ライフサイエンスコーパス: peptide aptamer

1 le ligand control over the presentation of a peptide aptamer.

2 , comparable with that of recently described peptide aptamers.

3 ajor Geminiviridae genera and identified two peptide aptamers (A22 and A64) that interact strongly wi

4 We identified peptide aptamers against Dishevelled (Dsh) and beta-cate

5 ation-specific surface immobilization of the peptide aptamer and to ensure exposure of the binding si

6 cificity in kinetic analysis biomechanics in peptide aptamers and GO sheets.

7 In an effort to extend the peptide aptamer approach, we have developed a scaffold p

8 Using mutagenesis and a peptide aptamer approach, we pinpointed phenylalanine 79

9 Peptide aptamers are peptides constrained and presented

10 These peptide aptamers are target-specific peptides expressed

11 Here we explore the ability to use peptide aptamers as in vivo inhibitors by expressing apt

12 Here we describe the use of peptide aptamer-based affinity chromatography coupled wi

13 Our results show that peptide aptamers bear some analogies with monoclonal ant

14 Peptide aptamers, being peptide recognition moieties pre

15 t signaling, we developed three Smad-binding peptide aptamers by introducing Smad interaction motifs

16 The results suggest that Smad-binding peptide aptamers can be developed to selectively inhibit

17 Peptide aptamers can be identified that disrupt a proces

18 Specific peptide aptamers can be used in place of expensive antib

19 The peptide aptamers characterized in these studies represen

20 We report that a peptide aptamer designed to inhibit the binding between

21 A peptide aptamer DVFLGDVFLGDEC (DD) that can recognize S.

22 We expressed two peptide aptamers, each of which specifically recognizes

23 In this study, we selected 16 of the peptide aptamers for further analysis in yeast two-hybri

24 ate the use of surface-immobilized, oriented peptide aptamers for the detection of specific target pr

25 We selected peptide aptamers from combinatorial libraries that disru

26 Combined, our results demonstrate that peptide aptamers generated by yeast two-hybrid methods c

27 The thiol group from cysteine in the peptide aptamer, i.e., DD, can interact with gold ions t

28 ults of these experiments showed that all 16 peptide aptamers interact with all or most of the Rep pr

29 Here, we describe the use of Peptide Aptamer Interference (PAPTi) approach for struct

30 across potentially many thousands of arrayed peptide aptamers is predicted to simplify the production

31 Here we describe a peptide aptamer isolated from a combinatorial library th

32 antage that it can be applied for generating peptide aptamer libraries at sites within proteins witho

33 ait in a yeast two-hybrid screen of a random peptide aptamer library constrained in the active site o

34 Peptide aptamer microarrays are shown to detect low leve

35 We conclude that peptide aptamer microarrays represent a promising tool f

36 or the future creation of highly multiplexed peptide aptamer microarrays that will be compatible with

37 E6 and E7 peptide aptamer microarrays were probed with fluorescenc

38 In addition, peptide aptamer mimicking RAD51(pY315) fragment, but not

39 Forward genetic analysis with peptide aptamer "mutagens" should be particularly useful

40 employ antibodies or small molecules such as peptides, aptamers or other small molecules require that

41 ough the modification of the NP surface with peptides, aptamers, or other motifs that specifically re

42 Peptide aptamers provide probes for biological processes

43 tion of ROS-scavenging mitochondria-targeted peptide aptamer reduced genomic instability.

44 that the inactivation of protein function by peptide aptamers represents a viable approach to the und

45 e a rational approach to the design of a new peptide aptamer scaffold.

46 Peptide aptamers specific for cellular proteins included

47 rticle describes the performance of a set of peptide aptamers specific for the human papillomavirus (

48 t KD for the interaction between an oriented peptide aptamer ST(cys+)_(pep9) and the target protein C

49 , we demonstrate the high selectivity of the peptide aptamer STM_(pep9) by exposing surface-immobiliz

50 The success of peptide aptamer technology is critically dependent on th

51 Thus, we have identified a peptide aptamer that affects a function of BCL-6 that is

52 of functional screening in yeast to identify peptide aptamers that are functional in mammalian cells;

53 In an earlier study, we identified a set of peptide aptamers that bind to Rep and reduce viral repli

54 n identify bridge or connecting proteins and peptide aptamers that discriminate between closely relat

55 sed a two-bait two-hybrid system to identify peptide aptamers that distinguish allelic forms of H-Ras

56 ibe the characterization of ligand-regulated peptide aptamers that interact with and inhibit the 5'-A

57 Specifically, peptide aptamers that recognize highly related protein p

58 BCL-6 in lymphoma, we screened a library for peptide aptamers that specifically bind to BCL-6 POZ and

59 rolling the early nuclear cycles we isolated peptide aptamers that specifically bind to cyclin J and

60 ology provides a simple way to isolate small peptide aptamers that specifically recognize and strongl

61 d graphene oxide (GO) sheets with a specific peptide aptamer to create a novel, simple and label-free

62 an in vitro selection technique, to identify peptide aptamers to a protein target.

63 The use of small peptide aptamers to competitively inhibit protein intera

64 stablished the efficacy of using Rep-binding peptide aptamers to develop crops that are resistant to

65 disrupting Smad-dependent signaling using a peptide aptamer, Trx-SARA, which comprises a rigid scaff

66 These peptide aptamers were designed to mimic the recognition

67 pitope when presented in a protein, the anti-peptide aptamers were found to specifically bind to Rev.

68 Here, we report the integration of peptide aptamers with extended gate metal-oxide-semicond

69 Here we describe the isolation of peptide aptamers with optimized versions of this motif b