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Cited by 339

The DOI matches its Crossref record; 142 of the 142 references it cites were found in a registry or an index.

Drugging Membrane Protein Interactions

Open access
Yin, Hang, Flynn, Aaron D.·2016·Annual Review of Biomedical Engineering

Abstract

The majority of therapeutics target membrane proteins, accessible on the surface of cells, to alter cellular signaling. Cells use membrane proteins to transduce signals into cells, transport ions and molecules, bind cells to a surface or substrate, and catalyze reactions. Newly devised technologies allow us to drug conventionally “undruggable” regions of membrane proteins, enabling modulation of protein–protein, protein–lipid, and protein–nucleic acid interactions. In this review, we survey the state of the art of high-throughput screening and rational design in drug discovery, and we evaluate the advances in biological understanding and technological capacity that will drive pharmacotherapy forward against unorthodox membrane protein targets.

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Crossref · 10.1146/annurev-bioeng-092115-025322

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Metadata

Authors
Yin, H., & Flynn, A. D.
Venue
Annual Review of Biomedical Engineering
Published
2016-07-11
Volume
18
Issue
1
Pages
51-76
ISSN
  • 1523-9829 (ISSN-L)
  • 1545-4274
OpenAlex
W2244890058
Cited by
339
References
142
FWCI
1.53
Type
journal article
Language
en
Open access
green

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CoChat. (2026). Citation check: Drugging Membrane Protein Interactions. https://app.cochat.ai/papers/10.1146/annurev-bioeng-092115-025322
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Yin, H., & Flynn, A. D. (2016). Drugging Membrane Protein Interactions. Annual Review of Biomedical Engineering. https://doi.org/10.1146/annurev-bioeng-092115-025322

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Bibliographic data: Semantic Scholar, OpenAlex, Crossref.

Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.