Scopus Publication Detail
The publication detail shows the title, authors (with indicators showing other profiled authors), information on the publishing organization, abstract and a link to the article in Scopus. This abstract is what is used to create the fingerprint of the publication.
A large Ca2+-dependent channel formed by recombinant ADP/ATP carrier from Neurospora crassa resembles the mitochondrial permeability transition pore
Nickolay Brustovetsky; Maximilian Tropschug; Simone Heimpel; Doerthe Heidkämper; Martin Klingenberg (Profiled Author: Nikolai Broustovetski)
Biochemistry. 2002;41(39):11804-11811.
AbstractStrong support for the central role of the ADP/ATP carrier (AAC) in the mitochondrial permeability transition (mPT) is provided by the single-channel current measurements in patch-clamp experiments with the isolated reconstituted AAC. In previous work [Brustovetsky, N., and Klingenberg, M. (1996) Biochemistry 35, 8483-8488], this technique was applied to the AAC isolated from bovine heart mitochondria. Here we used recombinant AAC (rAAC) from Neurospora crassa expressed in E. coli, since AAC from mammalian sources cannot be expresssed in E. coli. The rAAC is free from residual mitochondrial components which might associate with the AAC in preparation from bovine heart. Ca2+-dependent channels with up to 600 pS are obtained, which are gated at > 150 mV. The channel corresponds to a preferential matrix-outside orientation of rAAC in the patch membrane as shown with carboxyatractylate and a polar gating asymmetry. The channel is inhibited by ADP and bongkrekate, not by carboxyatractylate. Cyclophilin, isolated from Neurospora crassa, suppresses the gating, thus increasing conductivity at high positive voltage. Cyclosporin A abolishes the cyclophilin effect. ADP does not eliminate the cyclophilin effect but produces fast large-amplitude flickering of the channel without a stable decrease of the channel conductance. Also the pro-oxidant tert-butyl hydroperoxide reversibly suppresses voltage gating of the channel. The results show that the AAC can be a conducting component of the mPT pore, exhibiting similar characteristics as the mPT pore (response to Ca2+, BKA, ADP), with a cyclophilin and pro-oxidant-sensitive gating at high voltage.
PMID: 12269823
Scientific Context
This section shows information related to the publication - computed using the fingerprint of the publication - including related publications, related experts with fingerprints representing significant amounts of overlap between their fingerprint and this publication. The red dots indicate whether those experts or terms appear within the publication, thereby showing potential and actual connections.
Related Publications
-
1.
2001Paul R. Territo; Stephanie A. French; Mary C. Dunleavy; Frank J. Evans; Robert S. Balaban
Journal of Biological Chemistry. 2001;276(4):2586-2599. -
2.
2004Simon J. Atkinson; Melanie A. Hosford; Bruce A. Molitoris
Mechanism of Actin Polymerization in Cellular ATP Depletion
Journal of Biological Chemistry. 2004;279(7):5194-5199. -
3.
2002Larry R. Jones; Razvan L. Cornea; Zhenhui Chen
Journal of Biological Chemistry. 2002;277(31):28319-28329.
Related Topics
Appears in this Document
Related Experts
Author of this Document
-
Internal ExpertsPublications
-
17









-
197









-
194









-
26









-
52











