Evidence map›Paper›PMID 30373828›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2018

The in silico human surfaceome.

Damaris Bausch-Fluck, Ulrich Goldmann, Sebastian Müller, Marc van Oostrum, Maik Müller, Olga T Schubert, Bernd Wollscheid

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 238 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
238citing papers in PubMed, 1 pooled it
15.6field-weighted citation impact, top 1% of its field
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

238 citing papers in PubMed, 1 synthesis or guideline pooled it, 407 citations in OpenAlex.

  1. Pooled it
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  9. A Framework for Benchmarking Pathway Reconstruction Algorithms.bioRxiv : the preprint server for biology · 2026
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178 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

7 authors at 1 institution in 1 country.

Damaris Bausch-FluckInstitute of Molecular Systems Biology at the Department of Biology, ETH Zurich, 8093 Zurich, Switzerland.ORCID 0000-0002-7593-2262
Ulrich GoldmannInstitute of Molecular Systems Biology at the Department of Biology, ETH Zurich, 8093 Zurich, Switzerland.
Sebastian MüllerInstitute of Molecular Systems Biology at the Department of Biology, ETH Zurich, 8093 Zurich, Switzerland.
Marc van OostrumInstitute of Molecular Systems Biology at the Department of Biology, ETH Zurich, 8093 Zurich, Switzerland.
Maik MüllerInstitute of Molecular Systems Biology at the Department of Biology, ETH Zurich, 8093 Zurich, Switzerland.
Olga T SchubertInstitute of Molecular Systems Biology at the Department of Biology, ETH Zurich, 8093 Zurich, Switzerland.ORCID 0000-0002-2613-0714
Bernd WollscheidInstitute of Molecular Systems Biology at the Department of Biology, ETH Zurich, 8093 Zurich, Switzerland; wbernd@ethz.ch.ORCID 0000-0002-3923-1610
ETH Zurich · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cell-surface proteins are of great biomedical importance, as demonstrated by the fact that 66% of approved human drugs listed in the DrugBank database target a cell-surface protein. Despite this biomedical relevance, there has been no comprehensive assessment of the human surfaceome, and only a fraction of the predicted 5,000 human transmembrane proteins have been shown to be located at the plasma membrane. To enable analysis of the human surfaceome, we developed the surfaceome predictor SURFY, based on machine learning. As a training set, we used experimentally verified high-confidence cell-surface proteins from the Cell Surface Protein Atlas (CSPA) and trained a random forest classifier on 131 features per protein and, specifically, per topological domain. SURFY was used to predict a human surfaceome of 2,886 proteins with an accuracy of 93.5%, which shows excellent overlap with known cell-surface protein classes (i.e., receptors). In deposited mRNA data, we found that between 543 and 1,100 surfaceome genes were expressed in cancer cell lines and maximally 1,700 surfaceome genes were expressed in embryonic stem cells and derivative lines. Thus, the surfaceome diversity depends on cell type and appears to be more dynamic than the nonsurface proteome. To make the predicted surfaceome readily accessible to the research community, we provide visualization tools for intuitive interrogation (wlab.ethz.ch/surfaceome). The in silico surfaceome enables the filtering of data generated by multiomics screens and supports the elucidation of the surfaceome nanoscale organization.

Indexed as

Cell MembraneComputer SimulationDatabases, ChemicalForecastingHumansMachine LearningMembrane ProteinsProteomeProteomicsMembrane ProteinsProteomecell surface proteinmachine learningmultiomicssurfaceomeSURFY

Identifiers

PMID30373828
PMCPMC6243280
OpenAlexW2898873576

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.