BIOCHEMISTRY-MOSCOW生物化学(莫斯科)

BIOCHEMISTRY-MOSCOW(英文缩写 BIOCHEMISTRY-MOSCOW+),ISSN 0006-2979,eISSN 1608-3040,中文译名:生物化学(莫斯科) 是一本学术期刊。本页汇总该期刊的最新影响因子、分区信息以及最新收录于 PubMed 的文献,帮助您快速了解期刊全貌。

2026 年数据 · 影响因子
2.100
JCR 分区
Q4
CAS 分区
B4
近一年发文量
155
本站 PubMed 收录统计

发文量统计区间:2025-09-27 至 2026-09-27,按本站收录文献的发表日期统计。

ISSN: 0006-2979 · eISSN: 1608-3040 · 缩写: BIOCHEMISTRY-MOSCOW+ ·中文: 生物化学(莫斯科)

期刊介绍

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期刊简介

《Biochemistry (Moscow)》是俄罗斯科学院主办的综合性生物化学期刊,发表基础与分子生物学领域的原创研究。主要涵盖蛋白质结构与功能、酶学、核酸、代谢调控、细胞信号转导及生物膜等方向。读者群为生物化学、分子生物学及相关生命科学领域的研究人员与研究生。该刊以英文出版,在国际生物化学界具有一定可见度,适合展示机制性研究成果。

研究方向

主要研究方向包括蛋白质与酶的结构功能、核酸与基因表达调控、代谢与能量转换、细胞信号转导、生物膜与运输、以及分子水平的疾病机制。论文类型以原创研究论文为主,兼有综述和短篇通讯,强调实验数据与机制探讨,也接受方法学改进和理论分析类稿件。

期刊特色

研究取向偏重分子机制与实验验证,论文通常要求较完整的生化证据链和定量分析。综述多邀请领域专家撰写,短篇通讯适合报道阶段性重要发现。适合从事基础生化、分子生物学和细胞生物学的研究者投稿,尤其适合希望在国际英文期刊展示机制性工作的作者。

投稿难度

投稿难度中等偏上,对实验设计的严谨性、数据完整性和机制深度有较高要求。建议在投稿前充分预实验、完善对照与统计,并请同行评议语言和逻辑。若工作偏描述性或机制证据不足,宜补充关键实验或改投更合适的专业期刊,不能仅凭分区判断录用难易。

历年影响因子趋势

JCR 数据年份影响因子JCR 分区
20212.824Q4
20222.800Q3
20232.300Q3
20242.200Q4
20252.100Q4

BIOCHEMISTRY-MOSCOW 最新收录文献

  1. JCR分区: Q4 CAS分区: B4 影响因子: 2.1

    1. Erratum to: Diagnostics of Synucleinopathies by Protein Amplification Methods: Methodological and Bibliometric Analysis.

    作者:
    Alexander A Groshkov, Nataliya A Kolotyeva, Pavel P Tregub, Victoria I Zhdankina, Yulia K Komleva, Alla B Salmina, Sergey N Illarioshkin
    日期:
    2026-08-01

    该文献暂无摘要。

  2. JCR分区: Q4 CAS分区: B4 影响因子: 2.1

    2. {"_":"Structural and Functional Analysis of the Recombinant Cutinase Variants for Efficient Polycaprolactone Degradation.","i":["Aureobasidium pullulans"]}

    作者:
    Filipp K Ermilov, Elena V Eneiskaya, Svetlana A Panasenko, Elena V Zhurishkina, Kirill S Bobrov, Mikhail G Petukhov, Anna A Kulminskaya, Irina A Sizova
    日期:
    2026-08-01

    Polycaprolactone (PCL) is a biodegradable polyester widely used in industry, but it degrades slowly in the environment. Enzymatic hydrolysis catalyzed by cutinases represents a promising approach for PCL waste utilization. Through screening, we selected the VKM 1116 strain capable of degrading PCL. We amplified the cutinase gene from the VKM 1116 genomic DNA. Heterologous expression in yielded ~60 mg/L of the target protein. The recombinant enzyme exhibited maximum activity at pH 6.0-6.5 and 30-40°C. Using site-directed mutagenesis, we generated single mutants (Y58W and L186F) and a double mutant (Y58W/L186F). The double mutant demonstrated the highest catalytic efficiency toward the model substrate 4-nitrophenyl 16-methylsulfonyl hexadecanoate (4-NP-(16-MS-C16)), exhibiting a two-fold increase in the hydrolysis rate compared to the wild-type enzyme. During PCL hydrolysis, the Y58W mutant showed the highest activity, providing a 1.8-fold increase in the suspension degradation rate and complete polymer granule degradation at a rate of 1 mg/h per 1 mg of protein. Our molecular modeling suggests that the hydrophobic bridge at the entrance to the active site functions as a "molecular trap." For the low-molecular-weight substrate (4-NP-(16-MS-C16)), enzymatic activity is limited by the kinetics of the substrate retention step, which is consistent with the maximum catalytic efficiency of the Y58W/L186F mutant with a closing trap. Conversely, activity toward PCL is limited by the initial adsorption stage, for which an open conformation of the free enzyme - as observed in the Y58W variant - is critically important. These results demonstrate the potential of the ApCUT1_Y58W cutinase for developing advanced PCL recycling technologies.

  3. JCR分区: Q4 CAS分区: B4 影响因子: 2.1

    3. {"_":"Effect of Cu on the Nucleoli of Cultured Astrocytes from the Rat Cerebral Cortex.","sup":["2+"]}

    作者:
    Elizaveta E Genrikhs, Elena V Stelmashook, Elena A Smirnova, Sergey A Golyshev, Alina E Lapieva, Olga P Alexandrova, Marina R Kapkaeva, Nickolay K Isaev
    日期:
    2026-08-01

    Cultured astrocytes were incubated with CuCl, which caused dose-dependent cell death (25-200 μM, 24 h). Immunocytochemical detection of the nucleolar protein nucleophosmin/B23 (NPM/B23) demonstrated that exposure to Cu (100 μM, 24 h) caused a significant increase in the surface area of NPM/B23 clusters, which was accompanied by the changes in the nucleolar ultrastructure characteristic of nucleolar stress. Longer incubation of astrocytes with Cu (100 μM, 48 h) led to accumulation of the endoplasmic reticulum (ER) stress marker GRP78, which was accompanied by the increase in nucleolar size and migration of the nucleolar material into the nucleoplasm.

  4. JCR分区: Q4 CAS分区: B4 影响因子: 2.1

    4. Dynamics of Aspartate Isomerization and Its Cellular Implications: Evidence for Isoaspartate Formation in ER-Folded Proteins and Stress-Responsive Regulation of PCMT1.

    作者:
    Burcu Biterge
    日期:
    2026-08-01

    Spontaneous isomerization of aspartate and deamidation of asparagine residues into isoaspartate (isoAsp) constitute major non-enzymatic post-translational modifications that alter protein structure, stability, and turnover. The repair enzyme protein L-isoaspartate O-methyltransferase (PCMT1) catalyzes methylation of isoAsp residues, thereby preventing their accumulation and preserving proteome integrity. Although PCMT1 has been studied extensively in cytoplasm and nucleus, its relationship to endoplasmic reticulum (ER) proteostasis remains poorly understood. Here, we investigated dynamics of aspartate isomerization within the cell, focusing on isoAsp accumulation and the regulation of PCMT1 localization under physiological and stress conditions. Using immunofluorescence, subcellular fractionation, and methylation assays, we detected isoAsp-modified proteins within the ER-enriched fractions of HeLa cells. We found that ER stress induction enhanced formation of isoAsp-containing proteins, with MG132 treatment producing the highest accumulation. PCMT1 expression increased under both stress conditions, accompanied by distinct subcellular redistribution between the cytoplasmic and nuclear compartments. These observations indicate that ER-folded proteins are susceptible to spontaneous aspartate isomerization, and that PCMT1 activity dynamically responds to proteostatic stress. Our findings provide the first experimental evidence linking isoAsp formation within the ER to PCMT1-mediated protein repair, thereby integrating chemical instability with cellular quality-control pathways. This study establishes a structural and cellular framework for understanding the dynamics of aspartate isomerization in the cell and underscores significance of PCMT1 in maintaining proteostasis under stress conditions.

  5. JCR分区: Q4 CAS分区: B4 影响因子: 2.1

    5. Experimental Models of Acute Liver Failure in Mice: From Pathogenesis and Inflammatory Cascades to the Role of Intestine.

    作者:
    Fedor A Sysonov, Ekaterina A Gorshkova, Konstantin E Menshikov, Marina S Drutskaya, Sergey A Nedospasov, Ekaterina O Gubernatorova
    日期:
    2026-08-01

    Acute liver failure (ALF) is a severe pathological condition with high mortality, arising from diverse etiologies and involving multiple pathogenetic mechanisms. ALF is often accompanied by multi-organ failure due to infectious complications. Because of disease's rapid progression, clinical studies of ALF remain limited, making the search for novel therapeutic strategies targeting specific molecular pathways and biochemical cascades a pressing task. Preclinical models are unique tools for reproducing individual aspects of ALF development. However, there is still no consensus on the gold-standard experimental animal model that fully captures ALF pathogenesis. This review systematically categorizes existing mouse models of ALF, outlining their advantages and with respect to the translational applicability of the data obtained. Among these models, we highlight the LPS/D-GalN model as the most reliable in reproducing key stages of ALF development complicated by bacterial infection. Using this model as an example, we describe the known stages of pathogenesis, supported by the experiments with pharmacologically active substances and the use of various genetically modified mouse lines. Finally, special attention is given to the intestine as an organ that sustains significant damage during ALF progression in both clinical cases and most animal models.

  6. JCR分区: Q4 CAS分区: B4 影响因子: 2.1

    6. {"_":"Age-Related Changes in -Retinoids of Lipofuscin Granules in Human Retinal Pigment Epithelium Cells.","i":["bis"]}

    作者:
    Marina A Yakovleva, Alexey A Kostyukov, Natalya L Aronshtam, Patimat M Shilkrot, Sergei A Borzenok, Vladimir A Kuzmin, Tatiana B Feldman, Aleksandr E Dontsov, Mikhail A Ostrovsky
    日期:
    2026-08-01

    Lipofuscin granules (LGs) in retinal pigment epithelium (RPE) cells contain -retinoids and their oxidation and degradation products, rendering them photo- and cytotoxic to intracellular structures. LGs are implicated in the pathogenesis of multiple visual pathologies, including age-related macular degeneration (AMD). They exhibit strong autofluorescence, which has led to the development of fundus autofluorescence (FAF) imaging as a non-invasive diagnostic method in ophthalmology. Spectral analysis of autofluorescence can expand the capabilities of this method, including for preclinical diagnostics, as pathological conditions are often associated with increased proportions of oxidized -retinoid derivatives that alter LG autofluorescence parameters. However, limited knowledge of age-dependent changes in LG -retinoid composition remains a key limitation. In this study, we combined fluorescence spectroscopy, confocal fluorescence microscopy, and fluorescence lifetime imaging (time-correlated single-photon counting) to demonstrate that, under physiological conditions, aging is accompanied by a progressive increase in the relative abundance of oxidation and degradation products of -retinoids in LGs. These findings provide an age-dependent baseline for distinguishing physiological and pathological states, thereby improving the potential of FAF imaging for early (preclinical) diagnosis.

  7. JCR分区: Q4 CAS分区: B4 影响因子: 2.1

    7. Age-Related Alterations in Retinal Monoamine Neuromodulation during AMD-Like Retinopathy Development in Rats.

    作者:
    Darya V Telegina, Alena O Kutlimetova, Arseniy E Izyurov, Alexander V Kulikov, Nataliya G Kolosova
    日期:
    2026-08-01

    Aging is the major risk factor for age-related macular degeneration (AMD), a leading cause of vision loss in aging populations. Increasing evidence suggests that alterations of neurotransmitter systems contribute to the pathogenesis of AMD. Although biogenic amines in the retina were first detected over 50 years ago, their age-related dynamics and role in AMD development are still poorly understood. Here, we compare age-related changes in the concentrations of norepinephrine, serotonin, dopamine, and their main metabolites in the retinas of senescence-accelerated OXYS rats that develop an AMD-like retinopathy and Wistar rats. We also assessed activities of monoamine oxidases (MAOs) and tyrosine hydroxylase and compared changes in these activities with transcriptome data on genes associated with biogenic amine pathways. The results revealed that in OXYS rats, retinal aging and progression of AMD-like retinopathy are primarily associated with alterations in the dopaminergic system. Specifically, dopamine and its main metabolite DOPAC were present in the retinas at higher levels than serotonin and 5-hydroxyindoleacetic acid. Furthermore, the development of retinopathy in OXYS rats was accompanied by elevated dopamine and DOPAC levels, decreased MAO activity, and changes in the expression of genes associated with the dopaminergic synapse signaling.

  8. JCR分区: Q4 CAS分区: B4 影响因子: 2.1

    8. Neuroprotective Effect of Subconjunctival Melatonin Injections in 6-Hydroxydopamine-Induced Neurotoxic Eye Damage.

    作者:
    Tatyana A Pavlenko, Natalya B Chesnokova, Olga A Lisovskaya, Olga V Beznos, Andrey V Grigoryev
    日期:
    2026-08-01

    The search for new effective methods of neuroprotection is relevant for the treatment of a wide range of common eye diseases such as age-related macular degeneration, glaucoma, and diabetic retinopathy. Using a rabbit model of neurotoxic eye damage induced by intravitreal injection of the dopaminergic neurotoxin 6-hydroxydopamine (6-OHDA), we studied the effect of subconjunctival injections of 0.1% melatonin solution on pathophysiological and biochemical processes in the eye. Administration of 6-OHDA caused destruction of the retinal pigment epithelium, narrowing of retinal vessels, hemorrhages, decrease in ocular blood flow, and intraocular pressure, as well as reduced activity of α-macroglobulin and concentrations of matrix metalloproteinase-9 and angiotensin-converting enzyme in the aqueous humor, vitreous body, and retina. Subconjunctival melatonin injections over 9 days resulted in the 2-fold on average reduction of the area of retinal damage, and normalization of the minute volume of ocular blood flow and intraocular pressure. On day 14, an increase in the α-macroglobulin activity in the aqueous humor (0.66 ± 0.19 vs. 0.49 ± 0.13 nmol/min per 1 mg protein) and vitreous body (0.50 ± 0.15 vs. 0.21 ± 0.07 nmol/min per 1 mg protein, < 0.05) was observed, along with a decrease in the matrix metalloproteinase-9 concentration (118.4 ± 34.6 vs. 524.3 ± 163.2 ng/mg, < 0.05) and angiotensin-converting enzyme concentration (371.0 ± 52.1 vs. 596.1 ± 171.5 ng/mg, < 0.05) in the retina. This indicates reduction in the intensity of inflammation and vascular wall permeability. Melatonin could be considered a promising neuroprotective component in the complex therapy of retinal diseases.

  9. JCR分区: Q4 CAS分区: B4 影响因子: 2.1

    9. EF-Hand Calcium-Binding Motif: Novel Structural and Functional Insights.

    作者:
    Konstantin A Denessiouk, Evgeny A Permyakov, Alexander I Denesyuk, Sergey E Permyakov
    日期:
    2026-08-01

    The EF-hand motif is one of the most widespread calcium-binding protein motifs in nature, mediating calcium signaling across a variety of biological processes. While structural and functional properties of the individual proteins within the EF-hand superfamily are well studied, general principles governing organization and function of these proteins are only now being elucidated. This review examines some of these emerging patterns, including recently discovered structural elements of the EF-hand motif (EF-hand zone, one-residue and three-residue units, local "Clamp" units, and "black" and "gray" clusters). Additionally, we discuss the ability of certain EF-hand proteins to recognize a broad spectrum of protein targets, as well as their zinc-binding properties. New structural data on the EF-hand domain allow proposing a structural-functional classification for the proteins in this family. Furthermore, tendency of some EF-hand proteins toward promiscuity and zinc binding significantly expands their functional importance.

  10. JCR分区: Q4 CAS分区: B4 影响因子: 2.1

    10. Photoreversible Reactions of Visual and Microbial Rhodopsins.

    作者:
    Mikhail A Ostrovsky, Olga A Smitienko, Tatiana B Feldman
    日期:
    2026-08-01

    The review discusses experimental findings and theoretical studies of photoreversible transformations of retinal-containing proteins (rhodopsins). Understanding these processes is essential for elucidating the mechanisms of photochemical and conformational transformations of these proteins. Particular emphasis is placed on visual rhodopsins, as photoreversibility plays a crucial role in its physiological regeneration in the rhabdoms of invertebrates and the cone photoreceptors of the vertebrate retina. In recent years, interest in the mechanisms of photoreversible reactions in retinal-containing proteins has grown substantially, driven by their potential applications as active components in optoelectronic devices and biosensors.

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指标接近的期刊