1.Homodimerization of the c-Abl protein tyrosine kinase.
Ling WEI ; Xuan LIU ; Yan-Ping YI ; Chu-Fang LI ; Yun-Long WANG ; Cheng CAO
Chinese Journal of Biotechnology 2005;21(5):698-702
The c-Abl nonreceptor tyrosine kinase is activated in the cellular responses to genotoxic, oxidative and other forms of stress. Using tagged forms of c-Abl, the present studies demonstrate that c-Abl forms homodimers in cells. The results show that the c-Abl N-terminal regions interact with the corresponding C-terminal regions of both partners in the dimmer. Specifically, the c-Abl SH3 domain binds to a proline-rich motif at amino acids 958-982 in the c-Abl C-terminal region. Deletion of the proline-rich motif disrupts dimmer formation. These findings provide the first evidence that c-Abl forms homodimers and indicate that homodimerization can contribute to the regulation of c-Abl activity.
Humans
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Protein Multimerization
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Proto-Oncogene Proteins c-abl
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genetics
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metabolism
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src Homology Domains
2.Progress and prospect in the research of bone morphogenetic protein heterodimer.
Yuanna ZHENG ; Linhong WANG ; Zhiyuan GU
Journal of Biomedical Engineering 2010;27(6):1428-1432
Bone morphogenetic protein (BMP) homodimers are of significant osteoinductivity. However, their clinical application is limited because of high effective dosage. Recently, BMP heterodimers are reported to address the issue. This is a review of the researches on BMP heterodimers, including existent evidences, types and synthetic methods, biological activities in comparison to BMP homodimers and possible mechanisms, further research direction and future expectations.
Animals
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Biopolymers
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Bone Morphogenetic Protein 2
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Bone Morphogenetic Protein 7
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Bone Morphogenetic Proteins
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genetics
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pharmacology
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Humans
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Protein Multimerization
3.Phosphatidylinositol phosphates directly bind to neurofilament light chain (NF-L) for the regulation of NF-L self assembly.
Sung Kuk KIM ; Ho KIM ; Yong Ryoul YANG ; Pann Ghill SUH ; Jong Soo CHANG
Experimental & Molecular Medicine 2011;43(3):153-160
Phosphatidylinositol phosphates (PtdInsPs) are ubiquitous membrane phospholipids that play diverse roles in cell growth and differentiation. To clarify the regulation mechanism acting on neurofilament light chain (NF-L) self assembly, we examined the effects of various PtdInsPs on this process. We found that PtdInsPs, including PI(4,5)P2, directly bind to the positively charged Arg54 of murine NF-L, and this binding promotes NF-L self assembly in vitro. Mutant NF-L (R53A/R54A) proteins lacking binding affinity to PtdInsPs did not have the same effect, but the mutant NF-L proteins showed greater self assembly than the wild-type in the absence of any PtdInsP. These results collectively suggest that Arg54 plays a pivotal role in NF-L self assembly by binding with PtdInsPs.
Animals
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Fluorescent Antibody Technique
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Mice
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Mutation/genetics
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Neurofilament Proteins/genetics/*metabolism
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Phosphatidylinositol Phosphates/*metabolism
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Phospholipase C gamma/metabolism
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*Protein Multimerization
4.Heteromerization of TRP channel subunits: extending functional diversity.
Wei CHENG ; Changsen SUN ; Jie ZHENG
Protein & Cell 2010;1(9):802-810
Transient receptor potential (TRP) channels are widely found throughout the animal kingdom. By serving as cellular sensors for a wide spectrum of physical and chemical stimuli, they play crucial physiological roles ranging from sensory transduction to cell cycle modulation. TRP channels are tetrameric protein complexes. While most TRP subunits can form functional homomeric channels, heteromerization of TRP channel subunits of either the same subfamily or different subfamilies has been widely observed. Heteromeric TRP channels exhibit many novel properties compared to their homomeric counterparts, indicating that co-assembly of TRP channel subunits has an important contribution to the diversity of TRP channel functions.
Animals
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Ankyrin Repeat
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Humans
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Models, Molecular
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Protein Interaction Domains and Motifs
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Protein Multimerization
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Protein Structure, Quaternary
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Protein Structure, Tertiary
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Protein Subunits
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TRPC Cation Channels
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chemistry
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genetics
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physiology
5.Expression, purification and interaction of human leukocyte antigen F and cluster of differentiation 8alpha homodimers.
Kaihua LUO ; Zheng FAN ; Hongbin LI ; Yiwei LIU
Chinese Journal of Biotechnology 2011;27(10):1521-1526
To obtain large quantity of human leukocyte antigen F (HLA-F) and cluster of differentiation 8alpha homodimers (CD8alphaalpha) proteins and to study their relationship, HLA-F and CD8alpha genes with rare codon in Escherichia coli were cloned using an N-terminal synonymous mutation method. High-efficiency expression protein inclusion bodies were acquired. The proteins were refolded using the dilution method and purified with gel-filtration and anion exchange chromatography. The results of gel-filtration and native-PAGE indicate that HLA-F interacts with CD8alphaalpha. This interaction may affect the binding between CD8alphaalpha and other MHC molecules to regulate immune responses. These results provide a basis for further research of HLA-F.
CD8 Antigens
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biosynthesis
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genetics
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Escherichia coli
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genetics
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metabolism
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Histocompatibility Antigens Class I
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biosynthesis
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genetics
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Humans
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Mutation
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Protein Interaction Domains and Motifs
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Protein Multimerization
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Recombinant Proteins
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biosynthesis
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genetics
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isolation & purification
6.The nucleoprotein of severe fever with thrombocytopenia syndrome virus processes a stable hexameric ring to facilitate RNA encapsidation.
Honggang ZHOU ; Yuna SUN ; Ying WANG ; Min LIU ; Chao LIU ; Wenming WANG ; Xiang LIU ; Le LI ; Fei DENG ; Hualin WANG ; Yu GUO ; Zhiyong LOU
Protein & Cell 2013;4(6):445-455
Severe fever with thrombocytopenia syndrome virus (SFTSV), a member of the Phlebovirus genus from the Bunyaviridae family endemic to China, is the causative agent of life-threatening severe fever with thrombocytopenia syndrome (SFTS), which features high fever and hemorrhage. Similar to other negative-sense RNA viruses, SFTSV encodes a nucleocapsid protein (NP) that is essential for viral replication. NP facilitates viral RNA encapsidation and is responsible for the formation of ribonucleoprotein complex. However, recent studies have indicated that NP from Phlebovirus members behaves in inhomogeneous oligomerization states. In the present study, we report the crystal structure of SFTSV NP at 2.8 Å resolution and demonstrate the mechanism by which it processes a ringshaped hexameric form to accomplish RNA encapsidation. Key residues essential for oligomerization are identified through mutational analysis and identified to have a significant impact on RNA binding, which suggests that correct formation of highly ordered oligomers is a critical step in RNA encapsidation. The findings of this work provide new insights into the discovery of new antiviral reagents for Phlebovirus infection.
Binding Sites
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Crystallography, X-Ray
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Mutation
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Nucleocapsid Proteins
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chemistry
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genetics
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metabolism
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Phlebovirus
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metabolism
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Protein Binding
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Protein Multimerization
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Protein Structure, Quaternary
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RNA, Viral
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metabolism
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Recombinant Proteins
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biosynthesis
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chemistry
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genetics
7.Preparation and identification of soluble trimeric CD40-isoleucine zipper fusion protein.
Li-Hui XU ; Yi LIU ; Xian-Hui HE
Chinese Journal of Biotechnology 2006;22(3):477-482
The interaction of CD40 with its cognate ligand, CD40L (CD154), plays important roles in immune responses. Blockade of CD40-CD40L signal pathway can protect the progression of antibody- and cell-mediated autoimmune diseases, and reduce allograft rejection thus prolonging graft survival, even engendering long-lived antigen-specific tolerance. The present study aims to enhance the binding activity of CD40 by incorporating an isoleucine zipper (IZ) trimeric motif into CD40 ectodomain to promote the formation of soluble CD40 trimers, which would be useful for blocking CD40-CD40L interaction. A prokaryotic expression vector for soluble human CD40 ectodomain fused with an IZ motif and a hexa-histidine (His6) tag at its carboxyl terminus (sCD40IZ) was constructed by multiple round PCR using cloned CD40 cDNA as a template. The recombinant sCD40IZ protein was expressed highly in Escherichia coli (E. coli) with a molecular weight of 27kD, which is consistent with its theoretical value. It mainly existed in inclusion bodies. After refolding from inclusion bodies, soluble sCD40IZ protein was purified by gel filtration. Its molecular weight in solution was about 91kD when determined by gel filtration, suggesting that it most probably existed in the form of trimers. Moreover, this protein could bind to CD40L expressed on Jurkat T cells and its binding activity was significantly higher than that of soluble CD40 without an IZ motif. These results suggest that incorporation of an IZ motif at the carboxyl terminus of soluble CD40 can facilitate the formation of trimers and enhance its binding activity with CD40L. Thus, the trimeric CD40 protein may be used to block CD40-CD40L signal pathway, suggesting that it may have potential application in preventing autoimmune diseases and transplantation rejection.
CD40 Antigens
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biosynthesis
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genetics
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metabolism
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CD40 Ligand
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metabolism
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Escherichia coli
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genetics
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metabolism
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Humans
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Isoleucine
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biosynthesis
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genetics
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Leucine Zippers
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genetics
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Protein Multimerization
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Recombinant Fusion Proteins
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biosynthesis
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genetics
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metabolism
8.Several indirect methods for analysis of CD4 self-association and its function in stable CD4-MHC-II binding.
He XIAO ; Song LI ; Bei-Fen SHEN ; Yan LI
Chinese Journal of Biotechnology 2005;21(2):239-243
To examine the self-association of CD4 molecules and preliminary studies on its biological function by several indirect methods. A series of CD4 chimeras were generated including truncated CD4 lacking the short cytoplasmic tail, deleted mutantsD1/D2 devoid of D3 and D4 and D3/D4 devoid of D1 and D2 by PCR techniques, as well as another three CD4 chimeric genes by fused human Fas cytoplasmic death domain to the downstream of the above chimeras respectively. All these molecules were subcloned into pEGFP-N1, forming the corresponding expression vectors. After introducing into HEK293 cells, gene-modified cell morphological changes and target protein subcellular localization were observed and analyzed by a confocal microscopy. Moreover, stable 293/CD4 clones were obtained by transfecting the truncated CD4 recombinant plasmid into the HEK293 cell line and selected by G418. The fluorescene intensity and rosette formation of different clones was each analyzed by a confocal microscopy and cell adhesive assays. It's seen that CD4-Fas fusion gene could induce approximately 80% cell apoptosis of transfected HEK293 cells, compared to FKBP12-Fas is about 30% and CD4 gene only is 7%. Furthermore, both D1/D2-Fas and D3/D4 Fas chimeras could trigger nearly all transfected HEK293 cells to death. Cell adhesion assays showed that neither the D1/D2 nor D3/D4 chimeras when expression in HEK293 cells binds to MHC class II + Raji B cells. Interestedly, there were two type stable clones among 293/CD4. Fluorescence intensity analysis displayed that one' mean fluorescence intensity value is about twice of the other while cell-cell binding examination showed that the former is capable of forming rosette with Raji cells but the latter. All these results suggest that CD4 molecules most likely could exist as a dimer or even an oligomer on transfected HEK293 cell surface, which constitute a functional form for stable binding to MHC class II molecules.
Antigen-Presenting Cells
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immunology
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metabolism
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CD4 Antigens
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chemistry
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genetics
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metabolism
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CD4-Positive T-Lymphocytes
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immunology
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metabolism
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Cell Line
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Dimerization
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Fas Ligand Protein
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metabolism
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Histocompatibility Antigens Class II
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genetics
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immunology
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metabolism
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Humans
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Mutagenesis, Site-Directed
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Protein Binding
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genetics
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Protein Multimerization
9.Mechanism of the Rpn13-induced activation of Uch37.
Lianying JIAO ; Songying OUYANG ; Neil SHAW ; Gaojie SONG ; Yingang FENG ; Fengfeng NIU ; Weicheng QIU ; Hongtao ZHU ; Li-Wei HUNG ; Xiaobing ZUO ; V ELEONORA SHTYKOVA ; Ping ZHU ; Yu-Hui DONG ; Ruxiang XU ; Zhi-Jie LIU
Protein & Cell 2014;5(8):616-630
Uch37 is a de-ubiquitinating enzyme that is activated by Rpn13 and involved in the proteasomal degradation of proteins. The full-length Uch37 was shown to exhibit low iso-peptidase activity and is thought to be auto-inhibited. Structural comparisons revealed that within a homo-dimer of Uch37, each of the catalytic domains was blocking the other's ubiquitin (Ub)-binding site. This blockage likely prevented Ub from entering the active site of Uch37 and might form the basis of auto-inhibition. To understand the mode of auto-inhibition clearly and shed light on the activation mechanism of Uch37 by Rpn13, we investigated the Uch37-Rpn13 complex using a combination of mutagenesis, biochemical, NMR, and small-angle X-ray scattering (SAXS) techniques. Our results also proved that Uch37 oligomerized in solution and had very low activity against the fluorogenic substrate ubiquitin-7-amino-4-methylcoumarin (Ub-AMC) of de-ubiquitinating enzymes. Uch37Δ(Hb,Hc,KEKE), a truncation removal of the C-terminal extension region (residues 256-329) converted oligomeric Uch37 into a monomeric form that exhibited iso-peptidase activity comparable to that of a truncation-containing the Uch37 catalytic domain only. We also demonstrated that Rpn13C (Rpn13 residues 270-407) could disrupt the oligomerization of Uch37 by sequestering Uch37 and forming a Uch37-Rpn13 complex. Uch37 was activated in such a complex, exhibiting 12-fold-higher activity than Uch37 alone. Time-resolved SAXS (TR-SAXS) and FRET experiments supported the proposed mode of auto-inhibition and the activation mechanism of Uch37 by Rpn13. Rpn13 activated Uch37 by forming a 1:1 stoichiometric complex in which the active site of Uch37 was accessible to Ub.
Binding Sites
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Catalytic Domain
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Chromatography, Gel
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Crystallography, X-Ray
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Humans
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Membrane Glycoproteins
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chemistry
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genetics
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metabolism
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Nuclear Magnetic Resonance, Biomolecular
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Protein Binding
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Protein Conformation
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Protein Multimerization
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Scattering, Small Angle
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Ubiquitin Thiolesterase
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chemistry
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genetics
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metabolism
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Ultracentrifugation
10.Tip-to-tip interaction in the crystal packing of PACSIN 2 is important in regulating tubulation activity.
Protein & Cell 2013;4(9):695-701
The F-BAR domain containing proteins PACSINs are cytoplasmic phosphoproteins involved in various membrane deformations, such as actin reorganization, vesicle transport and microtubule movement. Our previous study shows that all PACSINs are composed of crescent shaped dimers with two wedge loops, and the wedge loop-mediated lateral interaction between neighboring dimers is important for protein packing and tubulation activity. Here, from the crystal packing of PACSIN 2, we observed a tight tip-to-tip interaction, in addition to the wedge loop-mediated lateral interaction. With this tip-to-tip interaction, the whole packing of PACSIN 2 shows a spiral-like assembly with a central hole from the top view. Elimination of this tip-to-tip connection inhibited the tubulation function of PACSIN 2, indicating that tip-to-tip interaction plays an important role in membrane deformation activity. Together with our previous study, we proposed a packing model for the assembly of PACSIN 2 on membrane, where the proteins are connected by tip-to-tip and wedge loop-mediated lateral interactions on the surface of membrane to generate various diameter tubules.
Adaptor Proteins, Signal Transducing
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chemistry
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genetics
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Cell Membrane
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chemistry
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Crystallography, X-Ray
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Humans
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Liposomes
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chemistry
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Models, Molecular
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Mutagenesis, Site-Directed
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Protein Interaction Domains and Motifs
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Protein Multimerization
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Protein Structure, Quaternary
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Recombinant Proteins
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chemistry
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genetics
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Static Electricity