Biochemistry (Moscow), Supplement Series A: Membrane and Cell Biology最新文献

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Nanosystems Consisting of Iron Oxide and Serum Albumin As a Platform for Drug Delivery into Cells: Analysis of the Cy5-HSA@IONPs Nanosystem Components before and after Accumulation by Tumor Cells 由氧化铁和血清白蛋白组成的纳米系统作为药物递送到细胞的平台:Cy5-HSA@IONPs纳米系统成分在肿瘤细胞积累前后的分析
IF 1.1
Biochemistry (Moscow), Supplement Series A: Membrane and Cell Biology Pub Date : 2025-04-24 DOI: 10.1134/S1990747824700557
A. V. Toroptseva, A. A. Markova, M. T. Nguyen, M. I. Abdullina, M. V. Motyakin, O. A. Mayorova, A. V. Bychkova
{"title":"Nanosystems Consisting of Iron Oxide and Serum Albumin As a Platform for Drug Delivery into Cells: Analysis of the Cy5-HSA@IONPs Nanosystem Components before and after Accumulation by Tumor Cells","authors":"A. V. Toroptseva,&nbsp;A. A. Markova,&nbsp;M. T. Nguyen,&nbsp;M. I. Abdullina,&nbsp;M. V. Motyakin,&nbsp;O. A. Mayorova,&nbsp;A. V. Bychkova","doi":"10.1134/S1990747824700557","DOIUrl":"10.1134/S1990747824700557","url":null,"abstract":"<p>The hybrid shell@core nanosystem Cy5-HSA@IONPs containing magnetic iron oxide core and Cy5-HSA shell was engineered and characterized by composition, stability and integrity using fluorescent measurements, UV/Vis-spectrophotometry (particularly, Bradford protein assay), dynamic light scattering, electron magnetic resonance in solution, in cells and cell lysates. Conjugation of HSA to Cyanine 5 (Cy5) fluorescent dye was carried out for qualitative and quantitative estimations. The research included incubation of hybrid nanosystems with human adenocarcinoma cells (HCT116 and MCF7, colon and breast cell lines, respectively) followed by cell lysis, magnetic separation and quantitative determination of protein on the surface of the magnetic cores after mild cell lysis and in suspension of cell residues. The presence of the albumin coating on the surface of magnetic cores (IONPs) upon delivery to the cells has been proven and the effectiveness of the engineered hybrid particles as a drug (photosensitizer) delivery platform has been discussed.</p>","PeriodicalId":484,"journal":{"name":"Biochemistry (Moscow), Supplement Series A: Membrane and Cell Biology","volume":"19 1","pages":"122 - 126"},"PeriodicalIF":1.1,"publicationDate":"2025-04-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143865418","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Lysosome Functioning as a Process that Slows Down Aging 溶酶体在延缓衰老过程中的作用
IF 1.1
Biochemistry (Moscow), Supplement Series A: Membrane and Cell Biology Pub Date : 2025-04-24 DOI: 10.1134/S1990747824700387
V. A. Alekhin, S. F. Nazarova, D. R. Gizatullina, E. T. Lopatina, M. P. Kirpichnikov, M. A. Ostrovsky, V. I. Gordeliy, N. S. Ilyinsky
{"title":"Lysosome Functioning as a Process that Slows Down Aging","authors":"V. A. Alekhin,&nbsp;S. F. Nazarova,&nbsp;D. R. Gizatullina,&nbsp;E. T. Lopatina,&nbsp;M. P. Kirpichnikov,&nbsp;M. A. Ostrovsky,&nbsp;V. I. Gordeliy,&nbsp;N. S. Ilyinsky","doi":"10.1134/S1990747824700387","DOIUrl":"10.1134/S1990747824700387","url":null,"abstract":"<p>Loss of macroautophagy and loss of proteostasis are hallmarks of aging. Lysosomal dysfunction is one of the reasons for the accumulation of non-degradable defective macromolecules, protein aggregates, and damaged organelles in the cells of organisms. The summary of experimental data obtained so far indicates an age-dependent weakening of lysosomal function. We hypothesize that lysosomes, as part of the autophagy and signaling network, are of great importance for longevity. In this review, we summarize information on the mechanisms of lysosomal influence on the lifespan and existing approaches to stimulate lysosomal function for longevity. We emphasize that factors such as intraluminal pH and interactions of lysosome-associated regulatory proteins (mTOR, AMPK, TFEB, and others) are related to aging. Stimulation of lysosomal function by dietary restriction, pharmacological or optogenetic approaches could be one of the promising interventions for anti-aging protection. In particular, a novel group of lysosomal optogenetic tools with high specificity of action could be a breakthrough in aging research.</p>","PeriodicalId":484,"journal":{"name":"Biochemistry (Moscow), Supplement Series A: Membrane and Cell Biology","volume":"19 1","pages":"3 - 11"},"PeriodicalIF":1.1,"publicationDate":"2025-04-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143865379","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Searching for the Role of Mechanosensitive PIEZO1 Channel in Cell Motility and Migration of Human Aggressive Melanoma SK-MEL-2 Cells 机械敏感的PIEZO1通道在人类侵袭性黑色素瘤SK-MEL-2细胞运动和迁移中的作用
IF 1.1
Biochemistry (Moscow), Supplement Series A: Membrane and Cell Biology Pub Date : 2025-04-24 DOI: 10.1134/S1990747824700569
V. Y. Vasileva, V. I. Chubinskiy-Nadezhdin
{"title":"Searching for the Role of Mechanosensitive PIEZO1 Channel in Cell Motility and Migration of Human Aggressive Melanoma SK-MEL-2 Cells","authors":"V. Y. Vasileva,&nbsp;V. I. Chubinskiy-Nadezhdin","doi":"10.1134/S1990747824700569","DOIUrl":"10.1134/S1990747824700569","url":null,"abstract":"<p>Melanoma is one of the most common cancers in the world, especially in young adults. Due to the emergence of the resistance for treatments, the identification of novel potential molecular targets is of specific importance. Previously, we have identified functional mechanosensitive Piezo1 channels in the plasma membrane of aggressive melanoma SK-MEL-2 cell line and evidenced that selective Piezo1 activation by chemical agonist Yoda1 completely prevented melanoma spheroid formation. Here, we expanded the number of experimental tests to reveal the role of Piezo1 activity in pathophysiological reactions of SK-MEL-2 cells that are linked with cell motility and migration. In particular, we assessed the melanoma cell motility using wound closure and spheroid reactivation assay in the presence of Piezo1-selective chemical activator, Yoda1. Ca<sup>2+</sup> imaging allowed us to detect variations in a number of functionally active Piezo1 between the cells on the surface of melanoma spheroids. The processes of melanoma spheroid reactivation were unaffected by Yoda1. At the same time, wound healing assay showed a decrease of SK-MEL-2 migratory activity in the presence of Yoda1. Our results demonstrate differential roles of Piezo1 in regulation of migratory properties of melanoma cells.</p>","PeriodicalId":484,"journal":{"name":"Biochemistry (Moscow), Supplement Series A: Membrane and Cell Biology","volume":"19 1","pages":"127 - 132"},"PeriodicalIF":1.1,"publicationDate":"2025-04-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143865380","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
HSP70-NK and Target Cell Interactions: Implication to the Anticancer Effects HSP70-NK与靶细胞相互作用:对抗癌作用的影响
IF 1.1
Biochemistry (Moscow), Supplement Series A: Membrane and Cell Biology Pub Date : 2025-04-24 DOI: 10.1134/S1990747824700491
M. A. Shevchenko, O. V. Ovsyanikova, M. V. Grechikhina, D. G. Garbuz, A. A. Boyko, M. B. Evgen’ev, O. G. Zatsepina, E. I. Kovalenko, A. M. Sapozhnikov
{"title":"HSP70-NK and Target Cell Interactions: Implication to the Anticancer Effects","authors":"M. A. Shevchenko,&nbsp;O. V. Ovsyanikova,&nbsp;M. V. Grechikhina,&nbsp;D. G. Garbuz,&nbsp;A. A. Boyko,&nbsp;M. B. Evgen’ev,&nbsp;O. G. Zatsepina,&nbsp;E. I. Kovalenko,&nbsp;A. M. Sapozhnikov","doi":"10.1134/S1990747824700491","DOIUrl":"10.1134/S1990747824700491","url":null,"abstract":"<p>Heat shock protein 70 (HSP70) and HSP70-based vaccine constructs are perspective tools for anticancer therapy. One of the established anticancer effects of HSP70 is activating natural killer (NK) cells. Moreover, HSP70-activated NK cells demonstrate effectiveness in preclinical glioblastoma and lung cancer models. It is thought that the expression of HSP70 on the surface of cancer cells stimulates the cytotoxic activity of NK cells. Regarding this, the spatial aspects of NK cells with cancer cells in the presence of HSP70 are essential but not properly investigated. Using confocal laser scanning microscopy, we have recently shown that exogenously added HSP70 is absorbed on the surface of dying NK cells, while live NK cells internalize the protein. In the present study, we visualized the spatial aspects of NK cell interactions with the target breast cancer cell line BT-20 in the presence of exogenous HSP70. We traced the uptake of HSP70 by BT-20 cells and investigated NK cell behavior and contacts with BT-20 cells in the presence of HSP70. The data obtained in the present study on the interaction of BT-20 cells, NK cells, and HSP70 revealed novel aspects of HSP70-mediated anticancer efficacy of NK cells.</p>","PeriodicalId":484,"journal":{"name":"Biochemistry (Moscow), Supplement Series A: Membrane and Cell Biology","volume":"19 1","pages":"79 - 83"},"PeriodicalIF":1.1,"publicationDate":"2025-04-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143865416","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
SPR Analysis of Adrenodoxin Interaction with CYP11B1 Embedded into the Lipid Bilayer 肾上腺素还毒素与嵌入脂质双分子层的CYP11B1相互作用的SPR分析
IF 1.1
Biochemistry (Moscow), Supplement Series A: Membrane and Cell Biology Pub Date : 2025-04-24 DOI: 10.1134/S1990747824700466
O. V. Gnedenko, E. O. Yablokov, L. A. Kaluzhskiy, Y. V. Mezentsev, T. V. Tsybruk, M. A. Karpova, A. S. Ivanov
{"title":"SPR Analysis of Adrenodoxin Interaction with CYP11B1 Embedded into the Lipid Bilayer","authors":"O. V. Gnedenko,&nbsp;E. O. Yablokov,&nbsp;L. A. Kaluzhskiy,&nbsp;Y. V. Mezentsev,&nbsp;T. V. Tsybruk,&nbsp;M. A. Karpova,&nbsp;A. S. Ivanov","doi":"10.1134/S1990747824700466","DOIUrl":"10.1134/S1990747824700466","url":null,"abstract":"<p>Surface plasmon resonance (SPR) is a relevant method for studying interactions involving membrane proteins, mitochondrial proteins in particular. Currently, there is only a little information on the interaction of mitochondrial proteins with their partners, such as electron carriers, in lipid microenvironment. In this work, using cytochrome P450 11β-hydroxylase (CYP11B1) and adrenodoxin (Adx) as an example, we showed that SPR analysis can be used for studying protein–protein interactions in lipid microenvironment. Kinetic and equilibrium parameters of the CYP11B1-Adx complexes in lipid bilayers of different compositions were determined. Our results reveal that the CYP11B1-Adx complex in cardiolipin-containing bilayer demonstrates increased stability: nearly tenfold reduction in the equilibrium dissociation constant (Kd) compared to the bilayer without cardiolipin. The interaction between redox proteins is highly sensitive to the lipid structure. The immobilized protein and the lipid composition should be selected in each case, but overall, the obtained data are highly complementary for studying membrane proteins.</p>","PeriodicalId":484,"journal":{"name":"Biochemistry (Moscow), Supplement Series A: Membrane and Cell Biology","volume":"19 1","pages":"60 - 65"},"PeriodicalIF":1.1,"publicationDate":"2025-04-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143865545","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Identification of Conventional Dendritic Cell Subpopulations in Conducting Airway Mucosa 导气管粘膜常规树突状细胞亚群的鉴定
IF 1.1
Biochemistry (Moscow), Supplement Series A: Membrane and Cell Biology Pub Date : 2025-04-24 DOI: 10.1134/S1990747824700508
M. A. Shevchenko, E. A. Servuli, A. K. Kryuchkova, I. S. Okhrimenko
{"title":"Identification of Conventional Dendritic Cell Subpopulations in Conducting Airway Mucosa","authors":"M. A. Shevchenko,&nbsp;E. A. Servuli,&nbsp;A. K. Kryuchkova,&nbsp;I. S. Okhrimenko","doi":"10.1134/S1990747824700508","DOIUrl":"10.1134/S1990747824700508","url":null,"abstract":"<p>Dendritic cells belong to a heterogenic population of innate immune cells distributed across the tissues. These cells are considered to be potential therapeutic targets due to their ability to sense exogenous antigens and self-tissue damage. In the lungs, two subpopulations of conventional dendritic cells, cDC1 and cDC2, were identified. Distinguishing the populations is commonly performed by flow cytometry based on the different expressions of transcription factors and surface markers. Thus, after the exclusion of precursors and the cells rather than dendritic cells, G protein-coupled receptor XCR1 and membrane glycoprotein SIRPA (CD172a) are used to characterize cDC1 as XCR1<sup>hi</sup>CD172a<sup>lo</sup> and cDC2 as XCR1<sup>lo</sup>CD172a<sup>hi</sup>. Analysis by flow cytometry permits the accurate identification of the subpopulations; however, to define the precise location of cDC1 and cDC2 in relation to the structural tissue cells, confocal laser scanning microscopy (CLSM) is required. Together with the advantage of spatial cell distribution identification, CLSM has two limitations compared to flow cytometry. The former is the limited number of antibodies that can be simultaneously applied. Besides, not all the antibodies suitable for cell staining and flow cytometry show stable antigen recognition during the tissue staining and CLSM. In this study, we applied anti-XCR1 and anti-CD172a to visualize cDC1 and cDC2 in conducting airway mucosa of mice. We detect the distribution of these cells in a steady state and upon the airway inflammation.</p>","PeriodicalId":484,"journal":{"name":"Biochemistry (Moscow), Supplement Series A: Membrane and Cell Biology","volume":"19 1","pages":"84 - 88"},"PeriodicalIF":1.1,"publicationDate":"2025-04-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143865417","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Expression and Purification of an Archaeal Cysteine-less LOV Domain 古菌无半胱氨酸 LOV 结构域的表达与纯化
IF 1.1
Biochemistry (Moscow), Supplement Series A: Membrane and Cell Biology Pub Date : 2025-04-24 DOI: 10.1134/S199074782470048X
I. I. Natarov, O. Y. Semenov, A. A. Remeeva, I. Y. Gushchin
{"title":"Expression and Purification of an Archaeal Cysteine-less LOV Domain","authors":"I. I. Natarov,&nbsp;O. Y. Semenov,&nbsp;A. A. Remeeva,&nbsp;I. Y. Gushchin","doi":"10.1134/S199074782470048X","DOIUrl":"10.1134/S199074782470048X","url":null,"abstract":"<p>LOV (Light Oxygen Voltage) domains are ubiquitous blue light sensors widespread in all three domains of life. They mediate signal transduction in diverse biological processes and can be useful for practical applications in optogenetics and fluorescence microscopy. The canonical mechanism of LOV domains signal transduction is based on formation of the covalent adduct between flavin chromophore and the highly conserved cysteine in the active site of the protein leading to downstream signaling cascade. However, previous studies showed that there are natural cysteine-less LOV domains enabling signal transduction via flavin photoreduction. In the absence of the conserved cysteine, photoexcitation causes flavin one electron reduction to the neutral semiquinone radical state and subsequent structural reorganizations as in the canonical photocycle. In this work, previously uncharacterized natural cysteine-less LOV domain from thermophilic haloarchaeon <i>Halanaeroarchaeum sulfurireducens</i>, named <i>Hsu</i>LOV, was successfully expressed in <i>Escherichia coli</i> and purified in soluble form. Although <i>Hsu</i>LOV bound a small amount of flavin when overexpressed in <i>E. coli</i>, the chromophore load was increased by protein incubation with flavin mononucleotide in vitro. It was demonstrated that fluorescence spectra of purified and chromophore-loaded <i>Hsu</i>LOV are typical for LOV domains. Finally, the comparison of absorption spectra of dark- and light-adapted states of <i>Hsu</i>LOV revealed flavin photoreduction to the neutral semiquinone radical state, thus confirming photoactivity of <i>Hsu</i>LOV.</p>","PeriodicalId":484,"journal":{"name":"Biochemistry (Moscow), Supplement Series A: Membrane and Cell Biology","volume":"19 1","pages":"73 - 78"},"PeriodicalIF":1.1,"publicationDate":"2025-04-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143865415","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Identification of Amino Acid Residues Involved in the pH Sensitivity of Receptor Tyrosine Kinase IRR 受体酪氨酸激酶 IRR 的 pH 敏感性所涉及的氨基酸残基的鉴定
IF 1.1
Biochemistry (Moscow), Supplement Series A: Membrane and Cell Biology Pub Date : 2025-04-24 DOI: 10.1134/S1990747824700430
A. A. Gavrilenkova, D. A. Krivosheina, V. A. Pyatkina, E. V. Bocharov, I. E. Deyev
{"title":"Identification of Amino Acid Residues Involved in the pH Sensitivity of Receptor Tyrosine Kinase IRR","authors":"A. A. Gavrilenkova,&nbsp;D. A. Krivosheina,&nbsp;V. A. Pyatkina,&nbsp;E. V. Bocharov,&nbsp;I. E. Deyev","doi":"10.1134/S1990747824700430","DOIUrl":"10.1134/S1990747824700430","url":null,"abstract":"<p>IRR is a member of the insulin receptor (IR) family that has no known endogenous peptide agonists but can be activated by weak alkaline environments and has thus been proposed to function as an extracellular pH sensor. IRR activation by alkali is determined by its N-terminal extracellular region. Using recently published Cryo-EM structure of IRR ectodomain we identify three amino acids (R87, K143 and S516) that may be involved in the IRR activation by alkali. In this report we show that the triple substitution of these amino acids with alanine leads to complete disappearance of the IRR pH sensitivity. Thus, these amino acids can form one of the possible pH sensor sites in the IRR molecule.</p>","PeriodicalId":484,"journal":{"name":"Biochemistry (Moscow), Supplement Series A: Membrane and Cell Biology","volume":"19 1","pages":"41 - 45"},"PeriodicalIF":1.1,"publicationDate":"2025-04-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143865453","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Expression and Purification of Transmembrane Domain of RAGE for Structural-Dynamic NMR Studies 表达和纯化 RAGE 跨膜结构域以进行结构动态核磁共振研究
IF 1.1
Biochemistry (Moscow), Supplement Series A: Membrane and Cell Biology Pub Date : 2025-04-24 DOI: 10.1134/S1990747824700429
S. M. Dolotova, D. D. Plashchinskaia, Ya. V. Bershatsky, V. A. Lushpa, A. K. Kryuchkova, D. Zhu, I. S. Okhrimenko, E. V. Bocharov
{"title":"Expression and Purification of Transmembrane Domain of RAGE for Structural-Dynamic NMR Studies","authors":"S. M. Dolotova,&nbsp;D. D. Plashchinskaia,&nbsp;Ya. V. Bershatsky,&nbsp;V. A. Lushpa,&nbsp;A. K. Kryuchkova,&nbsp;D. Zhu,&nbsp;I. S. Okhrimenko,&nbsp;E. V. Bocharov","doi":"10.1134/S1990747824700429","DOIUrl":"10.1134/S1990747824700429","url":null,"abstract":"<p>Receptor for advanced glycation endproducts (RAGE) plays an important role in the development of inflammation and neurodegenerative diseases. There is no expression of RAGE in healthy cells, but it increases during inflammation processes that leads to tissue damage. RAGE has many ligands of different classes but with similar properties, so RAGE acts as a pattern-recognition receptor. The structure of RAGE lacks information about the transmembrane domain which is necessary for signal transduction by the receptor. In this work, for the first time, using the cell-free expression method, we obtained and purified isotope-labeled fragment of RAGE (residues 335–368, corresponding to the RAGE transmembrane domain flanked by short juxtamembrane regions). For investigation of oligomerization processes we introduced a point oncogenic mutation G349R that is located in the conservative oligomerization motif GxxxG. Nuclear magnetic resonance (NMR) studies of both peptides incorporated into dodecylphosphocholine (DPC) micelles indirectly reveal changes in protein structure and oligomerization properties following the introduction of the oncogenic G349R mutation, which is thought to affect RAGE signaling.</p>","PeriodicalId":484,"journal":{"name":"Biochemistry (Moscow), Supplement Series A: Membrane and Cell Biology","volume":"19 1","pages":"35 - 40"},"PeriodicalIF":1.1,"publicationDate":"2025-04-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143865547","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Expanding the Genetic Code in Leishmania tarentolae: A Novel Platform for Membrane Protein Expression with Unnatural Amino Acids 扩展利什曼原虫的遗传密码:用非天然氨基酸表达膜蛋白的新平台
IF 1.1
Biochemistry (Moscow), Supplement Series A: Membrane and Cell Biology Pub Date : 2025-04-24 DOI: 10.1134/S1990747824700399
I. S. Levashov, I. A. Kapranov, D. A. Kornilov, P. K. Kuzmichev, A. V. Mishin, V. I. Borshchevskiy
{"title":"Expanding the Genetic Code in Leishmania tarentolae: A Novel Platform for Membrane Protein Expression with Unnatural Amino Acids","authors":"I. S. Levashov,&nbsp;I. A. Kapranov,&nbsp;D. A. Kornilov,&nbsp;P. K. Kuzmichev,&nbsp;A. V. Mishin,&nbsp;V. I. Borshchevskiy","doi":"10.1134/S1990747824700399","DOIUrl":"10.1134/S1990747824700399","url":null,"abstract":"<p>Unnatural amino acids (UAAs) are powerful tools for investigating protein structure and dynamics. Their inclusion in a protein can help reveal important details about its functions and structural features, especially with respect to membrane proteins. However, efficient incorporation of UAAs into membrane proteins remains a challenge. In this review, we explore using <i>Leishmania tarentolae</i> (LEXSY) as a host system to express membrane proteins with incorporated UAAs, aiming to develop a versatile platform for future research and drug discovery.</p>","PeriodicalId":484,"journal":{"name":"Biochemistry (Moscow), Supplement Series A: Membrane and Cell Biology","volume":"19 1","pages":"12 - 19"},"PeriodicalIF":1.1,"publicationDate":"2025-04-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143865548","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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