Evidence map›Paper›PMID 35606422›Full record

ArticleNature biotechnology2022

Prediction of protein-ligand binding affinity from sequencing data with interpretable machine learning.

H Tomas Rube, Chaitanya Rastogi, Siqian Feng, Judith F Kribelbauer, Allyson Li, Basheer Becerra, Lucas A N Melo, Bach Viet Do, Xiaoting Li, Hammaad H Adam and 3 more

Abstract read
In one paragraph

Article in Nature biotechnology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 67 papers.

0numbers the graph read from it
0cells of the map it votes in
67citing 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

67 citing papers in PubMed.

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  20. aBIOTECH · 2025
    Review

7 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors.

H Tomas RubeDepartment of Bioengineering, University of California, Merced, Merced, CA, USA.
Chaitanya RastogiDepartment of Biological Sciences, Columbia University, New York, NY, USA.ORCID 0000-0001-9155-9341
Siqian Feng *Department of Biochemistry and Molecular Biophysics, Columbia University, New York, NY, USA.ORCID 0000-0003-0650-9134
Judith F Kribelbauer *Department of Biological Sciences, Columbia University, New York, NY, USA.ORCID 0000-0002-8072-7773
Allyson Li *Department of Chemistry, Columbia University, New York, NY, USA.ORCID 0000-0003-2359-7703
Basheer BecerraDepartment of Biological Sciences, Columbia University, New York, NY, USA.ORCID 0000-0003-4403-7959
Lucas A N MeloDepartment of Biological Sciences, Columbia University, New York, NY, USA.ORCID 0000-0002-7563-7554
Bach Viet DoDepartment of Biological Sciences, Columbia University, New York, NY, USA.
Xiaoting LiDepartment of Biological Sciences, Columbia University, New York, NY, USA.
Hammaad H AdamDepartment of Biological Sciences, Columbia University, New York, NY, USA.
Neel H ShahDepartment of Chemistry, Columbia University, New York, NY, USA.ORCID 0000-0002-1186-0626
Richard S MannDepartment of Biochemistry and Molecular Biophysics, Columbia University, New York, NY, USA.ORCID 0000-0002-4749-2765
Harmen J BussemakerDepartment of Biological Sciences, Columbia University, New York, NY, USA. hjb2004@columbia.edu.ORCID 0000-0002-7274-5277

Funding

Training Program in Bioinformatics and Integrative GenomicsT32HG002295 · NHGRI · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI Peter J Park · 2001 to 2026
$15.8M
Inferring regulatory circuitry from microarray dataR01HG003008 · NHGRI · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI BUSSEMAKER, HARMEN J · 2004 to 2020
$7.0M
Interpreting and Deploying Genomic Information During Animal DevelopmentR35GM118336 · NIGMS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI RICHARD S MANN · 2016 to 2026
$6.9M
Statistical models for fine-mapping and interpretation of schizophrenia-associated lociR01MH106842 · NIMH · NEW YORK GENOME CENTER · PI BUSSEMAKER, HARMEN J, LAPPALAINEN, TUULI · 2015 to 2024
$5.0M
NHGRI NIH HHS R01 HG003008NHGRI NIH HHS T32 HG002295NIGMS NIH HHS R35 GM118336NIMH NIH HHS R01 MH106842
6 · The paper itself

Abstract

Protein-ligand interactions are increasingly profiled at high throughput using affinity selection and massively parallel sequencing. However, these assays do not provide the biophysical parameters that most rigorously quantify molecular interactions. Here we describe a flexible machine learning method, called ProBound, that accurately defines sequence recognition in terms of equilibrium binding constants or kinetic rates. This is achieved using a multi-layered maximum-likelihood framework that models both the molecular interactions and the data generation process. We show that ProBound quantifies transcription factor (TF) behavior with models that predict binding affinity over a range exceeding that of previous resources; captures the impact of DNA modifications and conformational flexibility of multi-TF complexes; and infers specificity directly from in vivo data such as ChIP-seq without peak calling. When coupled with an assay called K

Indexed as

Machine LearningTranscription FactorsBinding SitesChromatin ImmunoprecipitationDNALigandsProtein BindingDNALigandsTranscription Factors

Identifiers

PMID35606422
PMCPMC9546773

What OpenQuestion 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 OpenQuestion graph.