Use of 1-anilino-8-naphthalene-sulfonate as a probe of gastric vesicle transport
The Journal of Membrane Biology, ISSN: 0022-2631, Vol: 32, Issue: 1, Page: 301-318
1977
- 18Citations
- 5Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Metrics Details
- Citations18
- Citation Indexes18
- CrossRef18
- 10
- Captures5
- Readers5
Article Description
The interaction of 1-anilino-8-naphthalene-sulfonate (ANS) with vesicles derived from hog fundic mucosa was studied in the presence of valinomycin and with the addition of ATP. Evidence was found for two classes of sites, those rapidly accessible to ANS with a K of 7.5 μm and those slowly accessible, but rapidly accessed in the presence of valinomycin with a K of 2.5 μm. ATP transiently increases the quantum yield of the latter ANS binding sites only in the presence of valinomycin, but does not alter the number of K of those sites. The time course of this increase correlates with H uptake and Rb extrusion by those vesicles and H carriers such as tetrachlorsalicylanilide or nigericin abolish the ATP response. With ATP addition in the presence of SCN and valinomycin there is transient uptake of SCN. It is concluded that ANS is acting as a probe of a structural change dependent on a potential and H gradient. © 1977 Springer-Verlag New York Inc.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=0017331650&origin=inward; http://dx.doi.org/10.1007/bf01905224; http://www.ncbi.nlm.nih.gov/pubmed/17006; http://link.springer.com/10.1007/BF01905224; http://www.springerlink.com/index/pdf/10.1007/BF01905224; http://www.springerlink.com/index/10.1007/BF01905224; https://dx.doi.org/10.1007/bf01905224; https://link.springer.com/article/10.1007/BF01905224
Springer Science and Business Media LLC
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