi.2025.103007 ↗
9. 10.1146/annurev-pharmtox-022123-10414710.1146/annurev-pharmtox-022123-104147 ↗
10. 10.1038/s41586-020-2760-410.1038/s41586-020-2760-4 ↗
11. 10.1016/0092-8674(91)90124-H10.1016/0092-8674(91)90124-H ↗
12. 10.1038/s41589-020-0557-210.1038/s41589-020-0557-2 ↗
13. 10.1080/17460441.2017.134660810.1080/17460441.2017.1346608 ↗
14. 10.1126/science.117731910.1126/science.1177319 ↗
15. 10.1016/0024-3205(95)02233-310.1016/0024-3205(95)02233-3 ↗
16. 10.1016/j.celrep.2017.08.08110.1016/j.celrep.2017.08.081 ↗
17. 10.1039/D1MD00172H10.1039/D1MD00172H ↗
18. 10.7554/eLife.5999410.7554/eLife.59994 ↗
19. 10.1021/jacs.3c0830710.1021/jacs.3c08307 ↗
20. 10.1021/acscentsci.2c0144910.1021/acscentsci.2c01449 ↗
21. 10.1016/j.slasd.2024.10016510.1016/j.slasd.2024.100165 ↗
22. 10.1038/s41467-021-27818-z10.1038/s41467-021-27818-z ↗
23. 10.1016/j.jbc.2024.10565110.1016/j.jbc.2024.105651 ↗
24. 10.1039/D1SC01450A10.1039/D1SC01450A ↗
25. 10.1039/D4AN00110A10.1039/D4AN00110A ↗
26. 10.1021/jacs.3c0265510.1021/jacs.3c02655 ↗
27. 10.1021/jasms.4c0042910.1021/jasms.4c00429 ↗
28. 10.1039/D3SC01732J10.1039/D3SC01732J ↗
29. 10.1016/j.chembiol.2021.05.00510.1016/j.chembiol.2021.05.005 ↗
30. 10.1016/j.mcpro.2024.10085310.1016/j.mcpro.2024.100853 ↗
31. 10.1021/acs.analchem.0c0428110.1021/acs.analchem.0c04281 ↗
32. 10.1021/bi200377c10.1021/bi200377c ↗
33. 10.1021/acs.analchem.7b0112110.1021/acs.analchem.7b01121 ↗
34. 10.1073/pnas.180366211510.1073/pnas.1803662115 ↗
35. 10.1021/acschembio.1c0037610.1021/acschembio.1c00376 ↗
36. 10.1126/science.add757410.1126/science.add7574 ↗
37. 10.1038/s41467-022-33638-610.1038/s41467-022-33638-6 ↗
38. 10.1038/s41388-018-0348-310.1038/s41388-018-0348-3 ↗
39. 10.1016/j.molcel.2023.02.01810.1016/j.molcel.2023.02.018 ↗
40. 10.1021/acs.jmedchem.7b0057410.1021/acs.jmedchem.7b00574 ↗
41. 10.1002/cbic.20240021410.1002/cbic.202400214 ↗
42. 10.1016/j.sbi.2024.10282210.1016/j.sbi.2024.102822 ↗
43. 10.1093/emboj/cdg10410.1093/emboj/cdg104 ↗
44. 10.1002/iub.123910.1002/iub.1239 ↗
45. 10.1073/pnas.122080911010.1073/pnas.1220809110 ↗
46. 10.1016/j.jbc.2023.10485510.1016/j.jbc.2023.104855 ↗
47. Visser E. J. · bioRxiv · 2024
48. 10.1042/BCJ2016107810.1042/BCJ20161078 ↗
49. 10.1111/febs.1521510.1111/febs.15215 ↗
50. 10.1074/jbc.M113.54455110.1074/jbc.M113.544551 ↗
51. 10.1073/pnas.060577910310.1073/pnas.0605779103 ↗
52. 10.1038/srep4611410.1038/srep46114 ↗
53. 10.1371/journal.pone.018063310.1371/journal.pone.0180633 ↗
54. 10.3390/ijms1502279410.3390/ijms15022794 ↗
55. 10.1038/s41467-021-21908-810.1038/s41467-021-21908-8 ↗
56. 10.1016/j.jmb.2022.16747910.1016/j.jmb.2022.167479 ↗
57. 10.1074/jbc.M30693920010.1074/jbc.M306939200 ↗
58. 10.1002/prot.1021010.1002/prot.10210 ↗
59. 10.1021/acs.chemrev.1c0022210.1021/acs.chemrev.1c00222 ↗
60. 10.1021/acs.analchem.2c0318310.1021/acs.analchem.2c03183 ↗
61. 10.1021/jasms.1c0037510.1021/jasms.1c00375 ↗
62. 10.1371/journal.pone.004209010.1371/journal.pone.0042090 ↗