Acta Physico-Chimica Sinica ›› 2020, Vol. 36 ›› Issue (1): 1907053.doi: 10.3866/PKU.WHXB201907053
Special Issue: Special Issue in Honor of Academician Youqi Tang on the Occasion of His 100th Birthday
• Review • Previous Articles Next Articles
Changsheng Zhang1,*(),Luhua Lai1,2,*()
Received:
2019-07-19
Accepted:
2019-09-10
Published:
2019-09-24
Contact:
Changsheng Zhang,Luhua Lai
E-mail:changshengzhang@pku.edu.cn;lhlai@pku.edu.cn
Supported by:
Changsheng Zhang,Luhua Lai. Physiochemical Mechanisms of Biomolecular Liquid-Liquid Phase Separation[J]. Acta Physico-Chimica Sinica 2020, 36(1), 1907053. doi: 10.3866/PKU.WHXB201907053
Table 1
The model systems for experimental studying the physiochemical mechanisms of biomolecular phase separation."
No. | Description | The objective sequence | Major research results | Ref. |
a | RNA molecular with repetitive sequences | 47 x CUG,47 x CAG | CAG-repeat RNAs phase-separate in cells. With Mg2+ in solution,these two repeat sequence RNA initially phase-separate into liquid-like droplet and then rapidly become cross-linked into gels. | |
b | Nck + N-WASP | The linker L1 of Nck, between the first two SH3 domains | Mutations of L1 significantly affects the occurrence of phase separation. The concentrated distribution of positive charge residues on N-terminal, as well as the weak interactions with the second SH3 domain, are the major driving force for the L1 promoted phase separation. | |
c | (P-Xn-G)m | With different X and m value | The average hydrophobic index of X can be used to judge whether the protein has lower or upper critical solution temperature. The larger the m value, the stronger the tendency of phase separation. The sequence with upper critical solution temperature can be predicted by the parameters concluded from experiments. | |
d | VRN1 + DNA | The VRN1 linker between the B3 domains | In the model system, the linker was simulated by repetitive Pro-Ser sequences. The introduction of an alkaline residue block and/or an acidic residue block is very important for the morphology of phase separation aggregates. | |
e | PR30 + poly-rA (or poly-rU, poly-rC) | Pro-Arg repetitive sequence with homopolymeric RNA | Condensates formed with pol-rA were more viscous than those formed by poly-rC and poly-rU. The stronger interaction between arginine and adenosine makes poly-rA phase separated droplets have higher density and viscosity. Mixing RNA species generates complex multilayered condensates. | |
f | RP3/SR8 + polyU | RP3/SR8 contain RNA binding motifs RGG/RG/SR | The polyU RNA can modulate the phase behavior of the proteins. When the RNA concentration is lower, increasing the RNA concentration leads to droplet assembly by complex coacervation, and after the RNA concentration reaches to a value, increasing RNA concentration triggers a protein charge inversion, which promotes disassembly. | |
g | polyK + single/double strand nucleic acid | polyK-ss/ds RNA/DNA | PolyK with single strand nucleic acids phase separate into liquid-like droplets, and PolyK with double strand nucleic acids tends to phase separate into gel, apparently because of the difference of charge density. The phase separation morphology is also affected by ionic strength and temperature. | |
h | (PRM)n + (SH3)m | Model system for multivalent interaction | The greater the number of repeat domains, the lower the critical concentration of separation phase. The number of repeat domains also affects the tendency of droplet transition to gel state. | |
i | polyE + poly(G-K) | poly(G-K) with different charge patterns | The poly(G-K) protein with more concentrated charge pattern has an increased critical salt concentration for phase separation. Ionic entropy change is the driving force for this phase transition system. |
Table 2
Important cases of biomolecular phase separation in cell activities."
No. | Description | Scaffold molecular; assistant molecules promoting LLPS | The recruited functional client molecules | Regulation of the formation and disassembly of the aggregates | Biological functions | Ref. |
a | P granule (fertilized egg cell of elegans) | MEG-3/MEG-4 protein; RNA | Endonuclease (PGL-1 or 3), RNA helicase (GLH, LAF) | Disassemble: phosphorylation by kinase MBK-2/DYRK; assemble: dephosphorylation by phosphatase PP2A | Polarization and asymmetric division of fertilized eggs into somatic and germ cells | |
b | PGL granule (somatic cells of elegans in development) | PGL-1/PGL-3 (RGG domain; RNA, SEPA-1 | EPG-2 (promote the solidification of the droplets), Atg8 (initiate autophagic degradation) | Promotion: phosphorylation by kinase mTORC (response to high temperature); inhibition: arginine methylation by EPG11 | Autophagic degradation of PGL in somatic cells; response to high temperature | |
c | Synapsin droplets (synapses) | Synapsin 1(C terminal IDP domain) | Synaptic vesicles (DOPE lipid), SH3 domain-containing proteins (such as Grb2) | phosphorylation by kinase CaMKII results in rapidly condensates disassemble and the release of the vesicles | Control the accumulation of synaptic vesicles and their release under stimulations | |
d | Postsynaptic densities | PSD-95 (PSG domain, ligand induced dimerization) + SynGAP (Coiled-coil-PBM domain, trimer) | Disassemble: phosphorylation by kinase SynGAP | Synaptic plasticity in the nervous system, which is the mechanism of long-term potentiation/depression processes | ||
e | cGAS foci (HeLa cell) | cGAS (cyclic GMP-AMP synthase N-terminal IDP domain) + dsDNA | The substrate of cGAS: GTP,ATP | Zn2+ promotes the phase separation process | dsDNA-induced innate immune signaling | |
f | Stress granule (yeast cell, Hela cell) | Poly-A binding protein (proline-rich domain), Sup35 (prion domain) | mTORC1, DYRK3 N-terminal domain | High temperature or low pH stress drives phase separation; polyA RNA inhibits phase separation; DYRK3 regulates stress granule dissolution | Reversible protective response mechanism under stress. | |
g | Sec body (Drosophila cell, between ER and Golgi apparatus) | Sec16 | COPII coated vesicles | Mono-ADP-ribosylation of Sec16 by PARP16 promotes phase separation | Protein secretion inhibition, a protective response mechanism under environmental stress such as starvation | |
h | DNA repair compartment | 53BP1 | gH2AX + MDC1 (mediator of DNA damage checkpoint protein), tumor suppressor p53 | Protect the damaged DNA fragment; recruit repair protein for DNA damage repair | ||
i | Nuclear condensate | Nucleoprotein IDP domain, such as BRD4, TAF15 or FUS | genomic loci specifically binding with the scaffold nucleoproteins; | Restructure the genome; physically pulling in targeted genomic loci while pushing out non-targeted regions. | ||
j | Heterochromatin foci (in cell nucleus) | HP1α (dimer); DNA | chromatin | Phosphorylated HP1α forms larger and more nuclear puncta; Sgo/LBR promotes/inhibits phase separation | Gene silencing in heterochromatin | |
k | Nuclear speckle (mammalian cells) | Cyclin T1 (histidine-rich domain), DYRK1A (histidine-rich domain) | RNA polymerase Ⅱ C terminal domain, CDK9 | CDK7 or TFIIH pre-phosphorylated RNA polymerase Ⅱ promotes phase separation | C-terminal hyper-phosphorylation of RNA polymerase Ⅱ | |
l | Coactivator Puncta | MED1 (intrinsically disordered regions) | RNA polymerase Ⅱ; transcriptional coactivator: BRD4, OCT4, ER | Transcriptional regulation of the enhancer gene, bring two genomic region closer | ||
m | Splicing speckle | SRRM1 (Ser/Arg repetitive matrix protein) | Noncoding RNA, splicing factors | Phosphorylation by kinase DYRK3 promotes the condensate dissolution | Pre-mRNA splicing | |
n | Nuclear body (nucleus of Arabidopsis) | FCA+FLL2 (prion like domain) | RNA 3’-ter processing components, polyadenylation proteins: FY, FPA, and FIP1 | Reduce transcriptional read-through by promoting proximal polyadenylation at many sites | ||
o | Transport granules (neuron cell) | hnRNP A2 (low complexity domain); TDP-43 | myelin basic protein mRNA | Phosphorylation by kinase Fyn promotes the condensate dissolution and release mRNA, arginine methylation by PRMT1 inhibits phase separation | Silence the mRNA transcription and transport the mRNA molecules to translation sites | |
p | Nucleolus | GC layer: SURF6 (arginine rich domain) + NPM1 (acidic and basic tracts) | DNA/RNA, UBF, Nucleolin | Component synthesis and assembly of ribosomes | ||
q | Spindle matrix | BuGZ | α/β tubulin; Aurora A (kinase for spindle apparatus assembly regulation) | Higher temperature promotes the formation of the condensates | Regulation of assembly of the mitotic spindle apparatus | |
r | Pericentriolar material (elegans cell) | SPD-5 | α/β tubulin | Assemble: phosphorylation by kinase Polo; disassemble: dephosphorylation by phosphatase PP2A | Facilitate the nucleation and growth of microtubules | |
s | T cell microcluster 1 | LAT +Grb2 (SH2 and SH3 domain) + Sos1 | Proteins on T cell path way: CD45, ZAP70 | Assemble: tyrosine phosphorylation of LAT; disassemble: dephosphorylation by phosphatase PTP1B | Promote the signal output of the T cell signal transduction path way | |
t | T cell microcluster 2 | Nephrin + Nck (SH3 domain) + N-WASP (PRM domain) | Arp2/3 complex (nucleate actin filaments) | Promote actin aggregation into filaments | ||
u | p62 body | p62 (PB1 and UBA domains) + polyubiquitinated proteins | LC3 (receptor for selective autophagy) | Phosphorylation of p62 by kinase CK2 promotes phase separation | Drives autophagic cargo concentration and segregation | |
v | Cortial body | Sla1 + Ent1 (prion like domain) | Clathrin (adheres to cell membrane and mediates endocytosis) | Actin-independent endocytosis; droplet growth provides a driving force for cell membrane invagination |
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