ライフサイエンスコーパス: LLPS

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1 LLPS was achieved by deliquescing and then drying the pa

2 The measurements of both LLPS temperature and PEG partitioning in the ternary gam

3 These results were observed both in bulk LLPS and in lipid-stabilized, phase-separated aqueous mi

4 Importantly, while not required for LLPS, fibrillization is enhanced in protein-rich droplet

5 Consonant with the factors that induce LLPS, tau is an intrinsically disordered protein that co

6 ocal concentrations to allow for a localized LLPS driven by IDRs on RNA binding proteins.

7 the LCD of hnRNPA1 is sufficient to mediate LLPS, the RNA recognition motifs contribute to LLPS in t

8 We suggest that LCD-mediated LLPS contributes to the assembly of stress granules and

9 s show that low-complexity IDRs can modulate LLPS both positively and negatively, depending on the de

10 d domains and IDRs can cooperate to modulate LLPS, we generated a series of engineered proteins.

11 slope of the tie-lines and the dependence of LLPS temperature on polymer concentration provide a powe

12 Events of LLPS were observed for all samples with both techniques.

13 t PEG can be used to reveal the existence of LLPS for a much wider range of binary protein-water syst

14 We use our measurements of LLPS temperature as a function of protein and PEG concen

15 We show that our LLPS measurements can be also used to estimate the prote

16 We found that the wild-type IDR promotes LLPS of the polySH3-polyPRM system, decreasing the phase

17 described as liquid-liquid phase separation (LLPS) accompanied by gelation within the protein-rich ph

18 ave observed liquid-liquid phase separation (LLPS) at -8 degrees C and revealed that, in the binary g

19 s to undergo liquid-liquid phase separation (LLPS) in cells.

20 A1 undergoes liquid-liquid phase separation (LLPS) into protein-rich droplets mediated by a low compl

21 Liquid-liquid phase separation (LLPS) is thought to contribute to the establishment of m

22 (PEG) on the liquid-liquid phase separation (LLPS) of aqueous solutions of bovine gammaD-crystallin (

23 Liquid-liquid phase separation (LLPS) of RNA-binding proteins plays an important role in

24 ding-induced liquid/liquid phase separation (LLPS) on the dynamic spatial organization of FtsZ, the m

25 gests that a liquid-liquid phase separation (LLPS) process may drive their formation, possibly justif

26 ns including liquid-liquid phase separation (LLPS) while responding to changes in the ambient relativ

27 m to undergo liquid-liquid phase separation (LLPS).

28 e formed via liquid-liquid phase separation (LLPS).

29 that alter liquid-liquid phase separations (LLPS) driven by intrinsically disordered protein regions

30 on machinery, has been studied using several LLPS systems.

31 For the LLPS particles, the fRHext at each RH was between the fR

32 n X-ray microscopy (STXM) to investigate the LLPS of micrometer-sized particles undergoing a full hyd

33 Finally, we show that the increase of the LLPS temperature with PEG concentration is due to attrac

34 filaments is determined by the nature of the LLPS.

35 both the effect of PEG concentration on the LLPS temperature and proteinPEG partitioning between the

36 We furthermore show that the LLPS process is directly and sensitively tuned by salt c

37 PS, the RNA recognition motifs contribute to LLPS in the presence of RNA, giving rise to several mech

38 the concentration at which the drugs undergo LLPS in the presence of other miscible drugs, thereby re

39 cleotide repeat expansions similarly undergo LLPS and induce phase separation of a large set of prote

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