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  1. Article: Experimental Investigations on the Structure of Yeast Mitochondrial Pyruvate Carriers.

    Li, Ling / Wen, Maorong / Run, Changqing / Wu, Bin / OuYang, Bo

    Membranes

    2022  Volume 12, Issue 10

    Abstract: Mitochondrial pyruvate carrier (MPC) transports pyruvate from the cytoplasm into the mitochondrial matrix to participate in the tricarboxylic acid (TCA) cycle, which further generates the energy for the physiological activities of cells. Two interacting ... ...

    Abstract Mitochondrial pyruvate carrier (MPC) transports pyruvate from the cytoplasm into the mitochondrial matrix to participate in the tricarboxylic acid (TCA) cycle, which further generates the energy for the physiological activities of cells. Two interacting subunits, MPC1 and MPC2 or MPC3, form a heterodimer to conduct transport function. However, the structural basis of how the MPC complex transports pyruvate is still lacking. Here, we described the detailed expression and purification procedures to obtain large amounts of yeast MPC1 and MPC2 for structural characterization. The purified yeast MPC1 and MPC2 were reconstituted in dodecylphosphocholine (DPC) micelles and examined using nuclear magnetic resonance (NMR) spectroscopy, showing that both subunits contain three α-helical transmembrane regions with substantial differences from what was predicted by AlphaFold2. Furthermore, the new protocol producing the recombinant MPC2 using modified maltose-binding protein (MBP) with cyanogen bromide (CNBr) cleavage introduced general way to obtain small membrane proteins. These findings provide a preliminary understanding for the structure of the MPC complex and useful guidance for further studies.
    Language English
    Publishing date 2022-09-22
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2614641-1
    ISSN 2077-0375
    ISSN 2077-0375
    DOI 10.3390/membranes12100916
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Structural characterization of a dimerization interface in the CD28 transmembrane domain.

    Wu, Hongyi / Cao, Ruiyu / Wen, Maorong / Xue, Hongjuan / OuYang, Bo

    Structure (London, England : 1993)

    2022  Volume 30, Issue 6, Page(s) 803–812.e5

    Abstract: CD28 has a crucial role in regulating immune responses by enhancing T cell activation and differentiation. Recent studies have shown that the transmembrane helix (TMH) of CD28 mediates receptor assembly and activity, but a structural characterization of ... ...

    Abstract CD28 has a crucial role in regulating immune responses by enhancing T cell activation and differentiation. Recent studies have shown that the transmembrane helix (TMH) of CD28 mediates receptor assembly and activity, but a structural characterization of TMH is still lacking. Here, we determined the dimeric helix-helix packing of CD28-TMH using nuclear magnetic resonance (NMR) technology. Unexpectedly, wild-type CD28-TMH alone forms stable tetramers in lipid bicelles instead of dimers. The NMR structure of the CD28-TMH C165F mutant reveals that a GxxxA motif, which is highly conserved in many dimeric assemblies, is located at the dimerization interface. Mutating G160 and A164 can disrupt the transmembrane helix assembly and reduces CD28 enhancement in cells. In contrast, a previously proposed YxxxxT motif does not affect the dimerization of full-length CD28, but it does affect CD28 activity. These results imply that the transmembrane domain of CD28 regulates the signaling transduction in a complicated manner.
    MeSH term(s) CD28 Antigens/genetics ; Dimerization ; Magnetic Resonance Spectroscopy ; Protein Domains ; Signal Transduction
    Chemical Substances CD28 Antigens
    Language English
    Publishing date 2022-04-08
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 1213087-4
    ISSN 1878-4186 ; 0969-2126
    ISSN (online) 1878-4186
    ISSN 0969-2126
    DOI 10.1016/j.str.2022.03.004
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Deciphering Cholesterol's Role in PD-L2 Stability: A Distinct Regulatory Mechanism From PD-L1.

    Zhang, Yu / Xiao, Taoran / Wen, Maorong / Shen, Lijuan / Du, Lingyu / Wei, Shukun / Wu, Bin / Yu, Yang / Wang, Shuqing / OuYang, Bo

    Journal of molecular biology

    2024  Volume 436, Issue 8, Page(s) 168500

    Abstract: Programmed cell death 1 ligand 2 (PD-L2), a member of the B7 immune checkpoint protein family, emerges as a crucial player in immune modulation. Despite its functional overlap with programmed cell death 1 ligand 1 (PD-L1) in binding to the programmed ... ...

    Abstract Programmed cell death 1 ligand 2 (PD-L2), a member of the B7 immune checkpoint protein family, emerges as a crucial player in immune modulation. Despite its functional overlap with programmed cell death 1 ligand 1 (PD-L1) in binding to the programmed cell death protein 1 (PD-1) on T cells, PD-L2 exhibits a divergent expression pattern and a higher affinity for PD-1. However, the regulatory mechanisms of PD-L2 remain under-explored. Here, our investigations illustrate the pivotal role of cholesterol in modulating PD-L2 stability. Using advanced nuclear magnetic resonance (NMR) and biochemical analyses, we demonstrate a direct and specific binding between cholesterol and PD-L2, mediated by an F-xxx-V-xx-LR motif in its transmembrane domain, distinct from that in PD-L1. This interaction stabilizes PD-L2 and prevents its downstream degradation. Disruption of this binding motif compromises PD-L2's cellular stability, underscoring its potential significance in cancer biology. These findings not only deepen our understanding of PD-L2 regulation in the context of tumors, but also open avenues for potential therapeutic interventions.
    MeSH term(s) B7-H1 Antigen/genetics ; B7-H1 Antigen/metabolism ; Programmed Cell Death 1 Receptor ; Protein Domains ; T-Lymphocytes/metabolism ; HEK293 Cells ; Humans ; Protein Stability ; Programmed Cell Death 1 Ligand 2 Protein/chemistry ; Programmed Cell Death 1 Ligand 2 Protein/metabolism ; Cholesterol/chemistry ; Cholesterol/metabolism
    Language English
    Publishing date 2024-02-22
    Publishing country Netherlands
    Document type Journal Article
    ZDB-ID 80229-3
    ISSN 1089-8638 ; 0022-2836
    ISSN (online) 1089-8638
    ISSN 0022-2836
    DOI 10.1016/j.jmb.2024.168500
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Expression, purification and characterization of TMCO1 for structural studies.

    Zhang, Ningning / Tang, Meng / Wen, Maorong / Cao, Yu / OuYang, Bo

    Protein expression and purification

    2020  Volume 179, Page(s) 105803

    Abstract: Transmembrane and coiled-coil domains 1 (TMCO1) has a highly conserved amino acid sequence among species, indicating a critical role of TMCO1 in cell physiology. The deficiency of TMCO1 in humans is associated with cerebrofaciothoracic dysplasia (CFTD), ... ...

    Abstract Transmembrane and coiled-coil domains 1 (TMCO1) has a highly conserved amino acid sequence among species, indicating a critical role of TMCO1 in cell physiology. The deficiency of TMCO1 in humans is associated with cerebrofaciothoracic dysplasia (CFTD), glaucoma, osteogenesis and the occurrence of cancer. TMCO1 was recently identified as an endoplasmic reticulum (ER) Ca
    MeSH term(s) Animals ; Calcium Channels/chemistry ; Calcium Channels/genetics ; Calcium Channels/isolation & purification ; Calcium Channels/metabolism ; Dictyostelium/genetics ; Escherichia coli/genetics ; Humans ; Nuclear Magnetic Resonance, Biomolecular ; Protozoan Proteins/chemistry ; Protozoan Proteins/genetics ; Protozoan Proteins/isolation & purification ; Protozoan Proteins/metabolism ; Recombinant Proteins/chemistry ; Recombinant Proteins/genetics ; Recombinant Proteins/isolation & purification ; Recombinant Proteins/metabolism ; Sf9 Cells
    Chemical Substances Calcium Channels ; Protozoan Proteins ; Recombinant Proteins ; TMCO1 protein, human
    Language English
    Publishing date 2020-11-27
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 1055455-5
    ISSN 1096-0279 ; 1046-5928
    ISSN (online) 1096-0279
    ISSN 1046-5928
    DOI 10.1016/j.pep.2020.105803
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: The nucleotide cycle of spastin correlates with its microtubule-binding properties.

    Wen, Maorong / Wang, Chunguang

    The FEBS journal

    2013  Volume 280, Issue 16, Page(s) 3868–3877

    Abstract: Spastin is an AAA (ATPase associated with diverse cellular activities) protein with microtubule (MT)-severing activity. The spastin-encoding gene was identified as the most often mutated gene in the human neurodegenerative disease hereditary spastic ... ...

    Abstract Spastin is an AAA (ATPase associated with diverse cellular activities) protein with microtubule (MT)-severing activity. The spastin-encoding gene was identified as the most often mutated gene in the human neurodegenerative disease hereditary spastic paraplegia. Although the structure of the AAA domain of spastin has been determined, the mechanism by which spastin severs MTs remains elusive. Here, we studied the MT-binding and nucleotide-binding properties of spastin, as well as their interplay. The results suggest that ATP-bound spastin interacts strongly and cooperatively with MTs; this interaction stimulates ATP hydrolysis by spastin. After ATP hydrolysis, spastin dissociates from MTs, and then exchanges ADP for ATP in solution for the next round of work. In particular, spastin in the ternary complex of MT-spastin-ATP is the most cooperative state during the working cycle, and is probably the force-generating state that is responsible for MT severing. The results presented in this study establish the nucleotide cycle of spastin in correlation with its MT-binding properties, and provide a biochemical framework for further studies of the working mechanism of spastin.
    MeSH term(s) Adenosine Diphosphate/analogs & derivatives ; Adenosine Diphosphate/metabolism ; Adenosine Triphosphatases/chemistry ; Adenosine Triphosphatases/genetics ; Adenosine Triphosphatases/metabolism ; Adenosine Triphosphate/analogs & derivatives ; Adenosine Triphosphate/metabolism ; Affinity Labels/metabolism ; Amino Acid Substitution ; Binding Sites ; Fluorescence Polarization ; Fluorescent Dyes/metabolism ; Humans ; Hydrolysis ; Kinetics ; Microtubules/metabolism ; Models, Molecular ; Mutant Proteins/chemistry ; Mutant Proteins/metabolism ; Peptide Fragments/chemistry ; Peptide Fragments/genetics ; Peptide Fragments/metabolism ; Protein Conformation ; Protein Interaction Domains and Motifs ; Recombinant Proteins/chemistry ; Recombinant Proteins/metabolism ; Solubility ; Spastin ; ortho-Aminobenzoates/metabolism
    Chemical Substances Affinity Labels ; Fluorescent Dyes ; Mutant Proteins ; Peptide Fragments ; Recombinant Proteins ; ortho-Aminobenzoates ; Adenosine Diphosphate (61D2G4IYVH) ; Adenosine Triphosphate (8L70Q75FXE) ; Adenosine Triphosphatases (EC 3.6.1.-) ; Spastin (EC 3.6.4.3) ; SPAST protein, human (EC 5.6.1.1)
    Language English
    Publishing date 2013-07-12
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2173655-8
    ISSN 1742-4658 ; 1742-464X
    ISSN (online) 1742-4658
    ISSN 1742-464X
    DOI 10.1111/febs.12385
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  6. Article: Cholesterol Binds in a Reversed Orientation to TCRβ-TM in Which Its OH Group is Localized to the Center of the Lipid Bilayer

    Wu, Hongyi / Cao, Ruiyu / Wei, Shukun / Pathan-Chhatbar, Salma / Wen, Maorong / Wu, Bin / Schamel, Wolfgang W. / Wang, Shuqing / OuYang, Bo

    Journal of molecular biology. 2021 Dec. 03, v. 433, no. 24

    2021  

    Abstract: T cell receptor (TCR) signaling in response to antigen recognition is essential for the adaptive immune response. Cholesterol keeps TCRs in the resting conformation and mediates TCR clustering by directly binding to the transmembrane domain of the TCRβ ... ...

    Abstract T cell receptor (TCR) signaling in response to antigen recognition is essential for the adaptive immune response. Cholesterol keeps TCRs in the resting conformation and mediates TCR clustering by directly binding to the transmembrane domain of the TCRβ subunit (TCRβ-TM), while cholesterol sulfate (CS) displaces cholesterol from TCRβ. However, the atomic interaction of cholesterol or CS with TCRβ remains elusive. Here, we determined the cholesterol and CS binding site of TCRβ-TM in phospholipid bilayers using solution nuclear magnetic resonance (NMR) spectroscopy and molecular dynamics (MD) simulation. Cholesterol binds to the transmembrane residues within a CARC-like cholesterol recognition motif. Surprisingly, the polar OH group of cholesterol is placed in the hydrophobic center of the lipid bilayer stabilized by its polar interaction with K154 of TCRβ-TM. An aromatic interaction with Y158 and hydrophobic interactions with V160 and L161 stabilize this reverse orientation. CS binds to the same site, explaining how it competes with cholesterol. Site-directed mutagenesis of the CARC-like motif disrupted the cholesterol/CS binding to TCRβ-TM, validating the NMR and MD results.
    Keywords T-lymphocytes ; adaptive immunity ; antigens ; cholesterol ; hydrophobicity ; lipid bilayers ; molecular biology ; molecular dynamics ; nuclear magnetic resonance spectroscopy ; phospholipids ; site-directed mutagenesis ; sulfates
    Language English
    Dates of publication 2021-1203
    Publishing place Elsevier Ltd
    Document type Article
    ZDB-ID 80229-3
    ISSN 1089-8638 ; 0022-2836
    ISSN (online) 1089-8638
    ISSN 0022-2836
    DOI 10.1016/j.jmb.2021.167328
    Database NAL-Catalogue (AGRICOLA)

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  7. Article ; Online: Regulation of PD-L1 through direct binding of cholesterol to CRAC motifs.

    Wang, Qian / Cao, Yunlei / Shen, Lijuan / Xiao, Taoran / Cao, Ruiyu / Wei, Shukun / Tang, Meng / Du, Lingyu / Wu, Hongyi / Wu, Bin / Yu, Yang / Wang, Shuqing / Wen, Maorong / OuYang, Bo

    Science advances

    2022  Volume 8, Issue 34, Page(s) eabq4722

    Abstract: Cholesterol, an essential molecule for cell structure, function, and viability, plays crucial roles in the development, progression, and survival of cancer cells. Earlier studies have shown that cholesterol-lowering drugs can inhibit the high expression ... ...

    Abstract Cholesterol, an essential molecule for cell structure, function, and viability, plays crucial roles in the development, progression, and survival of cancer cells. Earlier studies have shown that cholesterol-lowering drugs can inhibit the high expression of programmed-death ligand 1 (PD-L1) that contributes to immunoevasion in cancer cells. However, the regulatory mechanism of cell surface PD-L1 abundance by cholesterol is still controversial. Here, using nuclear magnetic resonance and biochemical techniques, we demonstrated that cholesterol can directly bind to the transmembrane domain of PD-L1 through two cholesterol-recognition amino acid consensus (CRAC) motifs, forming a sandwich-like architecture and stabilizing PD-L1 to prevent downstream degradation. Mutations at key binding residues prohibit PD-L1-cholesterol interactions, decreasing the cellular abundance of PD-L1. Our results reveal a unique regulatory mechanism that controls the stability of PD-L1 in cancer cells, providing an alternative method to overcome PD-L1-mediated immunoevasion in cancers.
    MeSH term(s) B7-H1 Antigen ; Cholesterol ; Humans ; Neoplasms
    Chemical Substances B7-H1 Antigen ; CD274 protein, human ; Cholesterol (97C5T2UQ7J)
    Language English
    Publishing date 2022-08-26
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2810933-8
    ISSN 2375-2548 ; 2375-2548
    ISSN (online) 2375-2548
    ISSN 2375-2548
    DOI 10.1126/sciadv.abq4722
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  8. Article ; Online: Expansion of KRAS hotspot mutations reactive T cells from human pancreatic tumors using autologous T cells as the antigen-presenting cells.

    Wang, Sizhen / Zhang, Xiaohui / Zou, Xuemei / Wen, Maorong / Gan, Chi / Jiang, Xiaochun / Li, Min / Shen, Rongxi / Zhu, Daojun / Yao, Anlong / Fang, Yu / Fox, Bernard A / Hu, Hong-Ming / Yu, Guangjie / Wang, Xinbo

    Cancer immunology, immunotherapy : CII

    2022  Volume 72, Issue 5, Page(s) 1301–1313

    Abstract: Adoptive cell therapy (ACT) with expanded tumor-infiltrating lymphocytes (TIL) or TCR gene-modified T cells (TCR-T) that recognize mutant KRAS neo-antigens can mediate tumor regression in patients with advanced pancreatic ductal adenocarcinoma (PDAC) ( ... ...

    Abstract Adoptive cell therapy (ACT) with expanded tumor-infiltrating lymphocytes (TIL) or TCR gene-modified T cells (TCR-T) that recognize mutant KRAS neo-antigens can mediate tumor regression in patients with advanced pancreatic ductal adenocarcinoma (PDAC) (Tran et al in N Engl J Med, 375:2255-2262, 2016; Leidner et al in N Engl J Med, 386:2112-2119, 2022). The mutant KRAS-targeted ACT holds great potential to achieve durable clinical responses for PDAC, which has had no meaningful improvement over 40 years. However, the wide application of mutant KRAS-centric ACT is currently limited by the rarity of TIL that recognize the mutant KRAS. In addition, PDAC is generally recognized as a poorly immunogenic tumor, and TILs in PDAC are less abundant than in immunogenic tumors such as melanoma. To increase the success rate of TIL production, we adopted a well-utilized K562-based artificial APC (aAPC) that expresses 4-1BBL as the costimulatory molecules to enhance the TIL production from PDCA. However, stimulation with K562-based aAPC led to a rapid loss of specificity to mutant KRAS. To selectively expand neo-antigen-specific T cells, particularly mKRAS, from the TILs, we used tandem mini gene-modified autologous T cells (TMG-T) as the novel aAPC. Using this modified IVS protocol, we successfully generated TIL cultures specifically reactive to mKRAS (G12V). We believe that autologous TMG-T cells provide a reliable source of autologous APC to expand a rare population of neoantigen-specific T cells in TILs.
    MeSH term(s) Humans ; Proto-Oncogene Proteins p21(ras)/genetics ; CD8-Positive T-Lymphocytes ; Lymphocytes, Tumor-Infiltrating ; Antigen-Presenting Cells ; Melanoma ; Pancreatic Neoplasms/genetics ; Pancreatic Neoplasms/therapy ; Mutation ; Immunotherapy, Adoptive/methods
    Chemical Substances Proto-Oncogene Proteins p21(ras) (EC 3.6.5.2) ; KRAS protein, human
    Language English
    Publishing date 2022-11-27
    Publishing country Germany
    Document type Journal Article
    ZDB-ID 195342-4
    ISSN 1432-0851 ; 0340-7004
    ISSN (online) 1432-0851
    ISSN 0340-7004
    DOI 10.1007/s00262-022-03335-w
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: PD-L1 degradation is regulated by electrostatic membrane association of its cytoplasmic domain.

    Wen, Maorong / Cao, Yunlei / Wu, Bin / Xiao, Taoran / Cao, Ruiyu / Wang, Qian / Liu, Xiwei / Xue, Hongjuan / Yu, Yang / Lin, Jialing / Xu, Chenqi / Xu, Jie / OuYang, Bo

    Nature communications

    2021  Volume 12, Issue 1, Page(s) 5106

    Abstract: The cytoplasmic domain of PD-L1 (PD-L1-CD) regulates PD-L1 degradation and stability through various mechanism, making it an attractive target for blocking PD-L1-related cancer signaling. Here, by using NMR and biochemical techniques we find that the ... ...

    Abstract The cytoplasmic domain of PD-L1 (PD-L1-CD) regulates PD-L1 degradation and stability through various mechanism, making it an attractive target for blocking PD-L1-related cancer signaling. Here, by using NMR and biochemical techniques we find that the membrane association of PD-L1-CD is mediated by electrostatic interactions between acidic phospholipids and basic residues in the N-terminal region. The absence of the acidic phospholipids and replacement of the basic residues with acidic residues abolish the membrane association. Moreover, the basic-to-acidic mutations also decrease the cellular abundance of PD-L1, implicating that the electrostatic interaction with the plasma membrane mediates the cellular levels of PD-L1. Interestingly, distinct from its reported function as an activator of AMPK in tumor cells, the type 2 diabetes drug metformin enhances the membrane dissociation of PD-L1-CD by disrupting the electrostatic interaction, thereby decreasing the cellular abundance of PD-L1. Collectively, our study reveals an unusual regulatory mechanism that controls the PD-L1 level in tumor cells, suggesting an alternative strategy to improve the efficacy of PD-L1-related immunotherapies.
    MeSH term(s) B7-H1 Antigen/chemistry ; B7-H1 Antigen/genetics ; B7-H1 Antigen/metabolism ; Cell Membrane/metabolism ; Diabetes Mellitus, Type 2 ; HEK293 Cells ; Humans ; Immunotherapy ; Membranes/metabolism ; Metformin ; Mutation ; Static Electricity
    Chemical Substances B7-H1 Antigen ; CD274 protein, human ; Metformin (9100L32L2N)
    Language English
    Publishing date 2021-08-24
    Publishing country England
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 2553671-0
    ISSN 2041-1723 ; 2041-1723
    ISSN (online) 2041-1723
    ISSN 2041-1723
    DOI 10.1038/s41467-021-25416-7
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: Cholesterol Binds in a Reversed Orientation to TCRβ-TM in Which Its OH Group is Localized to the Center of the Lipid Bilayer.

    Wu, Hongyi / Cao, Ruiyu / Wei, Shukun / Pathan-Chhatbar, Salma / Wen, Maorong / Wu, Bin / Schamel, Wolfgang W / Wang, Shuqing / OuYang, Bo

    Journal of molecular biology

    2021  Volume 433, Issue 24, Page(s) 167328

    Abstract: T cell receptor (TCR) signaling in response to antigen recognition is essential for the adaptive immune response. Cholesterol keeps TCRs in the resting conformation and mediates TCR clustering by directly binding to the transmembrane domain of the TCRβ ... ...

    Abstract T cell receptor (TCR) signaling in response to antigen recognition is essential for the adaptive immune response. Cholesterol keeps TCRs in the resting conformation and mediates TCR clustering by directly binding to the transmembrane domain of the TCRβ subunit (TCRβ-TM), while cholesterol sulfate (CS) displaces cholesterol from TCRβ. However, the atomic interaction of cholesterol or CS with TCRβ remains elusive. Here, we determined the cholesterol and CS binding site of TCRβ-TM in phospholipid bilayers using solution nuclear magnetic resonance (NMR) spectroscopy and molecular dynamics (MD) simulation. Cholesterol binds to the transmembrane residues within a CARC-like cholesterol recognition motif. Surprisingly, the polar OH group of cholesterol is placed in the hydrophobic center of the lipid bilayer stabilized by its polar interaction with K154 of TCRβ-TM. An aromatic interaction with Y158 and hydrophobic interactions with V160 and L161 stabilize this reverse orientation. CS binds to the same site, explaining how it competes with cholesterol. Site-directed mutagenesis of the CARC-like motif disrupted the cholesterol/CS binding to TCRβ-TM, validating the NMR and MD results.
    MeSH term(s) Binding Sites ; Cholesterol/chemistry ; Cholesterol Esters/chemistry ; Humans ; Hydrophobic and Hydrophilic Interactions ; Lipid Bilayers/chemistry ; Molecular Dynamics Simulation ; Mutagenesis, Site-Directed ; Nuclear Magnetic Resonance, Biomolecular ; Receptors, Antigen, T-Cell, alpha-beta/chemistry ; Receptors, Antigen, T-Cell, alpha-beta/genetics
    Chemical Substances Cholesterol Esters ; Lipid Bilayers ; Receptors, Antigen, T-Cell, alpha-beta ; Cholesterol (97C5T2UQ7J) ; cholesteryl sulfate (KU576NT9O9)
    Language English
    Publishing date 2021-10-22
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 80229-3
    ISSN 1089-8638 ; 0022-2836
    ISSN (online) 1089-8638
    ISSN 0022-2836
    DOI 10.1016/j.jmb.2021.167328
    Database MEDical Literature Analysis and Retrieval System OnLINE

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