Evidence map›Paper›PMID 40720654›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2025

Combining MicroED and native mass spectrometry for structural discovery of enzyme-small molecule complexes.

Niko W Vlahakis, Cameron W Flowers, Mengting Liu, Matthew P Agdanowski, Samuel Johnson, Jacob A Summers, Lian M C Jacobs, Catherine Keyser, Phoebe Russell, Samuel L Rose and 12 more

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

22 authors.

Niko W VlahakisDepartment of Chemistry and Biochemistry, University of California, Los Angeles, CA 90095.ORCID 0000-0002-5092-0265
Cameron W FlowersDepartment of Chemistry and Biochemistry, University of California, Los Angeles, CA 90095.ORCID 0009-0005-2613-1150
Mengting LiuDepartment of Chemical and Biomolecular Engineering, University of California Los Angeles, Los Angeles, CA 90095.
Matthew P AgdanowskiDepartment of Chemistry and Biochemistry, University of California, Los Angeles, CA 90095.ORCID 0000-0001-7796-4287
Samuel JohnsonDivision of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, CA 91125.
Jacob A SummersDepartment of Structural Biology, Stanford University School of Medicine, Stanford, CA 94304.
Lian M C JacobsDepartment of Molecular Medicine, Morsani College of Medicine, University of South Florida, Tampa, FL 33612.ORCID 0000-0002-9939-653X
Catherine KeyserDepartment of Chemistry and Biochemistry, University of California, Los Angeles, CA 90095.
Phoebe RussellDepartment of Chemistry and Biochemistry, University of California, Los Angeles, CA 90095.
Samuel L RoseEuropean Synchrotron Radiation Facility-The European Synchrotron, Grenoble 38000, France.ORCID 0000-0003-4824-4066
Julien OrlansEuropean Synchrotron Radiation Facility-The European Synchrotron, Grenoble 38000, France.
Nima AdhamiDepartment of Chemistry and Biochemistry, University of California, Los Angeles, CA 90095.
Yu ChenDepartment of Chemistry and Biochemistry, University of California, Los Angeles, CA 90095.ORCID 0009-0001-2693-1693
Michael R SawayaDepartment of Chemistry and Biochemistry, University of California, Los Angeles, CA 90095.ORCID 0000-0003-0874-9043
Shibom BasuEuropean Molecular Biology Laboratory, Grenoble 38000, France.
Daniele de SanctisEuropean Synchrotron Radiation Facility-The European Synchrotron, Grenoble 38000, France.ORCID 0000-0003-0391-8290
Yu ChenDepartment of Molecular Medicine, Morsani College of Medicine, University of South Florida, Tampa, FL 33612.
Soichi WakatsukiDepartment of Structural Biology, Stanford University School of Medicine, Stanford, CA 94304.
Hosea M NelsonDivision of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, CA 91125.
Joseph A LooDepartment of Chemistry and Biochemistry, University of California, Los Angeles, CA 90095.ORCID 0000-0001-9989-1437
Yi TangDepartment of Chemical and Biomolecular Engineering, University of California Los Angeles, Los Angeles, CA 90095.
Jose A RodriguezDepartment of Chemistry and Biochemistry, University of California, Los Angeles, CA 90095.ORCID 0000-0001-8471-2504

Funding

UCLA NIGMS T32 Program AssessmentT32GM007185 · NIGMS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI TORRES, JORGE · 1985 to 2020
$21.7M
Research Training in Cell and Molecular BiologyT32GM145388 · NIGMS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI Jorge Torres · 2022 to 2026
$5.2M
Micro Electron Diffraction of Toxic and/or Infectious Macromolecular NanoassembliesR35GM128867 · NIGMS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI Jose Alfonso Rodriguez · 2018 to 2026
$3.1M
Advancing Mass Spectrometry Analyses of Proteins, Assemblies, and ProteoformsR35GM145286 · NIGMS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI Joseph A Loo · 2022 to 2026
$1.9M
HHMI (HHMI) EPIHHS | NIH (NIH) GM128867HHS | NIH (NIH) GM145286NIGMS NIH HHS R35 GM128867NIGMS NIH HHS R35 GM145286NIGMS NIH HHS T32 GM007185NIGMS NIH HHS T32 GM145388
6 · The paper itself

Abstract

With the goal of accelerating the discovery of small molecule-protein complexes, we leverage fast, low-dose, event-based electron counting microcrystal electron diffraction (MicroED) data collection and native mass spectrometry. This approach, which we term electron diffraction with native mass spectrometry (ED-MS), allows assignment of protein target structures bound to ligands with data obtained from crystal slurries soaked with mixtures of known inhibitors and crude biosynthetic reactions. This extends to libraries of printed ligands dispensed directly onto TEM grids for later soaking with microcrystal slurries, and complexes with noncovalent ligands. ED-MS resolves structures of the natural product, epoxide-based cysteine protease inhibitor E-64, and its biosynthetic analogs bound to the model cysteine protease, papain. It further identifies papain binding to its preferred natural products, by showing that two analogs of E-64 outcompete others in binding to papain crystals, and by detecting papain bound to E-64 and an analog from crude biosynthetic reactions, without purification. ED-MS also resolves binding of the CTX-M-14 β-lactamase, a target of active drug development, to the non-β-lactam inhibitor, avibactam, alone or in a cocktail of unrelated compounds. These results illustrate the utility of ED-MS for natural product ligand discovery and for structure-based screening of small molecule binders to macromolecular targets, promising utility for drug discovery.

Indexed as

Mass SpectrometryPapainSmall Molecule LibrariesCysteine Proteinase InhibitorsDrug DiscoveryLigandsProtein BindingCysteine Proteinase InhibitorsLigandsPapainSmall Molecule LibrariescryoEMenzymeligandmass spectrometryMicroED

Identifiers

PMID40720654
PMCPMC12337315

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.