ライフサイエンスコーパス: cowpea chlorotic mottle virus

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1 psids, including poliovirus, rhinovirus, and cowpea chlorotic mottle virus.

2 ction in two related tripartite RNA viruses, cowpea chlorotic mottle virus and cucumber mosaic virus.

3 We have performed our analysis on the T = 3 cowpea chlorotic mottle virus and our estimate for the n

4 ke particles formed by the capsid protein of cowpea chlorotic mottle virus and the anionic polymer po

5 mescales of the indentation nanomechanics of Cowpea Chlorotic Mottle Virus capsid show that the capsi

6 Under large deformations, the Cowpea Chlorotic Mottle Virus capsid transitions to the

7 Models of both native and swollen cowpea chlorotic mottle virus capsids are generated from

8 We examined the in vitro assembly of the Cowpea chlorotic mottle virus (CCMV) and observed that a

9 nce, green fluorescent protein (GFP) and the cowpea chlorotic mottle virus (CCMV) are able to perform

10 n of enzymes within a single protein cage of cowpea chlorotic mottle virus (CCMV) at neutral pH.

11 the right solution conditions, for example, cowpea chlorotic mottle virus (CCMV) capsid protein (CP)

12 The N-proximal region of cowpea chlorotic mottle virus (CCMV) capsid protein (CP)

13 The comparable sequence from Cowpea Chlorotic Mottle Virus (CCMV) could also substitu

14 The mechanism by which virions of cowpea chlorotic mottle virus (CCMV) disassemble and all

15 Cowpea chlorotic mottle virus (CCMV) forms highly elasti

16 Cowpea chlorotic mottle virus (CCMV) has long been studi

17 s shown that purified capsid protein (CP) of cowpea chlorotic mottle virus (CCMV) is capable of packa

18 attraction between capsid proteins (CPs) of cowpea chlorotic mottle virus (CCMV) is controlled by th

19 Cowpea chlorotic mottle virus (CCMV) is used as a templa

20 Cowpea chlorotic mottle virus (CCMV) undergoes a well-st

21 s are then discussed with the coordinates of cowpea chlorotic mottle virus (CCMV) used to generate hy

22 bacco mosaic virus (TMV), M13 bacteriophage, cowpea chlorotic mottle virus (CCMV), and cowpea mosaic

23 hibited by VP2 virions but not by virions of cowpea chlorotic mottle virus (CCMV), another unenvelope

24 irus (TMV), Cucumber mosaic virus (CMV), and Cowpea chlorotic mottle virus (CCMV), in infections of a

25 rotein sequence identity (34% similarity) to cowpea chlorotic mottle virus (CCMV), the core structure

26 of a particularly well-studied plant virus, cowpea chlorotic mottle virus (CCMV), we demonstrate the

27 by molecular replacement using the model of cowpea chlorotic mottle virus (CCMV), which BMV closely

28 omavirus (HPV), hepatitis B virus (HBV), and cowpea chlorotic mottle virus (CCMV)-to assess both the

29 e swelling process of the icosahedral virus, cowpea chlorotic mottle virus (CCMV).

30 The elastic properties of capsids of the cowpea chlorotic mottle virus have been examined at pH 4

31 m is consistent with quantitative studies of cowpea chlorotic mottle virus, hepatitis B virus, and si

32 ckaging of RNA by the capsid protein (CP) of cowpea chlorotic mottle virus is optimal when there is a

33 AFM experiments on cowpea chlorotic mottle virus, known to undergo a pH-con

34 ene reassortant experiments with the related cowpea chlorotic mottle virus, the unfused 2a core segme

35 ased on the crystal structure of the related cowpea chlorotic mottle virus, we show that the modified

36 Here we examine the self-assembly of CP from cowpea chlorotic mottle virus with RNA molecules ranging

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