Evidence map›Paper›PMID 42677391›Full record

ReviewChemical reviews2026

Membrane-Traversing Peptides: Mechanistic Landscapes, Assays, and Applications.

Adrian J Taveras, Erin A Kuang, Ryan P Ferrie, Ace Ellis, Alaina Tait, Rayhanus Salam, Kalina Hristova, William C Wimley

Abstract readReview
In one paragraph

Review in Chemical reviews, 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

8 authors.

Adrian J TaverasDepartment of Biochemistry and Molecular Biology, Tulane University School of Medicine, New Orleans, Louisiana70112, United States.ORCID 0009-0005-2485-4144
Erin A KuangDepartment of Microbiology and Immunology, Tulane University School of Medicine, New Orleans, Louisiana70112, United States.ORCID 0000-0002-7804-1000
Ryan P FerrieDepartment of Biochemistry and Molecular Biology, Tulane University School of Medicine, New Orleans, Louisiana70112, United States.
Ace EllisDepartment of Biochemistry and Molecular Biology, Tulane University School of Medicine, New Orleans, Louisiana70112, United States.ORCID 0009-0004-3948-0125
Alaina TaitDepartment of Biochemistry and Molecular Biology, Tulane University School of Medicine, New Orleans, Louisiana70112, United States.
Rayhanus SalamDepartment of Biochemistry and Molecular Biology, Tulane University School of Medicine, New Orleans, Louisiana70112, United States.ORCID 0000-0002-3007-6108
Kalina HristovaInstitute for NanoBioTechnology, Johns Hopkins University, Baltimore, Maryland21218, United States.ORCID 0000-0003-4274-4406
William C WimleyDepartment of Biochemistry and Molecular Biology, Tulane University School of Medicine, New Orleans, Louisiana70112, United States.ORCID 0000-0003-2967-5186

Funding

Division of Materials Research DMR-2534515Division of Materials Research DMR-2534516NIGMS NIH HHS 1R01151326
6 · The paper itself

Abstract

Lipid bilayer membranes are essential cellular permeability barriers that strictly limit the passage of polar molecules and macromolecules, thereby compartmentalizing cellular biochemistry and limiting the accessible chemical space for therapeutics. Membrane-traversing peptides (MTPs) are a diverse group of peptides defined by the ability to traverse synthetic or cellular membranes without causing permeabilization and without the assistance of specific transport proteins. These peptides fundamentally defy classical thermodynamic models of membrane permeability as they can cross lipid bilayers and deliver large polar cargoes, including peptides and proteins, into cells, despite having high net charge and low hydrophobicity. In this review, we challenge the idea of single, discrete mechanisms to describe how peptides traverse membranes and define a broad mechanistic landscape shaped by the conserved properties of MTPs and the unique physical chemistry and polymorphic phase behavior of lipid bilayers. We describe experimental assays and model systems that can be used to study MTP translocation and cargo delivery in synthetic systems and living cells. We use information obtained from comprehensive databases to consider the shared physical chemical space of MTPs. We also discuss key unanswered questions regarding mechanism, specificity, endosomal escape, and in vivo performance. Finally, we discuss illustrative examples and emerging translational applications of MTPs in intracellular drug delivery and molecular therapeutics. Together, these perspectives underscore the dual importance of MTPs as probes for fundamental biophysical studies of cell membranes and as promising tools to expand the universe of druggable intracellular targets.

Indexed as

Cell MembraneLipid BilayersPeptidesAnimalsCell Membrane PermeabilityHumansLipid BilayersPeptides

Identifiers

PMID42677391
PMCPMC13523643

What OpenQuestion holds

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Registered trials

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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.