Quantitative machine learning of protein interactions reveals the multiscale organization and molecular syntax of signaling networks. [Preprint]. 2026 September. doi: 10.64898/2026.09.25.754499.
Substrate-Derived Peptides for Selective Covalent Inhibition of Protein Tyrosine Kinases.
ACS Chem Biol.
2026 Aug 24;. doi: 10.1021/acschembio.6c00468. [Epub ahead of print] PubMed PMID:
42669292; PubMed Central PMCID:
PMC13590119.
In situ identification of substrates of the protein tyrosine phosphatase PTP1B using site-specific photo-crosslinking. bioRxiv [Preprint]. Version v1. 2026 July. Available from: https://doi.org/10.64898/2026.07.06.736850.
Identification of substrates of the protein tyrosine phosphatase PTP1B using <i>in situ</i> site-specific photo-crosslinking. [Preprint]. 2026 July. doi: 10.64898/2026.07.06.736850.
Multiplexed single-cell transcriptomics reveals diverse phenotypic outcomes for pathogenic SHP2 variants.
Sci Adv.
2026 May 22;12(21):eaea9389. doi: 10.1126/sciadv.aea9389. Epub 2026 May 22. PubMed PMID:
42172315; PubMed Central PMCID:
PMC13196782.
Substrate-derived peptides for selective covalent inhibition of protein tyrosine kinases.
bioRxiv.
2026 May 14;. doi: 10.64898/2026.05.11.724146. PubMed PMID:
42182222; PubMed Central PMCID:
PMC13192911.
A bis-phosphorylated peptide wrangles the SHP2 tandem SH2 domains into shape.
Structure.
2026 Mar 5;34(3):388-390. doi: 10.1016/j.str.2026.02.003. PubMed PMID:
41795456.
A Scalable Design for Proximity-Inducing Molecules.
bioRxiv.
2026 Feb 21;. doi: 10.64898/2026.02.20.706349. PubMed PMID:
41756985; PubMed Central PMCID:
PMC12934950.
Pervanadate: So much more than a protein tyrosine phosphatase inhibitor.
Sci Signal.
2026 Jan 20;19(921):eaed6832. doi: 10.1126/scisignal.aed6832. Epub 2026 Jan 20. PubMed PMID:
41557760.
Profiling tyrosine kinase substrate recognition using bacterial peptide display and deep sequencing.
bioRxiv.
2025 Dec 30;. doi: 10.64898/2025.12.28.696772. PubMed PMID:
41509325; PubMed Central PMCID:
PMC12776416.
Proximity-labeling proteomics reveals remodeled interactomes and altered localization of pathogenic SHP2 variants.
EMBO Rep.
2026 Feb;27(3):793-826. doi: 10.1038/s44319-025-00674-4. Epub 2025 Dec 22. PubMed PMID:
41429940; PubMed Central PMCID:
PMC12894930.
The pathogenic E139D mutation stabilizes a non-canonical active state of the multi-domain phosphatase SHP2.
Protein Sci.
2025 Dec;34(12):e70373. doi: 10.1002/pro.70373. PubMed PMID:
41225768; PubMed Central PMCID:
PMC12611872.
Accurate affinity models for SH2 domains from peptide binding assays and free-energy regression.
Protein Sci.
2025 Nov;34(11):e70317. doi: 10.1002/pro.70317. PubMed PMID:
41088778; PubMed Central PMCID:
PMC12521615.
The pathogenic E139D mutation stabilizes a non-canonical active state of the multi-domain phosphatase SHP2.
bioRxiv.
2025 Oct 1;. doi: 10.1101/2025.07.02.662799. PubMed PMID:
40631229; PubMed Central PMCID:
PMC12236607.
Proximity-labeling proteomics reveals remodeled interactomes and altered localization of pathogenic SHP2 variants.
bioRxiv.
2025 Sep 8;. doi: 10.1101/2025.02.26.640373. PubMed PMID:
40661614; PubMed Central PMCID:
PMC12258515.
Multiplexed single-cell transcriptomics reveals diverse phenotypic outcomes for pathogenic SHP2 variants.
bioRxiv.
2025 Jul 2;. doi: 10.1101/2025.06.30.662374. PubMed PMID:
40631144; PubMed Central PMCID:
PMC12236728.
Deep mutational scanning of the multi-domain phosphatase SHP2 reveals mechanisms of regulation and pathogenicity.
Nat Commun.
2025 Jul 1;16(1):5464. doi: 10.1038/s41467-025-60641-4. PubMed PMID:
40595497; PubMed Central PMCID:
PMC12216643.
Allosteric inhibition rescues hydrocephalus caused by catalytically inactive Shp2.
bioRxiv.
2025 Feb 1;. doi: 10.1101/2025.01.28.635289. PubMed PMID:
39974929; PubMed Central PMCID:
PMC11838390.
SEC-MX: an approach to systematically study the interplay between protein assembly states and phosphorylation.
Nat Commun.
2025 Jan 30;16(1):1176. doi: 10.1038/s41467-025-56303-0. PubMed PMID:
39885126; PubMed Central PMCID:
PMC11782603.
Accurate sequence-to-affinity models for SH2 domains from multi-round peptide binding assays coupled with free-energy regression.
bioRxiv.
2025 Jan 5;. doi: 10.1101/2024.12.23.630085. PubMed PMID:
39764007; PubMed Central PMCID:
PMC11703206.
Allosteric regulation of the tyrosine phosphatase PTP1B by a protein-protein interaction.
Protein Sci.
2025 Jan;34(1):e70016. doi: 10.1002/pro.70016. PubMed PMID:
39723820; PubMed Central PMCID:
PMC11670308.
A Multiplexed SEC-MS Approach to Systematically Study the Interplay Between Protein Assembly-States and Phosphorylation Events.
bioRxiv.
2024 Aug 1;. doi: 10.1101/2023.01.12.523793. PubMed PMID:
36711903; PubMed Central PMCID:
PMC9882152.
Crafting Unnatural Peptide Macrocycles via Rh(III)-Catalyzed Carboamidation.
Journal of the American Chemical Society. 2024 July; 146(30):20868-20877. doi: 10.1021/jacs.4c05248.
The pathogenic T42A mutation in SHP2 rewires the interaction specificity of its N-terminal regulatory domain.
Proc Natl Acad Sci U S A.
2024 Jul 23;121(30):e2407159121. doi: 10.1073/pnas.2407159121. Epub 2024 Jul 16. PubMed PMID:
39012820; PubMed Central PMCID:
PMC11287265.
Deep mutational scanning of a multi-domain signaling protein reveals mechanisms of regulation and pathogenicity. [Preprint]. 2024 May. doi: 10.1101/2024.05.13.593907.
The pathogenic T42A mutation in SHP2 rewires the interaction specificity of its N-terminal regulatory domain.
bioRxiv.
2024 Apr 9;. doi: 10.1101/2023.07.10.548257. PubMed PMID:
37502916; PubMed Central PMCID:
PMC10369915.
Photocatalytic Activation of Aryl(trifluoromethyl) Diazos to Carbenes for High-Resolution Protein Labeling with Red Light.
J Am Chem Soc.
2024 Jan 17;146(2):1337-1345. doi: 10.1021/jacs.3c09545. Epub 2024 Jan 2. PubMed PMID:
38165744; NIHMSID:NIHMS1971853.
TCR signaling promotes formation of an STS1-Cbl-b complex with pH-sensitive phosphatase activity that suppresses T cell function in acidic environments.
Immunity.
2023 Dec 12;56(12):2682-2698.e9. doi: 10.1016/j.immuni.2023.11.010. PubMed PMID:
38091950; PubMed Central PMCID:
PMC10785950.
Mapping the Chemical Space of Active-Site Targeted Covalent Ligands for Protein Tyrosine Phosphatases.
Chembiochem.
2023 May 16;24(10):e202200706. doi: 10.1002/cbic.202200706. Epub 2023 Apr 26. PubMed PMID:
36893077; PubMed Central PMCID:
PMC10192133.
High-throughput profiling of sequence recognition by tyrosine kinases and SH2 domains using bacterial peptide display.
Elife.
2023 Mar 16;12. doi: 10.7554/eLife.82345. PubMed PMID:
36927728; PubMed Central PMCID:
PMC10065799.
High-throughput profiling of sequence recognition by tyrosine kinases and SH2 domains using bacterial peptide display.
eLife. 2023 March; 12:-. doi: 10.7554/eLife.82345.
Modular Synthesis of Unnatural Peptides via Rh(III)-Catalyzed Diastereoselective Three-Component Carboamidation Reaction.
Journal of the American Chemical Society. 2022 December; 145(2):1129-1135. doi: 10.1021/jacs.2c10793.
Saturation mutagenesis of a predicted ancestral Syk-family kinase.
Protein Sci.
2022 Oct;31(10):e4411. doi: 10.1002/pro.4411. PubMed PMID:
36173161; PubMed Central PMCID:
PMC9601881.
Prediction of protein-ligand binding affinity from sequencing data with interpretable machine learning.
Nat Biotechnol.
2022 Oct;40(10):1520-1527. doi: 10.1038/s41587-022-01307-0. Epub 2022 May 23. PubMed PMID:
35606422; PubMed Central PMCID:
PMC9546773.
A saturation-mutagenesis analysis of the interplay between stability and activation in Ras.
eLife. 2022 March; 11:-. doi: 10.7554/eLife.76595.
A Saturation-Mutagenesis Analysis of the Interplay Between Stability and Activation in Ras. [Preprint]. 2022 January. doi: 10.1101/2022.01.06.475190.
Differences in the dynamics of the <scp>tandem‐SH2</scp> modules of the Syk and <scp>ZAP</scp> ‐70 tyrosine kinases.
Protein Science. 2021 October; 30(12):2373-2384. doi: 10.1002/pro.4199.
Differences in the dynamics of the tandem-SH2 modules of the Syk and ZAP-70 tyrosine kinases. [Preprint]. 2021 July. doi: 10.1101/2021.07.20.453126.
Probing molecular specificity with deep sequencing and biophysically interpretable machine learning. [Preprint]. 2021 July. doi: 10.1101/2021.06.30.450414.
Identification, Characterization, and Optimization of Split Inteins.
Methods Mol Biol.
2020;2133:31-54. doi: 10.1007/978-1-0716-0434-2_3. PubMed PMID:
32144662.
Identification, Characterization, and Optimization of Split Inteins.
In:
Methods in Molecular Biology
[Internet]
New York, NY: Springer US; 2020. Chapter Chapter 3; 31-54p.
Available from: http://link.springer.com/10.1007/978-1-0716-0434-2_3.
Slow phosphorylation of a tyrosine residue in LAT optimizes T cell ligand discrimination.
Nat Immunol.
2019 Nov;20(11):1481-1493. doi: 10.1038/s41590-019-0502-2. Epub 2019 Oct 14. PubMed PMID:
31611699; PubMed Central PMCID:
PMC6858552.
Learning from ancestors.
Elife.
2019 Aug 13;8. doi: 10.7554/eLife.49976. PubMed PMID:
31407665; PubMed Central PMCID:
PMC6692129.
Variation in assembly stoichiometry in non‐metazoan homologs of the hub domain of Ca <sup>2+</sup> /calmodulin‐dependent protein kinase II.
Protein Science. 2019 April; 28(6):1071-1082. doi: 10.1002/pro.3614.
Variation in assembly stoichiometry in non-metazoan homologs of the hub domain of Ca2+/Calmodulin-dependent protein kinase II. [Preprint]. 2019 January. doi: 10.1101/536094.
Understanding molecular mechanisms in cell signaling through natural and artificial sequence variation.
Nat Struct Mol Biol.
2019 Jan;26(1):25-34. doi: 10.1038/s41594-018-0175-9. Epub 2018 Dec 31. Review. PubMed PMID:
30598552; PubMed Central PMCID:
PMC6463301.
The Src module: an ancient scaffold in the evolution of cytoplasmic tyrosine kinases.
Crit Rev Biochem Mol Biol.
2018 Oct;53(5):535-563. doi: 10.1080/10409238.2018.1495173. Epub 2018 Sep 5. Review. PubMed PMID:
30183386; PubMed Central PMCID:
PMC6328253.
Deep mutational analysis reveals functional trade-offs in the sequences of EGFR autophosphorylation sites.
Proc Natl Acad Sci U S A.
2018 Jul 31;115(31):E7303-E7312. doi: 10.1073/pnas.1803598115. Epub 2018 Jul 16. PubMed PMID:
30012625; PubMed Central PMCID:
PMC6077704.
Lck promotes Zap70-dependent LAT phosphorylation by bridging Zap70 to LAT.
Nat Immunol.
2018 Jul;19(7):733-741. doi: 10.1038/s41590-018-0131-1. Epub 2018 Jun 18. PubMed PMID:
29915297; PubMed Central PMCID:
PMC6202249.
ZAP-70 in Signaling, Biology, and Disease.
Annual Review of Immunology. 2018 April; 36(1):127-156. doi: 10.1146/annurev-immunol-042617-053335.
What would you like to do?