نتایج جستجو برای: channel protein

تعداد نتایج: 1431603  

Journal: :Bioscience reports 2010
Zhiliang Cheng

Special codes are embedded in the primary sequence of newly synthesized proteins to determine their final destination. Protein translocation across biological membranes requires co-operation between the targeting and translocation machineries. A conserved membrane channel, the Sec61/SecY complex, mediates protein translocation across or integration into the endoplasmic reticulum membrane in euk...

2017
Debebe Gebremedhin David X Zhang Dorothee Weihrauch Nnamdi N Uche David R Harder

The transient receptor potential vallinoid type 4 (TRPV4) is a calcium entry channel known to modulate vascular function by mediating endothelium-dependent vasodilation. The present study investigated if isolated cerebral arterial myocytes of the Fawn Hooded hypertensive (FHH) rat, known to display exaggerated KCa channel current activity and impaired myogenic tone, express TRPV4 channels at th...

2012
Donna L. Cioffi Songwei Wu Hairu Chen Mikhail Alexeyev Claudette M. St. Croix Bruce R. Pitt Stefan Uhlig Troy Stevens

Rationale: Canonical transient receptor potential 4 (TRPC4) contributes to the molecular composition of a channel encoding for a calcium selective store-operated current, ISOC, whereas Orai1 critically comprises a channel encoding for the highly selective calcium release activated calcium current, ICRAC. However, Orai1 may interact with TRPC proteins and influence their activation and permeatio...

Journal: :Circulation research 2012
Donna L Cioffi Songwei Wu Hairu Chen Mikhail Alexeyev Claudette M St Croix Bruce R Pitt Stefan Uhlig Troy Stevens

RATIONALE Canonical transient receptor potential 4 (TRPC4) contributes to the molecular composition of a channel encoding for a calcium selective store-operated current, I(SOC), whereas Orai1 critically comprises a channel encoding for the highly selective calcium release activated calcium current, I(CRAC). However, Orai1 may interact with TRPC proteins and influence their activation and permea...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2009
Hee Jung Chung Xiang Qian Melissa Ehlers Yuh Nung Jan Lily Yeh Jan

G protein-activated inwardly rectifying K(+) (GIRK) channels regulate neuronal excitability by mediating inhibitory effects of G protein-coupled receptors for neurotransmitters and neuromodulators. Notwithstanding many studies reporting modulation of GIRK channel function, whether neuronal activity regulates GIRK channel trafficking remains an open question. Here we report that NMDA receptor ac...

Journal: :Cell 2010
Adi Raveh Ayelet Cooper Liora Guy-David Eitan Reuveny

G protein-coupled receptors (GPCRs) respond to agonists to activate downstream enzymatic pathways or to gate ion channel function. Turning off GPCR signaling is known to involve phosphorylation of the GPCR by GPCR kinases (GRKs) to initiate their internalization. The process, however, is relatively slow and cannot account for the faster desensitization responses required to regulate channel gat...

Journal: :EMBO reports 2009
Kush Dalal Franck Duong

Protein translocation across the bacterial membrane occurs at the SecY complex or channel. The resting SecY channel is impermeable to small molecules owing to a plug domain that creates a seal. Here, we report that a channel loosely sealed, or with a plug locked open, does not, however, lead to general membrane permeability. Instead, strong selectivity towards small monovalent anions, especiall...

Journal: :The Journal of biological chemistry 1997
S M Valenzuela D K Martin S B Por J M Robbins K Warton M R Bootcov P R Schofield T J Campbell S N Breit

Ion channels are known to be present on the plasma membrane of virtually all cells and have been found on the membranes of various intracellular organelles. However, until recently they were believed not to occur at the nuclear membrane. In this study we describe the molecular cloning and characterization of a nuclear ion channel protein, designated nuclear chloride channel-27 (NCC27), from the...

Journal: :Circulation 2001
G Münch B Bölck A Sugaru K Brixius W Bloch R H Schwinger

BACKGROUND The sarcoplasmic reticulum (SR) Ca(2+)-release channel plays a key role in the excitation-contraction coupling of cardiac myocytes. Because respective alterations have been reported in human heart failure, we investigated isoform expression of the SR Ca(2+)-release channel in human hearts from patients with terminal heart failure (dilated cardiomyopathy [DCM], n=8) and nonfailing org...

2005
J. J. Matsuda

Voltage-dependent sodium channels from a variety of tissues are known to be phosphorylated by the cAMP-dependent protein kinase, protein kinase A. However, the functional significance of sodium channel phosphorylation is not clearly understood. Using whole-cell voltage-clamp techniques, we show that sodium currents (INaS) in rabbit cardiac myocytes are enhanced by isoproterenol (ISO). This enha...

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