ライフサイエンスコーパス: transport carrier

1 e lysosome for degradation by way of an AP-3 transport carrier.

2 ay mechanistic roles in the formation of the transport carrier.

3 l to the ER in coat protein complex I-formed transport carriers.

4 nd fission machineries to produce retrograde transport carriers.

5 assembly, a process essential for generating transport carriers.

6 g by promoting the biogenesis of TGN-derived transport carriers.

7 rt by controlling the biogenesis of specific transport carriers.

8 brane proteins by sorting them into membrane transport carriers.

9 exclude somatodendritic proteins from axonal transport carriers.

10 twork (TGN) of plasma membrane (PM)-destined transport carriers.

11 ed for the biogenesis of TGN to cell surface transport carriers.

12 ve face that seems to match the curvature of transport carriers.

13 an integral component of some intracellular transport carriers.

14 s of the secretory pathway by membrane-bound transport carriers.

15 is mediated by interactions between soluble transport carriers and insoluble NPC proteins that conta

16 nterface to locally concentrate COPII-coated transport carriers and link exit sites on the ER to ERGI

17 hondrial proteins functioning as precursors, transport carriers, and gates are preferentially degrade

18 this activity is used to control the size of transport carriers, and to prevent uncontrolled vesicula

19 At these locations, coated transport carriers are generated, with the Sar1 GTPase p

20 ur studies define a mechanism by which COPII transport carriers are retained locally at the ER/ERGIC

21 Membrane-bound transport carriers are used to transfer cargo between me

22 Quinone molecules are intracellular electron-transport carriers, as well as critical intra- and extra

23 This fission reaction is used to generate transport carriers at the TGN that are en route to the c

24 arly endosome, recycling endosome and apical transport carriers before reaching its steady-state apic

25 Retrograde transport carriers bud from the endosome coated by retro

26 ble cargo proteins are recognized by nuclear transport carriers, called importins, which mediate thei

27 estrates capture and packaging of cargo into transport carriers coated with sorting nexin BAR domain

28 e assembly of endoplasmic reticulum to Golgi transport carriers commences with the coating of specifi

29 s-Golgi network by regulating the fission of transport carriers destined for the plasma membrane.

30 e trans-Golgi network, regulating fission of transport carriers destined to the cell surface.

31 Our data reveal that growth of a mega transport carrier for collagen export from the ER is not

32 53)-containing membranes to generate a mega-transport carrier for export of collagens and apolipopro

33 end support to our suggestion that growth of transport carriers for exporting bulky cargoes requires

34 ed for the membrane fission that separates a transport carrier from its progenitor compartment: the l

35 formation of endoplasmic reticulum to Golgi transport carriers from endoplasmic reticulum sites clos

36 a, PKCeta, and PKD act in series to generate transport carriers from the TGN and their overactivation

37 ediated signaling regulates the formation of transport carriers from the TGN in mammalian cells.

38 released from a TGN block was colocalized in transport carriers in association with PI5K and actin co

39 was added exogenously to SMG via a membrane-transporting carrier in the presence of PI 3-kinase inhi

40 Nuclear transport carriers interact with proteins of the nuclear

41 Association of Ran x GTP with transport carriers (karyopherins) triggers the loading/u

42 ing studies indicated that these two nuclear transport carriers of different classes, p10 and Kap-bet

43 nvolves reduced endocytosis and/or increased transport carrier recruitment from an intracellular pool

44 eptor cells is mediated by rhodopsin-bearing transport carriers (RTCs) and regulated by the small GTP

45 i network (TGN) and regulates the fission of transport carriers specifically destined to the cell sur

46 Golgi network (TGN) regulates the fission of transport carriers specifically destined to the cell sur

47 R complexes into clathrin-coated vesicles or transport carriers (TCs) destined for delivery to endoso

48 p10/NTF2 is a nuclear transport carrier that mediates the uptake of cytoplasmi

49 mediates fusion of melanosomes with tubular transport carriers that also carry the cargo protein TYR

50 at PKD regulates the fission from the TGN of transport carriers that are en route to the cell surface

51 structural evolution of COPII (coat protein) transport carriers that are essential for the transport

52 pical and basolateral proteins into distinct transport carriers that emerge from the trans-Golgi netw

53 hat selects and packages cargo proteins into transport carriers that export cargo from the endosome.

54 pon warming, they exit these compartments in transport carriers that have very different membrane cha

55 sorting of proteins into distinct vesicular transport carriers that mediate secretion and interorgan

56 station for distinct apical and basolateral transport carriers that reach their respective surface d

57 m (ER) in two layers to generate cargo-laden transport carriers that ultimately fuse with an adjacent

58 nsfer from trans-Golgi network (TGN)-derived transport carriers to endosomes involves a still undefin

59 tes tethering and fusion of endosome-derived transport carriers to the trans-Golgi network (TGN).

60 We report here that COPII-coated transport carriers traverse a submicron, TFG (Trk-fused

61 ver, the role of large COPII vesicles as PC1 transport carriers was not unambiguously demonstrated.

62 GO1 remains at the neck of the newly forming transport carrier, which grows in size by addition of ER

63 at VAMP7 mediates fusion of BLOC-1-dependent transport carriers with melanosomes, illuminate SNARE re