ライフサイエンスコーパス: NLS peptide

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1 e fed a high-fat diet), i.p., 0.13 mumol/day NLS peptide administration for 5 weeks attenuated NF-kap

2 NLS peptide also attenuated pro-inflammatory gene expres

3 The NLS peptide, although largely unfolded, has a weak tende

4 Docking is not inhibited by an NLS peptide and does not require importins/karyopherins,

5 is development and identifies cell-permeable NLS peptide as a potential anti-atherosclerotic agent.

6 in the absence and presence of a monopartite NLS peptide at 2.2 A and 2.8 A resolution, respectively.

7 RME and NLS; and (5) the adenovirus RME and NLS peptides attached to the nanoparticle as separate pi

8 he importin-alpha aggregation is relieved by NLS peptide binding, with the importin-alpha then bindin

9 thermal sensitivity, as assayed by in vitro NLS peptide binding.

10 t were determined by an in vitro assay using NLS peptide-conjugated bovine serum albumin (NLS-BSA) or

11 STAT1 in Jurkat T cells can be regulated by NLS peptide delivered noninvasively to the cytoplasm of

12 amounts of the nuclear localization signal (NLS) peptide from simian virus 40 large T antigen, sugge

13 Cross-linking experiments with free NLS peptides in HeLa cytosol indicated that each peptide

14 When unphosphorylated, the "CDK/NLS" peptides inhibit T-antigen assembly and bind non-se

15 Correspondingly, NLS peptide inhibits the nuclear migration of MA but not

16 Further, we show that inhibitory NLS peptide interacts in vitro with a cytoplasmic NLS re

17 NLS peptide-mediated disruption of the nuclear import of

18 Binding of the NLS peptide occurs at two sites within a helical surface

19 ession with the nuclear localization signal (NLS) peptide of SV40, shows reduced enzyme activity when

20 to the purified importin-alpha aggregation, NLS peptides relieve the aggregation of importin-alpha i

21 NLS peptide significantly inhibited lesion development a

22 ascular smooth muscle cells and macrophages, NLS peptide specifically blocked the importin alpha-medi

23 the peptide IFN-gamma(95-132) and the SV40 T-NLS peptide, suggesting that intact IFN-gamma was also t

24 hown to possess nuclear localization signal (NLS) peptides, the subcellular distribution of neither G

25 This indicates that both D- and L-form NLS peptides use the same import machinery.

26 For example, particles modified solely with NLS peptides were not able to target the nucleus of HepG

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