共查询到20条相似文献,搜索用时 31 毫秒
1.
S. Fujino K. Satoh T. Bando T. Kurokawa T. Nakai K. Takashima M. Fujino 《Cellular and molecular life sciences : CMLS》1989,45(5):466-469
Summary A new glycoprotein of 31,500 dalton, which has a high affinity for ouabain, and is independent of (Na+–K+)-ATPase, was solubilized from transverse tubule membrane and junctional sarcoplasmic reticulum complexes (TTM-JSR) of cat cardiac muscle. This protein could be extracted only in small amounts from sarcolemmaplasma membrane (SLM-PL) fragments, suggesting that it indeed originates from the TTM-JSR. 相似文献
2.
S. Fujino K. Satoh T. Nakai K. Togashi T. Kado M. Fujino T. Arima M. Fujino 《Cellular and molecular life sciences : CMLS》1993,49(2):138-144
The excitation-contraction (E-C) coupling process in single twitch fibres from frog toe muscle was inhibited selectively by phenylglyoxal (PGO), a specific guanidyl modifying reagent. A new protein (31.5 kDa), which has PGO-binding ability and seems to play a key role in the E-C coupling process, was solubilized from transverse tubule membrane-junctional sarcoplasmic reticulum complexes (TTM-JSR) of frog skeletal muscles, using14C-PGO. The monoclonal antibody against this protein applied extracellularly inhibited the E-C coupling process of the single fibres. This protein appears to constitute the very first step of input for E-C coupling. It is considered to behave as an indispensable part of an electrometer to measure membrane potentials. Therefore, the name electrometrin is suggested for the new protein. 相似文献
3.
The specific activity of dipeptidyl peptidase IV (DPP IV E.C. 3.4.14.-) in the plasma membrane of Morris hepatoma 9121 or hepatoma 7777 was 3.5% and 2.9%, respectively, of that in the plasma membrane of rat liver. The enzyme activity in the serum of hepatoma-bearing rats was 141% (hepatoma 91219) and 162% (hepatoma 7777) of the normal value. Cytochemical investigation showed that the DPP IV activity was almost completely absent from the hepatoma cell plasma membrane and was not sequestered within these cells. Indirect immunofluorescence staining with a polyclonal antibody directed against DPP IV indicated that the loss of activity was due to the absence of DPP IV molecules in the plasma membrane. The possibility that the enzyme is transferred from the membrane into the serum as a result of structural alterations is discussed. 相似文献
4.
C. Hanski T. Zimmer R. Gossrau W. Reutter 《Cellular and molecular life sciences : CMLS》1986,42(7):826-828
Summary The specific activity of dipeptidyl peptidase IV (DPPIV E.C. 3.4.14.-) in the plasma membrane of Morris hepatoma 9121 or hepatoma 7777 was 3.5% and 2.9%, respectively, of that in the plasma membrane of rat liver. The enzyme activity in the serum of hepatoma-bearing rats was 141% (hepatoma 91219) and 162% (hepatoma 7777) of the normal value. cytochemical investigation showed that the DPP IV activity was almost completely absent from the hepatoma cell plasma membrane and was not sequestered within these cells. Indirect immunofluorescence staining with a polyclonal antibody directed against DPP IV indicated that the loss of activity was due to the absence of DPP IV molecules in the plasma membrane. The possibility that the enzyme is transferred from the membrane into the serum as a result of structural alterations is discussed. 相似文献
5.
Seaman MN 《Cellular and molecular life sciences : CMLS》2008,65(18):2842-2858
The steady-state localisation of membrane proteins in the endocytic system is the result of many sorting events that occur
at various points throughout the endosomal pathway. A protein that has been endocytosed from the plasma membrane or sorted
at the trans-Golgi network (TGN) and transported to an endosome will ultimately be delivered to one of three destinations:
the plasma membrane, the TGN or the lysosome. Where a membrane protein is trafficked to depends on the interactions between
sorting motifs present in the membrane protein and the machinery that can decode these motifs. Much of the protein machinery
that recognises sorting motifs is conserved from yeast toman, and in this review I will discuss this machinery and the motifs
that govern endosomal protein sorting. (Part of a Multi-author Review) 相似文献
6.
Amaiden MR Santander VS Monesterolo NE Campetelli AN Rivelli JF Previtali G Arce CA Casale CH 《Cellular and molecular life sciences : CMLS》2011,68(10):1755-1768
The presence of tubulin in human erythrocytes was demonstrated using five different antibodies. Tubulin was distributed among
three operationally distinguishable pools: membrane, sedimentable structure and soluble fraction. It is known that in erythrocytes
from hypertensive subjects (HS), the Na+, K+-ATPase (NKA) activity is partially inhibited as compared with erythrocytes from normal subjects (NS). In erythrocytes from
HS the membrane tubulin pool is increased by ~150%. NKA was found to be forming a complex with acetylated tubulin that results
in inhibition of enzymes. This complex was also increased in erythrocytes from HS. Treatment of erythrocytes from HS with
nocodazol caused a decrease of acetylated tubulin in the membrane and stimulation of NKA activity, whereas taxol treatment
on erythrocytes from NS had the opposite effect. These results suggest that, in erythrocytes from HS, tubulin was translocated
to the membrane, where it associated with NKA with the consequent enzyme inhibition. 相似文献
7.
J. Moraczewski J. Gautron A. Duma A. Le Moigne I. Martelly 《Cellular and molecular life sciences : CMLS》1991,47(3):241-245
Summary The relationship between the activity of protein kinase C (PKC) and muscle innervation was explored in the rat sternomastoid muscle (SM) from day 18 of gestation (E18) to adult age. Between E18 and birth, PKC activity rose 5-fold, and during the day after birth, diminished to a level characteristic of the mature muscle. The rise chiefly occurred in the neural part of the muscle, in both the membrane and the cytosol fractions. Between E18 and day 5 after birth, the ratios of membrane to cytosol PKC activity rose from 0.5 to 10 and 3 respectively in the neural and aneural parts of the muscle. Denervation of adult SM reduced PKC activity by half in the membrane fraction of the neural part but did not significantly change it in the membrane or cytosol fractions of the aneural parts. These results suggest that innervation plays an important part in determining the level of PKC activity in muscle. 相似文献
8.
The relationship between the activity of protein kinase C (PKC) and muscle innervation was explored in the rat sternomastoid muscle (SM) from day 18 of gestation (E18) to adult age. Between E18 and birth, PKC activity rose 5-fold, and during the day after birth, diminished to a level characteristic of the mature muscle. The rise chiefly occurred in the neural part of the muscle, in both the membrane and the cytosol fractions. Between E18 and day 5 after birth, the ratios of membrane to cytosol PKC activity rose from 0.5 to 10 and 3 respectively in the neural and aneural parts of the muscle. Denervation of adult SM reduced PKC activity by half in the membrane fraction of the neural part but did not significantly change it in the membrane or cytosol fractions of the aneural parts. These results suggest that innervation plays an important part in determining the level of PKC activity in muscle. 相似文献
9.
Subcellular distribution of total phospholipids and mannophosphoinositides (mannosides) was examined in Mycobacterium smegmatis ATCC 607 during its transition from the early exponential to the stationary phase of growth. There was relatively more of these substances in the cell membrane than in the cell wall, and the total amount increased with the age of the culture. Among individual mannosides, dimannophosphoinositides (dimannosides) were distributed equally in the cell wall and membrane. However, hexamannophosphoinositides (hexamannosides) were more predominant in the cell membrane, and the level increased with the age of the culture. 相似文献
10.
Cyclic AMP phosphodiesterase (PDE) in membrane fraction from rat cerebral cortex was activated by Triton X-100, and treatment at alkaline pH and with phospholipase C. These results suggest that membrane PDE exists in a latent form and is influenced by microenvironmental changes within the membrane. Furthermore, the PDE, unlike soluble enzyme, is not influenced by a protein activator and Ca++. 相似文献
11.
Robert Renthal 《Cellular and molecular life sciences : CMLS》2010,67(7):1077-1088
Polytopic α-helical membrane proteins cannot spontaneously insert into lipid bilayers without assistance from polytopic α-helical
membrane proteins that already reside in the membrane. This raises the question of how these proteins evolved. Our current
knowledge of the insertion of α-helices into natural and model membranes is reviewed with the goal of gaining insight into
the evolution of membrane proteins. Topics include: translocon-dependent membrane protein insertion, antibiotic peptides and
proteins, in vitro insertion of membrane proteins, chaperone-mediated insertion of transmembrane helices, and C-terminal tail-anchored
(TA) proteins. Analysis of the E. coli genome reveals several predicted C-terminal TA proteins that may be descendents of proteins involved in pre-cellular membrane
protein insertion. Mechanisms of pre-translocon polytopic α-helical membrane protein insertion are discussed. 相似文献
12.
Tetraspanins regulate a variety of cellular functions. However, the general cellular mechanisms by which tetraspanins regulate these functions remain poorly understood. In this article we collected the observations that tetraspanins regulate the formation and/or development of various tubular structures of cell membrane. Because tetraspanins and their associated proteins (1) are localized at the tubular structures, such as the microvilli, adhesion zipper, foot processes, and penetration peg, and/or (2) regulate the morphogenesis of these membrane tubular structures, tetraspanins probably modulate various cellular functions through these membrane tubular structures. Some tetraspanins inhibit membrane tubule formation and/or extension, while others promote them. We predict that tetraspanins regulate the formation and/or development of various membrane tubular structures: (1) microvilli or nanovilli at the plasma membranes free of cell and matrix contacts, (2) membrane tubules at the plasma membrane of cell-matrix and cell-cell interfaces, and (3) membrane tubules at the intracellular membrane compartments. These different membrane tubular structures likely share a common morphogenetic mechanism that involves tetraspanins. Tetraspanins probably regulate the morphogenesis of membrane tubular structures by altering (1) the biophysical properties of the cell membrane such as curvature and/or (2) the membrane connections of cytoskeleton. Since membrane tubular structures are associated with cell functions such as adhesion, migration, and intercellular communication, in all of which tetraspanins are involved, the differential effects of tetraspanins on membrane tubular structures likely lead to the functional difference of tetraspanins. 相似文献
13.
A. Baba T. Tsukamoto T. Matsuda H. Iwata 《Cellular and molecular life sciences : CMLS》1978,34(9):1139-1140
Summary Cyclic AMP phosphodiesterase (PDE) in membrane fraction from rat cerebral cortex was activated by Triton X-100, and treatment at alkaline pH and with phospholipase C. These results suggest that membrane PDE exists in a latent form and is influenced by microenvironmental changes within the membrane. Furthermore, the PDE, unlike soluble enzyme, is not influenced by a protein activator and Ca++. 相似文献
14.
S Batra 《Experientia》1986,42(6):608-611
Specific binding of tritiated quinuclidinyl benzilate (3H-QNB) to surface membrane muscarinic receptors was utilized to identify plasma membrane (PM) fractions from smooth muscle of the rabbit urinary bladder. Accumulation of 3H-QNB in the PM fraction was 4-5-fold higher than that in fractions of endoplasmic reticulum (EM) or mitochondria (M). A similar pattern of distribution was found for 5'-nucleotidase. 3H-QNB binding therefore appears to be a suitable marker for plasma membrane of the urinary bladder. Data on ATP-dependent calcium uptake by PM and ER fractions showed that oxalate highly potentiated calcium uptake by both fractions and consequently this feature cannot be used to identify ER fractions specifically. 相似文献
15.
We have recently demonstrated, using electron paramagnetic resonance (EPR) spectroscopy, that insulin receptor internalization in response to insulin incubation (down-regulation) in human erythrocytes is accompanied by a transient decrease in membrane order, as measured by the 2T' parallel order parameter. Since membrane lipids play such an important role in receptor internalization, we investigated the possible effects that an alteration of the normally-occurring lipid profile might have on down-regulation and the concomitant transient decrease in membrane order. Consequently, human erythrocytes enriched with cholesterol and erythrocytes from cirrhotic patients were examined, because both of these groups of cells have a higher cholesterol/phospholipid molar ratio (CH/PL) than controls. The 5-nitroxystearate spin label, which inserts into the lipid bilayer of cell membranes, was used to monitor changes in 2T' parallel for a 3-h period at 37 degrees C. We report here that both cholesterol-enriched and cirrhotic erythrocytes do not down-regulate, as demonstrated by binding assays, and that they do not show the typical transient decrease in membrane order observed in controls. The results seem to indicate that a more ordered membrane inhibits internalization of the insulin receptor in erythrocytes, and that an increase in membrane disorder is necessary for insulin receptor down-regulation. 相似文献
16.
Trimeric guanine nucleotide-binding proteins (G proteins) function as the key regulatory elements in a number of transmembrane
signaling cascades where they convey information from agonist-activated receptors to effector molecules. The subcellular localization
of G proteins is directly related to their functional role, i.e., the dominant portion of the cellular pool of G proteins
resides in the plasma membrane. An intimate association of G protein subunits with the plasma membrane has been well known
for a long time. However, results of a number of independent studies published in the past decade have indicated clearly that
exposure of intact target cells to agonists results in subcellular redistribution of the cognate G proteins from plasma membranes
to the light-vesicular membrane fractions, in internalization from the cell surface into the cell interior and in transfer
from the membrane to the soluble cell fraction (high-speed supernatant), i.e., solubilization. Solubilization of G protein
α subunits as a consequence of stimulation of G protein-coupled receptors (GPCRs) with agonists has also been observed in
isolated membrane preparations. The membrane-cytosol shift of G proteins was detected even after direct activation of these
proteins by non-hydrolyzable analogues of GTP or by cholera toxin-induced ADP-ribosylation. In addition, prolonged stimulation
of GPCRs with agonists has been shown to lead to down-regulation of the relevant G proteins. Together, these data suggest
that G proteins might potentially participate in a highly complex set of events, which are generally termed desensitization
of the hormone response. Internalization, subcellular redistribution, solubilization, and down-regulation of trimeric G proteins
may thus provide an additional means (i.e., beside receptor-based mechanisms) to dampen the hormone or neurotransmitter response
after sustained (long-term) exposure.
Received 31 August 2001; received after revision 31 October 2001; accepted 7 November 2001 相似文献
17.
Iness Charfi Khaled Abdallah Louis Gendron Graciela Pineyro 《Cellular and molecular life sciences : CMLS》2018,75(12):2257-2271
Soon after internalization delta opioid receptors (DOPrs) are committed to the degradation path by G protein-coupled receptor (GPCR)-associated binding protein. Here we provide evidence that this classical post-endocytic itinerary may be rectified by downstream sorting decisions which allow DOPrs to regain to the membrane after having reached late endosomes (LE). The LE sorting mechanism involved ESCRT accessory protein Alix and the TIP47/Rab9 retrieval complex which supported translocation of the receptor to the TGN, from where it subsequently regained the cell membrane. Preventing DOPrs from completing this itinerary precipitated acute analgesic tolerance to the agonist DPDPE, supporting the relevance of this recycling path in maintaining the analgesic response by this receptor. Taken together, these findings reveal a post-endocytic itinerary where GPCRs that have been sorted for degradation can still recycle to the membrane. 相似文献
18.
S. Batra 《Cellular and molecular life sciences : CMLS》1986,42(6):608-611
Summary Specific binding of tritiated quinuclidinyl benzilate (3H-QNB) to surface membrane muscarinic receptors was utilized to identify plasma membrane (PM) fractions from smooth muscle of the rabbit urinary bladder. Accumulation of3H-QNB in the PM fraction was 4–5-fold higher than that in fractions of endoplasmic reticulum (EM) or mitochondria (M). A similar pattern of 相似文献
19.
F Chany-Fournier A Pauloin C Chany 《Comptes rendus des séances de l'Académie des sciences. Série D, Sciences naturelles》1977,285(8):941-944
A tissue antagonist of interferon (TAI) extracted from mouse costal cartilage contains a substance which has many properties characteristic of plant lectins. After binding to the cell membrane receptors, it agglutines normal and transformed murine cells. In interferon treated cells, it restores virus sensitivity probably through a modification in the distribution of membrane bound cellular antigens. 相似文献
20.
The activation and signalling activity of the membrane μ-opioid receptor (MOP-R) involve interactions among the receptor,
G-proteins, effectors and many other membrane or cytosolic proteins. Decades of investigation have led to identification of
the main biochemical processes, but the mechanisms governing the successive protein–protein interactions have yet to be established.
We will need to unravel the dynamic membrane organisation of this complex and multifaceted molecular machinery if we are to
understand these mechanisms. Here, we review and discuss advances in our understanding of the signalling mechanism of MOP-R
resulting from biochemical or biophysical studies of the organisation of this receptor in the plasma membrane. 相似文献