Evidence map›Paper›PMID 42341757›Full record

ArticleCell reports methods2026

Rapid discovery of cell-surface glycosylation regulators using a lectin-based magnetic CRISPR screen.

Jimmy Kim, Halen Kovacs, Simon Wisnovsky

Abstract read
In one paragraph

Article in Cell reports methods, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

3 authors.

Jimmy KimUniversity of British Columbia, Faculty of Pharmaceutical Sciences, Vancouver, BC, Canada.
Halen KovacsUniversity of British Columbia, Faculty of Pharmaceutical Sciences, Vancouver, BC, Canada.
Simon WisnovskyUniversity of British Columbia, Faculty of Pharmaceutical Sciences, Vancouver, BC, Canada. Electronic address: simon.wisnovsky@ubc.ca.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

FACS-based CRISPR screening has emerged as a potent tool for dissecting the genetic networks that regulate cell-surface glycosylation. However, existing protocols can be tedious and are not compatible with many cell models. We developed a lectin-based magnetic-activated cell sorting platform (Lec-MACS) that enables rapid identification of genes controlling expression of specific cell-surface glycans. Lec-MACS offers superior speed and multiplexability compared to FACS, while also being well-suited to studying cell models that are not amenable to flow-based sorting. We subsequently applied Lec-MACS to map genes that regulate hypersialylation in an adherent breast cancer cell line. Subsequent hit validation confirmed an unexpected link between DNA damage response signaling and cell-surface sialylation. The Lec-MACS method will expand the scope and throughput of genetic screens targeted at cell-surface glycans.

Indexed as

Cell MembraneClustered Regularly Interspaced Short Palindromic RepeatsCRISPR-Cas SystemsLectinsCell Line, TumorFlow CytometryGlycosylationHumansPolysaccharidesLectinsPolysaccharidesCP: biotechnologyCRISPR screeningglycanslectinsmagnetic cell sortingsialic acidtumor immunology

Identifiers

PMID42341757
PMCPMC13494540

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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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.