ライフサイエンスコーパス: A-band

1 A band at 3642 cm(-1) in BPR, assigned to the OH stretch

2 A band at 38 kDa reacted with MAb 1.1 whereas a band at

3 A band detected at 1996 cm(-1) in the CO-flushed enzyme

4 A band extracted from a differential display polyacrylam

5 A band gap at the Fermi level, as expected for a Zintl p

6 A band gap of 0.12(2) eV was determined by reflectance s

7 A band in the appropriate molecular weight range was ide

8 A band of 73 kDa was increased in striatal membranes.

9 A band of chondrocytes adjacent to the developing interz

10 A band of free polyP was also visible, suggesting that p

11 A band of heavily labeled, medium-sized CB-immunoreactiv

12 A band of reduced reflectivity below the RPE was identif

13 A band of Reelin-positive cells filled the superficial d

14 A band of the same size was also immunopurified from hum

15 A band shift assay was designed to evaluate the influenc

16 A band with the p40 electrophoretic mobility was found t

17 A band-sharing index indicating relatedness was created

18 s show efficient blue (15 A) or green (25-40 A) band-edge photoemission with luminescence quantum yie

19 he bulk region merges to vacuum over a ca. 5 A band with progressive diminution of the density and hy

20 ne another, and progressed to small, aligned A-band-sized aggregates.

21 of second harmonic generation, which allows A-bands to be imaged independently of T-tubule morpholog

22 KLHL40 localizes to the sarcomere I band and A band and binds to nebulin (NEB), a protein frequently

23 sarcomeric locations, I band in the IFM and A band in synchronous muscles.

24 The observed trends for the amide I-III and A bands obtained by single-pass ATR-FT-IR agreed with th

25 required for the assembly of the M-band and A-band and for the regular alignment of the network SR a

26 urin destabilizes proteins of the M-band and A-band but not of the Z-disk.

27 cteristics of sparks found in the Z-line and A-band zones were very similar, whereas sparks from the

28 M-bands and A-bands, but not Z-disks or I-bands, were disrupted when

29 embly, including the assembly of Z-discs and A-bands, but not for early steps such as the assembly of

30 nd PCAF associate with the Z-disc and I- and A-bands of cardiac sarcomeres.

31 I- and A-bands were clearly observed, and thick filaments were

32 action contributes to the assembly of M- and A-bands.

33 ugar chains, the homopolymer common antigen (A band) and the heteropolymer O antigen (B band), which

34 SN-5 antibody colocalized with paramyosin at A-bands in wild type and colocalized with abnormal accum

35 Genetic deletion of the I-band-A-band junction (IAjxn) in titin increases strain on the

36 tin type 3 domains that comprises the I-band/A-band (IA) junction and obtained a viable mouse model.

37 ducing myofibrils with well defined I bands, A bands, and H zones.

38 e discuss the possible relationships between A-band arrangements in successive sarcomeres along a myo

39 the spacing between centroids of contiguous A-bands.

40 The different A-band organisation in flies compared with Lethocerus, w

41 attice of myosin filaments in the Drosophila A-band.

42 In the relaxed state, the dynamic A-band lattice spacing change as a result of a 2 % step

43 ansients and disrupts myosin thick filament (A band) assembly.

44 tis elegans, the gene unc-89 is required for A-band organization of striated muscle.

45 ously excite second harmonic generation from A-bands of myofibrils and 2-photon fluorescence from flu

46 t the same nine axial positions in each half A-band, consistent with a circumferential and/or radial

47 116 nm, are axially shifted in the hexagonal A-band lattice by one-third of the 14.5 nm axial spacing

48 arranged systematically within the hexagonal A-band lattice of myosin filaments, can redistribute thr

49 hown to increase myosin rod length, increase A-band and sarcomere length, and decrease flight perform

50 responds to mainly physiologically inelastic A-band part of the protein, and for a proteolytic fragme

51 med, the muscle myosin became organized into A-bands, and the cells began beating.

52 which thick filaments are not organized into A-bands, and there are no M-lines.

53 Structurally, the longer A-band and sarcomere lengths found in the hinge B myofib

54 h of the 1.6 mum filaments present in mature A-bands.

55 wever, EM of muscle fibers showed misaligned A-bands.

56 the actin filaments in the bony fish muscle A-band cell unit.

57 e systematically arranged in the fish muscle A-band lattice relative to the myosin head positions, an

58 of troponin molecules in the resting muscle A-band.

59 each half of the vertebrate striated muscle A-band.

60 dicating that they all arise from the muscle A-band.

61 hin is a giant polypeptide located in muscle A-bands.

62 unc-89 results in disorganization of muscle A-bands.

63 Adjacent myosin filaments in striated muscle A-bands are cross-linked by the M-band.

64 tion requires the presence of B-band but not A-band lipopolysaccharide.

65 A novel A-band titin mutation, c.92167C>T (p.P30723S), was found

66 us for the FINmaj TMD mutation and the novel A-band titin missense mutation showed a phenotype comple

67 ts interspersed within the overlap region of A bands and even within the H zone.

68 ere stretch therefore results in movement of A-band titin with respect to the thick filament backbone

69 The stiffness of A-band titin was found to be high, relative to that of I

70 to obtain the axial density distribution of A-bands in electron micrographs of well-preserved specim

71 d around Z-disk analogues and to the edge of A-bands.

72 y, this antiserum localizes to the middle of A-bands, consistent with UNC-89 being a structural compo

73 -C and -D isoforms localize to the middle of A-bands, like previously-described UNC-89 antibodies, an

74 of MyBP-C slow that reside in the C-zones of A-bands, variant-1 preferentially concentrates around M-

75 s in the Ca2+ content of the mitochondria or A band.

76 roduction in a pslB mutant and pslB promoted A-band LPS synthesis in a wbpW mutant, indicating functi

77 was determined by integrating the respective A-band intensity peak and computing the location at whic

78 with image processing confirm that the same A-band superlattice occurs in all of these flies; it may

79 e strain-sensing via titin in the sarcomeric A-band as the basis for length-dependent activation, tit

80 alize the protein with MHC to the sarcomeric A-band in immunostained muscles.

81 ion of UNC-89 is to help organize sarcomeric A-bands, especially M-lines.

82 We show that cardiac and skeletal A-bands are very similar, with a length of 1.58+/-0.01 m

83 functionally belongs to the relatively stiff A-band region of titin.

84 It is noteworthy that A-band LPS is selectively maintained on the P. aeruginos

85 In the variant S65T/H148D, the A band absorbance maximum is red-shifted to approximatel

86 concomitant with crossbridge binding in the A band.

87 calization from the Z band to the tip of the A band in these muscles.

88 7 to 9 transverse lines in a portion of the A band where crossbridges are found (C zone).

89 es, we found that HDAC3 was localized to the A band of sarcomeres and was capable of deacetylating my

90 etailed in the accompanying papers, when the A band is excited, green fluorescence appears with a ris

91 fferent kinetics are measured in each of the A bands for times shorter than the characteristic time o

92 ized by immunofluorescence microscopy to the A bands of body-wall muscles, but not the pharynx.

93 the myosin molecules represented within the A bands.

94 that, in addition to interference across the A-band, which must be occurring, the observed meridional

95 cells, has the same primary sequence as the A-band O antigen of Pseudomonas aeruginosa, except that

96 us work on single rigor cross-bridges at the A-band periphery where the myosin concentration is low s

97 -band architecture and also localizes at the A-band, where it interacts with both actin and myosin to

98 calized at the Z-line, whereas OGA is at the A-band.

99 ults indicate that titin compresses both the A-band and Z-disk lattice spacing with viscoelastic beha

100 By EM, the A-band and both Z-band lattice spacings varied with temp

101 f Pseudomonas aeruginosa PAO1 (expresses the A-band and B-band of O antigen) and AK1401 (expresses th

102 band of O antigen) and AK1401 (expresses the A-band but not the B-band) to silicon were investigated

103 main pairs A164-A165 and A168-A169, from the A-band of the giant muscle protein titin, reveal that th

104 and discuss the transition of titin from the A-band to the Z-band.

105 filament lattice spacing was measured in the A-band (d(1,0)) and Z-disk (d(Z)) regions of the sarcome

106 equencing, we explain why truncations in the A-band domain of TTN cause DCM, whereas truncations in t

107 on is low suggests molecular crowding in the A-band promotes occupancy of the straight myosin conform

108 oncept of cardiac troponin I function in the A-band region of the sarcomere and potential signaling t

109 in the hexagonal lattice of filaments in the A-band.

110 ows for the usual elastic positioning of the A-band in the final sarcomere, whereas the transduction

111 nd and may extend into the outer edge of the A-band in the obliquely striated muscle of the nematode.

112 the integrity and central positioning of the A-band in the sarcomere and it may act as a template upo

113 ccessory protein stripes in each half of the A-band spaced axially at 43-nm intervals and starting at

114 There must be structural features of the A-band that have not yet been described.

115 bout 1 nm inwards (towards the center of the A-band) at low velocity shortening (around 0.9 T0): thei

116 the myosin heads, at least at the end of the A-band.

117 nine sites, 43nm apart, in each half of the A-band.

118 and skeletal muscles and compare this to the A-band structure in cardiac muscle of MyBP-C-deficient m

119 We observed a small volume within the A-band ( approximately 10(-15) L) by confocal microscopy

120 nvestigate the distribution of MyBP-C in the A-bands of cardiac and skeletal muscles and compare this

121 olecules of the giant protein titin span the A-bands and I-bands that make up striated muscle.

122 binding region fails to localize throughout A-bands.

123 iomyopathy were overrepresented in the titin A-band but were absent from the Z-disk and M-band region

124 um mapped the AB105 antigen predominantly to A bands of myofibrils within Purkinje fibers.

125 alyses, we found that HDAC3 was localized to A-band of sarcomeres and capable of deacetylating myosin

126 nsverse striations that are in register with A-bands.