The DOI matches its Crossref record; 3 of the 3 references it cites were found in a registry or an index.
Emerging issues of connexin channels: biophysics fills the gap
Abstract
1. Introduction 326 1.1 What? Terminology and general properties 327 1.2 Why? Reasons for biophysical study 329 1.3 How? Special issues for study of connexin channels 330 2. Molecular and structural context 331 2.1 Biochemical features 331 2.2 Structures 334 2.2.1 Junctional channels 335 2.2.2 Hemichannels 338 2.2.3 Heteromeric channels 342 2.2.4 Junctional plaques 347 3. Experimental approaches and issues specific to study of connexin channel physiology 349 3.1 Macroscopic currents 349 3.1.1 Junctional channels 349 3.1.2 Hemichannels 354 3.2 Single-channel currents 355 3.2.1 Junctional channels 355 3.2.2 Hemichannels 358 3.3 Molecular permeability 361 3.3.1 A selection of tracers 361 3.3.2 Junctional channels 362 3.3.3 Hemichannels 366 3.4 Other 367 4. Structural issues 368 4.1 What lines the pore? 368 4.2 Docking between hemichannels 373 4.2.1 Structural and molecular basis 374 4.2.2 Determinants of specificity of interaction 380 5. Permeability and selectivity 381 5.1 Among the usual ions 383 5.1.1 Unitary conductance 383 5.1.2 Selectivity 384 5.1.3 Nonlinear single-channel I–V relations and their molecular determinants 386 5.2 Among large permeants 391 5.2.1 Uncharged molecules 392 5.2.2 Charged molecules 393 5.2.3 Cytoplasmic/signaling molecules 396 6. Voltage sensitivity 399 6.1 Macroscopic transjunctional voltage sensitivity 404 6.2 Microscopic voltage sensitivity – Vj-gating 407 6.2.1 Molecular basis – voltage sensor 407 6.2.2 Molecular basis – transduction and/or state stability 409 6.3 Microscopic voltage sensitivity – loop gating 412 6.4 Vm-gating 414 7. Direct chemical modulation 415 7.1 Phosphorylation 417 7.2 Cytoplasmic pH and aminosulfonates 419 7.3 Calcium ion 424 7.4 Lipophiles 424 7.4.1 Long chain n-alkyl alcohols 425 7.4.2 Fatty acids and fatty acid amides 426 7.4.3 Halothane 426 7.5 Glycyrrhetinic acid and derivatives 427 7.6 Cyclic nucleotides 428 7.7 Other candidates 430 8. Connexinopathies 431 9. Summary 435 10. Acknowledgements 438 11. References 438 Connexins are the proteins that form the intercellular channels that compose gap junctions in vertebrates. Connexin channels mediate electrotonic coupling between cells and serve important functions as mediators of intercellular molecular signaling. Convincing demonstration of the latter function has been elusive, as have the experimental tools required for detailed functional study of the channels. Recently, substantial progress has been made on both fronts. Connexin channels are now known to be dynamic, multifunctional channels intimately involved in development, physiology and pathology, and amenable to study by state-of-the-art approaches. A host of developmental and physiological defects are caused by defects in connexin channels, and therefore in the intercellular molecular movement they mediate. The channel structure has been determined to 7·5 Å resolution within the plane of the membrane. Experimental paradigms have been developed that enable application of the tools of modern channel biophysics to study connexin channel structure–function. As a result, the biophysical mechanisms and biological functions of connexin channels now enjoy a vigorous and expanding experimental interest. This article focuses on the former, but with attention to issues likely to have biological consequences.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Chemical characterization of a family of brain lipids that induce sleep
Cravatt, B. F., Prospero-Garcia, O., Siuzdak, G., Gilula, N. B., Henriksen, S. J., Boger, D. L., & Lerner, R. A. (1995) · Science · doi:10.1126/science.7770779 · Cited by 620
Cotrina, M. L., Lin, J. H.-C., López-Garcı́a, J. C., Naus, C. C. G., & Nedergaard, M. (2000) · The Journal of Neuroscience · doi:10.1523/jneurosci.20-08-02835.2000 · Cited by 388
Solution Structure of the DNA Binding Domain of HIV-1 Integrase
Lodi, P. J., Ernst, J. A., Kuszewski, J., Hickman, A. B., Engelman, A., Craigie, R., Clore, G. M., & Gronenborn, A. M. (1995) · Biochemistry · doi:10.1021/bi00031a002 · Cited by 300
Cited by
ELECTRICAL SYNAPSES IN THE MAMMALIAN BRAIN
Connors, B. W., & Long, M. A. (2004) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.26.041002.131128 · Cited by 784
Remodelling of gap junctions and connexin expression in diseased myocardium
Severs, N. J., Bruce, A. F., Dupont, E., & Rothery, S. (2008) · Cardiovascular Research · doi:10.1093/cvr/cvn133 · Cited by 560
Connexin channel permeability to cytoplasmic molecules
Harris, A. L. (2007) · Progress in Biophysics and Molecular Biology · doi:10.1016/j.pbiomolbio.2007.03.011 · Cited by 455
Connexin 30 sets synaptic strength by controlling astroglial synapse invasion
Pannasch, U., Freche, D., Dallérac, G., Ghézali, G., Escartin, C., Ezan, P., Cohen-Salmon, M., Benchenane, K., Abudara, V., Dufour, A., et al. (2014) · Nature Neuroscience · doi:10.1038/nn.3662 · Cited by 329
Connexin37 protects against atherosclerosis by regulating monocyte adhesion
Wong, C. W., Christen, T., Roth, I., Chadjichristos, C. E., Derouette, J.-P., Foglia, B. F., Chanson, M., Goodenough, D. A., & Kwak, B. R. (2006) · Nature Medicine · doi:10.1038/nm1441 · Cited by 273
Metadata
- Authors
- L. Harris, A.
- Venue
- Quarterly Reviews of Biophysics
- Publisher
- Cambridge University Press (CUP)
- Published
- 2001-08
- Volume
- 34
- Issue
- 3
- Pages
- 325-472
- ISSN
- 0033-5835 (ISSN-L)
- 1469-8994
- OpenAlex
- W2161194374
- Cited by
- 800
- References
- 3
- FWCI
- 11.94
- Type
- journal article
- Language
- en
- Open access
- closed
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review
How to cite
Cite CoChat for the checks on this page, and the paper for its own findings.
- This page
- CoChat. (2026). Citation check: Emerging issues of connexin channels: biophysics fills the gap. https://app.cochat.ai/papers/10.1017/s0033583501003705
- The paper
- L. Harris, A. (2001). Emerging issues of connexin channels: biophysics fills the gap. Quarterly Reviews of Biophysics. https://doi.org/10.1017/s0033583501003705
Data sources
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.