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Influence of photobiomodulation and vitamin D on osteoblastic differentiation of human periodontal ligament stem cells and bone-like tissue formation through enzymatic activity and gene expression. 光生物调节和维生素D通过酶活性和基因表达对人牙周韧带干细胞成骨分化和骨样组织形成的影响。
Q2 Biochemistry, Genetics and Molecular Biology Pub Date : 2020-12-23 DOI: 10.1515/bmc-2020-0016
Latifa Mohamed Abdelgawad, Asmaa Mohamed Abdelaziz, Dina Sabry, Marwa Abdelgwad

Background: (1)Human periodontal ligament stem cells (HPDLSCs) are a unique population of mesenchymal stem cells (MSCs). Recently, the positive effects of photobiomodulation on the regulation of MSCs proliferation and osteogenic differentiation have gained significant attention. This study aimed to assess the effects of photobiomodulation and vitamin D (as an anabolic factor) on HPDLSCs for bone regeneration.

Methods: (2)HPDLSCs were collected, isolated, and characterized and then divided into six groups: groups I and II, control and (10-7 Mol) vitamin D, respectively; group III, irradiation at 1 J/cm2 of 808-nm diode laser; group IV, irradiation at 1 J/cm2 and culture with vitamin D; group V, irradiation at 2 J/cm2, and group VI, irradiation at 2 J/cm2 and culture with vitamin D. Cell viability assay was measured through MTT assay and cell growth curve. Alkaline phosphatase (ALP) enzyme activity and mRNA levels of RUNX2, collagen 1 (Col-1), ALP, and osteonectin were also assessed.

Results: (3)Photobiomodulation at 1 and 2 J/cm2 combined with vitamin D significantly promoted HPDLSC proliferation (in MTT assay and cell growth curve results) and osteogenic differentiation (through the gene expression of RUNX2, Col-1, ALP, and osteonectin levels (p < 0.05).

Conclusion: (4)Laser irradiation at 2 J/cm2 combined with vitamin D3 enhanced osteoblast differentiation and proliferation of cultured HPDLSCs and thus could further substitute bone grafting.

背景:(1)人牙周韧带干细胞(HPDLSCs)是一种独特的间充质干细胞(MSCs)群体。近年来,光生物调节对MSCs增殖和成骨分化的积极作用得到了广泛关注。本研究旨在评估光生物调节和维生素D(作为合成代谢因子)对HPDLSCs骨再生的影响。方法:(2)收集、分离、鉴定HPDLSCs,将其分为6组:ⅰ组和ⅱ组,分别为对照组和(10-7 Mol)维生素D组;第三组,808 nm二极管激光以1 J/cm2照射;IV组,1 J/cm2辐照,维生素D培养;V组以2j /cm2照射,VI组以2j /cm2照射并添加维生素d培养,通过MTT法和细胞生长曲线测定细胞活力。测定碱性磷酸酶(ALP)活性及RUNX2、胶原1 (Col-1)、碱性磷酸酶(ALP)、骨连接素mRNA水平。结果:(3)1、2 J/cm2光生物调节联合维生素D显著促进HPDLSC增殖(MTT试验和细胞生长曲线结果)和成骨分化(通过RUNX2、Col-1、ALP和骨连接素基因表达水平)(p < 0.05)。结论:(4)2 J/cm2激光照射联合维生素D3可增强HPDLSCs的成骨细胞分化和增殖,可进一步替代植骨。
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引用次数: 6
Mass spectrometry-based glycomic profiling of the total IgG and total proteome N-glycomes isolated from follicular fluid. 基于质谱技术对从卵泡液中分离出的总 IgG 和总蛋白质组 N-糖进行糖谱分析。
Q2 Biochemistry, Genetics and Molecular Biology Pub Date : 2020-10-25 DOI: 10.1515/bmc-2020-0015
Marko Klobučar, Sanja Dević Pavlić, Iris Car, Neda Smiljan Severinski, Tamara Tramišak Milaković, Anđelka Radojčić Badovinac, Sandra Kraljević Pavelić

Couples with infertility issues have been assisted by in vitro fertilization reproduction technologies with high success rates of 50-80%. However, complications associated with ovarian stimulation remain, such as ovarian hyperstimulation. Oocyte quality is a significant factor impacting the outcome of in vitro fertilization procedures, but other processes are also critical for fertilization success. Increasing evidence points to aberrant inflammation as one of these critical processes reflected in molecular changes, including glycosylation of proteins. Here we report results from a MALDI-TOF-MS-based glycomic profiling of the total IgG and total proteome N-glycomes isolated from the follicular fluid obtained from patients undergoing fertilization through either (1) assisted reproduction by modified natural cycle or (2) controlled ovarian stimulation (GnRH antagonist, GnRH Ant) protocols. Significant inflammatory-related differences between analyzed N-glycomes were observed from samples and correlated with the ovarian stimulation protocol used in patients.

体外受精生殖技术为有不孕问题的夫妇提供了帮助,成功率高达 50-80%。然而,与卵巢刺激相关的并发症依然存在,如卵巢过度刺激。卵母细胞质量是影响体外受精过程结果的重要因素,但其他过程对受精成功也至关重要。越来越多的证据表明,异常炎症是这些关键过程之一,反映在分子变化上,包括蛋白质的糖基化。在此,我们报告了一项基于 MALDI-TOF-MS 的糖基化分析结果,该分析从通过(1)改良自然周期辅助生殖或(2)受控卵巢刺激(GnRH 拮抗剂,GnRH Ant)方案进行受精的患者卵泡液中分离出的总 IgG 和总蛋白质组 N-糖基化物。从样本中观察到分析的 N-苷元之间存在明显的炎症相关差异,并与患者使用的卵巢刺激方案相关。
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引用次数: 0
A Novel Conceptual Model for the Dual Role of FOF1-ATP Synthase in Cell Life and Cell Death. FOF1-ATP 合成酶在细胞生命和细胞死亡中双重作用的新概念模型。
Q2 Biochemistry, Genetics and Molecular Biology Pub Date : 2020-08-22 DOI: 10.1515/bmc-2020-0014
Sunil Nath

The mitochondrial permeability transition (MPT) has been one of the longstanding enigmas in biology. Its cause is currently at the center of an extensive scientific debate, and several hypotheses on its molecular nature have been put forward. The present view holds that the transition arises from the opening of a high-conductance channel in the energy-transducing membrane, the permeability transition pore (PTP), also called the mitochondrial megachannel or the multiconductance channel (MMC). Here, the novel hypothesis is proposed that the aqueous access channels at the interface of the c-ring and the a-subunit of FO in the FOF1-ATP synthase are repurposed during induction of apoptosis and constitute the elusive PTP/ MMC. A unifying principle based on regulation by local potentials is advanced to rationalize the action of the myriad structurally and chemically diverse inducers and inhibitors of PTP/MMC. Experimental evidence in favor of the hypothesis and its differences from current models of PTP/MMC are summarized. The hypothesis explains in considerable detail how the binding of Ca2+ to a β-catalytic site (site 3) in the F1 portion of ATP synthase triggers the opening of the PTP/MMC. It is also shown to connect to longstanding proposals within Nath's torsional mechanism of energy transduction and ATP synthesis as to how the binding of MgADP to site 3 does not induce PTP/MMC, but instead catalyzes physiological ATP synthesis in cell life. In the author's knowledge, this is the first model that explains how Ca2+ transforms the FOF1-ATP synthase from an exquisite energy-conserving enzyme in cell life into an energy-dissipating structure that promotes cell death. This has major implications for basic as well as for clinical research, such as for the development of drugs that target the MPT, given the established role of PTP/MMC dysregulation in cancer, ischemia, cardiac hypertrophy, and various neurodegenerative diseases.

线粒体通透性转换(MPT)一直是生物学中长期存在的谜团之一。其原因目前正处于科学界广泛争论的焦点,人们对其分子性质提出了多种假说。目前的观点认为,这种转变是由于能量转换膜上的一个高导通道--通透性转换孔(PTP)(也称线粒体巨通道或多导通道(MMC))--打开所致。本文提出了一个新的假设,即在诱导细胞凋亡的过程中,FOF1-ATP 合酶中的 c 环和 FO 的 a 亚基界面上的水接入通道被重新利用,并构成了难以捉摸的 PTP/ MMC。该研究提出了一个基于局部电位调节的统一原理,以合理解释 PTP/MMC 无数结构和化学上不同的诱导剂和抑制剂的作用。本文总结了支持该假说的实验证据及其与当前 PTP/MMC 模型的不同之处。该假说相当详细地解释了 Ca2+ 与 ATP 合成酶 F1 部分的一个 β 催化位点(位点 3)结合是如何触发 PTP/MMC 打开的。研究还表明,这与 Nath 的能量转移和 ATP 合成的扭转机制中长期提出的建议有关,即 MgADP 与位点 3 结合不会诱导 PTP/MMC,而是会催化细胞生命中的生理性 ATP 合成。据作者所知,这是第一个解释 Ca2+ 如何将 FOF1-ATP 合成酶从细胞生命中的精致能量守恒酶转变为促进细胞死亡的能量耗散结构的模型。鉴于 PTP/MMC 失调在癌症、缺血、心肌肥厚和各种神经退行性疾病中的作用已得到证实,这对基础研究和临床研究都有重大意义,例如开发针对 MPT 的药物。
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引用次数: 0
Insights into Endothelin-3 and Multiple Sclerosis. 对内皮素-3 和多发性硬化症的认识
Q2 Biochemistry, Genetics and Molecular Biology Pub Date : 2020-06-25 DOI: 10.1515/bmc-2020-0012
Lucia Monti, Umberto Arrigucci, Alessandro Rossi

Endothelins are powerful vasoconstrictor peptides that play numerous other roles. Endothelin-1 (ET1) is the principal isoform produced by the endothelium in the human cardiovascular system. Endothelin-3 (ET3) and its rPptor affinity have been demonstrated to support neuronal repair mechanisms throughout life. In multiple sclerosis (MS), the role of vasoactive peptides are not well defined. Here we focus on ET3, specifically the plasma levels between MS patients and healthy subjects. Furthermore, we evaluated the changes in ET1 and ET3 plasma levels during different disease phases, the correlation between ET3 and cerebral circulation time, and the relationship between ET1 and ET3. In MS patients, the ET3 plasma levels were altered in a time-dependent manner. These results could support a putative role of ET3 in neuroprotection and/or neuroimmune modulation over time.

内皮素是一种强有力的血管收缩肽,还能发挥许多其他作用。内皮素-1(ET1)是人体心血管系统内皮细胞产生的主要同工酶。内皮素-3(ET3)及其 rPptor 亲和力已被证实在整个生命过程中支持神经元修复机制。在多发性硬化症(MS)中,血管活性肽的作用尚未明确。在此,我们重点研究了 ET3,特别是多发性硬化症患者与健康人之间的血浆水平。此外,我们还评估了不同疾病阶段 ET1 和 ET3 血浆水平的变化、ET3 与脑循环时间的相关性以及 ET1 和 ET3 之间的关系。在多发性硬化症患者中,ET3血浆水平的变化与时间有关。这些结果支持了 ET3 在神经保护和/或神经免疫调节中的假定作用。
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引用次数: 0
Erratum to "Polymorphism of MMP1 and MMP3 promoter regions and HR-HPV infection in women from Burkina Faso and Côte d'Ivoire". 对“MMP1和MMP3启动子区域多态性与布基纳法索和Côte科特迪瓦妇女HR-HPV感染”的勘误。
Q2 Biochemistry, Genetics and Molecular Biology Pub Date : 2020-06-20 DOI: 10.1515/bmc-2020-0013
Prosper Bado, Florencia Wendkuuni Djigma, Théodora Mahoukèdè Zohoncon, Dorcas Obiri-Yeboah, Esther Mah Alima Traoré, Abdoul Karim Ouattara, Teega-Wendé Clarisse Ouedraogo, Shoukrat Ohuwa Toyin Bello, Marius Ayaovi Setor, Ina Marie Angèle Traore, Apollinaire Horo, Kouame Privat Kouakou, Théophane Albert Yonli, Charlemagne Ouedraogo, Jacques Simpore
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引用次数: 1
Genotypic distribution of human oncogenic papillomaviruses in sexually active women in Burkina Faso: Central, Central-Eastern and Hauts-Bassins regions. 布基纳法索性活跃妇女中人类致癌乳头瘤病毒的基因型分布:中部、中东部和上盆地地区。
Q2 Biochemistry, Genetics and Molecular Biology Pub Date : 2020-05-17 DOI: 10.1515/bmc-2020-0011
Rogomenoma Alice Ouedraogo, Théodora Mahoukèdè Zohoncon, Ina Marie Angèle Traore, Abdoul Karim Ouattara, Sindimalgdé Patricia Guigma, Florencia Wendkuuni Djigma, Dorcas Obiri-Yeboah, Charlemagne Ouedraogo, Jacques Simpore

Objective this study was conducted to determine the distribution of high-risk human papillomavirus (HR-HPV) genotypes in women in the general population of three regions of Burkina Faso. Method This multicenter, descriptive cross-sectional study involved 1321 sexually active women in five cities in three regions of Burkina Faso: Central, Central-Eastern and Hauts-Bassins regions. After collection of endocervical specimens, pre-cervical lesions were screened by visual inspection with acetic acid and lugol (VIA / VILI). HR-HPV genotypes were characterized by multiplex real-time PCR after extraction of viral DNA. Results The mean age of women was 31.98 ± 10.09 years. The HR-HPV infection in the three regions ranged from 26.16% to 43.26% with 35.42% as overall prevalence in women. The most common HR-HPV genotypes in descending order were: HPV 56, 52, 66, 59, 39, 51, 18, 35. The prevalence of bivalent vaccine genotypes (HPV16 / 18) was 7.83% against 63.78% of genotypes not covered by HPV vaccine; 36.32% (170/468) of women had multiple concomitant HR-HPV infections. Conclusion this study showed significant regional variation and high prevalence of HR-HPV infection in women. The predominant genotypes differ from those covered by available vaccines in Burkina Faso. These results will help guide our health policies towards better prevention of cervical cancer. The diversity of oncogenic genotypes is sparking a large-scale study in the West African sub-region, particularly in cases of cancer and the introduction of the nonavalent vaccine which includes HPV 52 found among the predominant genotypes in this study.

目的 本研究旨在确定布基纳法索三个地区普通人群中女性高危人乳头瘤病毒(HR-HPV)基因型的分布情况。方法 这项多中心、描述性横断面研究涉及布基纳法索三个地区五个城市的 1321 名性活跃妇女:中央区、中东部区和上盆地区。在收集宫颈内膜标本后,通过醋酸和鲁戈尔(VIA/VILI)肉眼检查法筛查宫颈前病变。提取病毒 DNA 后,通过多重实时 PCR 鉴定 HR-HPV 基因型。结果 妇女的平均年龄为(31.98 ± 10.09)岁。三个地区的 HR-HPV 感染率从 26.16% 到 43.26% 不等,女性总感染率为 35.42%。最常见的 HR-HPV 基因型从高到低依次为HPV 56、52、66、59、39、51、18、35。二价疫苗基因型(HPV16/18)的流行率为 7.83%,而 HPV 疫苗未涵盖的基因型的流行率为 63.78%;36.32% 的妇女(170/468)同时患有多种 HR-HPV 感染。结论:本研究表明,妇女中的 HR-HPV 感染存在明显的地区差异和高流行率。主要基因型与布基纳法索现有疫苗所覆盖的基因型不同。这些结果将有助于指导我们的卫生政策,更好地预防宫颈癌。致癌基因型的多样性引发了西非次区域的大规模研究,特别是在癌症病例和引入无价疫苗方面,其中包括本研究中发现的主要基因型中的 HPV 52。
{"title":"Genotypic distribution of human oncogenic papillomaviruses in sexually active women in Burkina Faso: Central, Central-Eastern and Hauts-Bassins regions.","authors":"Rogomenoma Alice Ouedraogo, Théodora Mahoukèdè Zohoncon, Ina Marie Angèle Traore, Abdoul Karim Ouattara, Sindimalgdé Patricia Guigma, Florencia Wendkuuni Djigma, Dorcas Obiri-Yeboah, Charlemagne Ouedraogo, Jacques Simpore","doi":"10.1515/bmc-2020-0011","DOIUrl":"10.1515/bmc-2020-0011","url":null,"abstract":"<p><p>Objective this study was conducted to determine the distribution of high-risk human papillomavirus (HR-HPV) genotypes in women in the general population of three regions of Burkina Faso. Method This multicenter, descriptive cross-sectional study involved 1321 sexually active women in five cities in three regions of Burkina Faso: Central, Central-Eastern and Hauts-Bassins regions. After collection of endocervical specimens, pre-cervical lesions were screened by visual inspection with acetic acid and lugol (VIA / VILI). HR-HPV genotypes were characterized by multiplex real-time PCR after extraction of viral DNA. Results The mean age of women was 31.98 ± 10.09 years. The HR-HPV infection in the three regions ranged from 26.16% to 43.26% with 35.42% as overall prevalence in women. The most common HR-HPV genotypes in descending order were: HPV 56, 52, 66, 59, 39, 51, 18, 35. The prevalence of bivalent vaccine genotypes (HPV16 / 18) was 7.83% against 63.78% of genotypes not covered by HPV vaccine; 36.32% (170/468) of women had multiple concomitant HR-HPV infections. Conclusion this study showed significant regional variation and high prevalence of HR-HPV infection in women. The predominant genotypes differ from those covered by available vaccines in Burkina Faso. These results will help guide our health policies towards better prevention of cervical cancer. The diversity of oncogenic genotypes is sparking a large-scale study in the West African sub-region, particularly in cases of cancer and the introduction of the nonavalent vaccine which includes HPV 52 found among the predominant genotypes in this study.</p>","PeriodicalId":38392,"journal":{"name":"Biomolecular Concepts","volume":"11 1","pages":"125-136"},"PeriodicalIF":0.0,"publicationDate":"2020-05-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10014875","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
Polymorphism of MMP1 and MMP3 promoter regions and HR-HPV infection in women from Burkina Faso and Côte d'Ivoire. 布基纳法索和科特迪瓦妇女 MMP1 和 MMP3 启动子区域的多态性与 HR-HPV 感染。
Q2 Biochemistry, Genetics and Molecular Biology Pub Date : 2020-05-17 DOI: 10.1515/bmc-2020-0010
Prosper Bado, Florencia Djigma Wendkuuni, Mahoukèdè Zohoncon Théodora, Dorcas Obiri-Yeboah, Alima Traoré Esther Mah, Karim Ouattara Abdoul, Clarisse Ouedraogo Teega-Wendé, Toyin Bello Shoukrat Ohuwa, Ayaovi Setor Marius, Angèle Traore Ina Marie, Apollinaire Horo, Privat Kouakou Kouame, Théophane Yonli Albert, Charlemagne Ouedraogo, Jacques Simpore

The single nucleotide polymorphism (SNP) of the promoter region of MMP-1 (at 1607 bp) and MMP-3 (at 1171 bp) create Ets binding sites. Correlations between these SNPs and sensitivity to several biological processes such as metastasis and recurrence of cancer have been reported in several studies. In this case-control study, we looked for these SNPs in women infected with or not with high-risk human papillomaviruses (HR-HPV). The frequency, distribution and correlation of these SNPs with the presence or absence of HR-HPV infection were evaluated. Genotypes 1G1G, 1G2G and 2G2G for MMP1 and genotypes 5A5A, 5A6A, 6A6A for MMP3 were found in our study population. In general, we noted that the 1G (40.8%) and 2G (64.8%) alleles were more frequent in non-infected women and infected women, respectively, and more specifically this difference was significant in women from Côte d'Ivoire. These results, although yet to be reaffirmed with assays for quantifying the mRNA of these genes, suggest that the SNP of the MMP-1 promoter could promote infection with HR-HPV.

MMP-1(1607 bp处)和MMP-3(1171 bp处)启动子区域的单核苷酸多态性(SNP)产生了Ets结合位点。已有多项研究报道了这些 SNP 与癌症转移和复发等多个生物学过程的敏感性之间的相关性。在这项病例对照研究中,我们在感染或未感染高危人乳头瘤病毒(HR-HPV)的妇女中寻找这些 SNPs。我们评估了这些 SNPs 的频率、分布以及与是否感染 HR-HPV 的相关性。在我们的研究人群中发现了 MMP1 的基因型 1G1G、1G2G 和 2G2G,以及 MMP3 的基因型 5A5A、5A6A 和 6A6A。总的来说,我们注意到 1G(40.8%)和 2G(64.8%)等位基因分别在非感染妇女和感染妇女中更为常见,更具体地说,这种差异在科特迪瓦妇女中非常明显。尽管这些结果还有待于通过对这些基因的 mRNA 进行定量检测来再次证实,但这些结果表明,MMP-1 启动子的 SNP 可能会促进感染 HR-HPV。
{"title":"Polymorphism of MMP1 and MMP3 promoter regions and HR-HPV infection in women from Burkina Faso and Côte d'Ivoire.","authors":"Prosper Bado, Florencia Djigma Wendkuuni, Mahoukèdè Zohoncon Théodora, Dorcas Obiri-Yeboah, Alima Traoré Esther Mah, Karim Ouattara Abdoul, Clarisse Ouedraogo Teega-Wendé, Toyin Bello Shoukrat Ohuwa, Ayaovi Setor Marius, Angèle Traore Ina Marie, Apollinaire Horo, Privat Kouakou Kouame, Théophane Yonli Albert, Charlemagne Ouedraogo, Jacques Simpore","doi":"10.1515/bmc-2020-0010","DOIUrl":"10.1515/bmc-2020-0010","url":null,"abstract":"<p><p>The single nucleotide polymorphism (SNP) of the promoter region of MMP-1 (at 1607 bp) and MMP-3 (at 1171 bp) create Ets binding sites. Correlations between these SNPs and sensitivity to several biological processes such as metastasis and recurrence of cancer have been reported in several studies. In this case-control study, we looked for these SNPs in women infected with or not with high-risk human papillomaviruses (HR-HPV). The frequency, distribution and correlation of these SNPs with the presence or absence of HR-HPV infection were evaluated. Genotypes 1G1G, 1G2G and 2G2G for MMP1 and genotypes 5A5A, 5A6A, 6A6A for MMP3 were found in our study population. In general, we noted that the 1G (40.8%) and 2G (64.8%) alleles were more frequent in non-infected women and infected women, respectively, and more specifically this difference was significant in women from Côte d'Ivoire. These results, although yet to be reaffirmed with assays for quantifying the mRNA of these genes, suggest that the SNP of the MMP-1 promoter could promote infection with HR-HPV.</p>","PeriodicalId":38392,"journal":{"name":"Biomolecular Concepts","volume":"11 1","pages":"116-124"},"PeriodicalIF":0.0,"publicationDate":"2020-05-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10006054","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
Three-dimensional reconstruction of individual helical nano-filament structures from atomic force microscopy topographs. 从原子力显微镜拓扑图三维重建单个螺旋纳米丝结构。
Q2 Biochemistry, Genetics and Molecular Biology Pub Date : 2020-05-06 DOI: 10.1515/bmc-2020-0009
Liisa Lutter, Christopher J Serpell, Mick F Tuite, Louise C Serpell, Wei-Feng Xue

Atomic force microscopy, AFM, is a powerful tool that can produce detailed topographical images of individual nano-structures with a high signal-to-noise ratio without the need for ensemble averaging. However, the application of AFM in structural biology has been hampered by the tip-sample convolution effect, which distorts images of nano-structures, particularly those that are of similar dimensions to the cantilever probe tips used in AFM. Here we show that the tip-sample convolution results in a feature-dependent and non-uniform distribution of image resolution on AFM topographs. We show how this effect can be utilised in structural studies of nano-sized upward convex objects such as spherical or filamentous molecular assemblies deposited on a flat surface, because it causes 'magnification' of such objects in AFM topographs. Subsequently, this enhancement effect is harnessed through contact-point based deconvolution of AFM topographs. Here, the application of this approach is demonstrated through the 3D reconstruction of the surface envelope of individual helical amyloid filaments without the need of cross-particle averaging using the contact-deconvoluted AFM topographs. Resolving the structural variations of individual macromolecular assemblies within inherently heterogeneous populations is paramount for mechanistic understanding of many biological phenomena such as amyloid toxicity and prion strains. The approach presented here will also facilitate the use of AFM for high-resolution structural studies and integrative structural biology analysis of single molecular assemblies.

原子力显微镜(AFM)是一种功能强大的工具,可生成单个纳米结构的详细地形图像,信噪比高,无需进行集合平均。然而,原子力显微镜在结构生物学中的应用一直受到针尖-样品卷积效应的阻碍,这种效应会扭曲纳米结构的图像,尤其是那些与原子力显微镜使用的悬臂探针针尖尺寸相似的纳米结构。在这里,我们展示了针尖-样本卷积会导致原子力显微镜拓扑图上的图像分辨率出现依赖于特征的非均匀分布。我们展示了如何将这种效应用于纳米级上凸物体(如沉积在平面上的球形或丝状分子组装体)的结构研究,因为它会导致这类物体在原子力显微镜地形图上 "放大"。随后,通过对原子力显微镜拓扑图进行基于接触点的解卷积,利用这种增强效应。在此,我们通过使用接触解卷积 AFM 拓扑图对单个螺旋淀粉样蛋白丝的表面包络进行三维重建,而无需进行跨粒子平均,从而展示了这种方法的应用。要从机理上理解淀粉样蛋白毒性和朊病毒菌株等许多生物现象,最重要的是解决固有异质群体中单个大分子组装体的结构变化问题。本文介绍的方法还将有助于利用原子力显微镜对单个分子组装体进行高分辨率结构研究和综合结构生物学分析。
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引用次数: 0
Chemical composition, antioxidant, anti-inflammatory and antiproliferative activities of the essential oil of Cymbopogon nardus, a plant used in traditional medicine. 传统医学中使用的一种植物--纳豆香茅(Cymbopogon nardus)精油的化学成分、抗氧化、抗炎和抗增殖活性。
Q2 Biochemistry, Genetics and Molecular Biology Pub Date : 2020-04-15 DOI: 10.1515/bmc-2020-0007
Bagora Bayala, Ahmed Y Coulibaly, Florencia W Djigma, Bolni Marius Nagalo, Silvère Baron, Gilles Figueredo, Jean-Marc A Lobaccaro, Jacques Simpore

Objectives Natural products commonly used in traditional medicine, such as essential oils (EOs), are attractive sources for the development of molecules with anti-proliferative activities for future treatment of human cancers, e.g., prostate and cervical cancer. In this study, the chemical composition of the EO from Cymbopogon nardus was characterized, as well as its antioxidativeproperties and anti-inflammatory and antiproliferative activities on LNCaP cells derived from prostate cancer. Methods The chemical composition of the EO was determined by GC/FID and GC/MS analyses. The antioxidative properties were assessed using DPPH radical scavenging assay and ABTS+• radical cation decolorization assay, and the anti-inflammatory capacity was determined by the inhibition of the lipoxygenase activity. Antiproliferative activity was evaluated by MTT assay. Results Collectively, our data show that the major constituents of C. nardus EO are citronellal (33.06 %), geraniol (28.40 %), nerol (10.94 %), elemol (5.25 %) and delta-elemene (4.09 %). C. nardus EO shows modest antioxidant and anti-inflammatory activity compared to the standard galic acid. C. nardus EO exhibits the best antiproliferative activity on the prostate cancer cell line LNCaP with an IC50 of 58.0 ± 7.9 μg/mL, acting through the induction of the cell cycle arrest. Conclusions This study has determined that C. nardus EO efficiently triggers cytotoxicity and pens a new field of investigation regarding the putative use of this EO in vivo.

目的 传统医学中常用的天然产品,如精油(EOs),是开发具有抗增殖活性的分子以用于未来治疗人类癌症(如前列腺癌和宫颈癌)的有吸引力的来源。在这项研究中,研究人员对从香叶中提取的香叶油的化学成分、抗氧化性、抗炎和抗前列腺癌 LNCaP 细胞增殖活性进行了表征。方法 通过 GC/FID 和 GC/MS 分析确定酢浆草的化学成分。采用 DPPH 自由基清除试验和 ABTS+-自由基阳离子脱色试验评估其抗氧化性,并通过抑制脂氧合酶活性来确定其抗炎能力。抗增殖活性通过 MTT 试验进行评估。研究结果表明,纳豆油的主要成分为香茅醛(33.06%)、香叶醇(28.40%)、橙花醇(10.94%)、香叶醇(5.25%)和δ-榄香烯(4.09%)。与标准半乳糖酸相比,纳豆油显示出适度的抗氧化和抗炎活性。纳豆油对前列腺癌细胞株 LNCaP 的抗增殖活性最佳,IC50 为 58.0 ± 7.9 μg/mL,通过诱导细胞周期停滞发挥作用。结论 本研究确定了纳豆环氧乙烷可有效引发细胞毒性,并为该环氧乙烷在体内的潜在用途开辟了一个新的研究领域。
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引用次数: 0
Association of TNF-α-308G/A and IL-18 Polymorphisms with risk of HPV infection among sexually active women in Burkina Faso. TNF-α-308G/A 和 IL-18 多态性与布基纳法索性活跃妇女感染 HPV 风险的关系。
Q2 Biochemistry, Genetics and Molecular Biology Pub Date : 2020-04-15 DOI: 10.1515/bmc-2020-0008
Ina M A Traore, Théodora M Zohoncon, Florencia W Djigma, T Rebeca Compaore, Yves Traore, Jacques Simpore

Human papillomavirus (HPV) infection is the most common sexually transmitted infection worldwide. Persistence infection can lead to the development of cervical cancer potentially due to some genetic factors such as polymorphisms in regulatory and coding regions of cytokine genes. The purpose of this study was to determine whether there is a relationship between TNF-308 G/A or IL18 polymorphisms and high-risk HPV infection among sexually active women from Burkina Faso. Ninety-one HPV infected and two hundred and nine HPV negative women (the latter used as healthy controls) were screened. TNFA-308 G/A and IL18-607 C/A polymorphisms were detected using the TaqMan allelic discrimination. HPV 52 (21.19%), HPV 39 (11.86%) and HPV 33 (11.02%) were the most common HPV genotypes. The TNFA-308A and IL18-607 C alleles were predominant in all women in the study. None of the TNFA and IL18 alleles were associated with HPV infection. The results suggest that there is no relationship between TNF-308 G/A or IL18-607C/A polymorphisms and HPV infection among women in the study.

人类乳头瘤病毒(HPV)感染是全球最常见的性传播感染。持续感染可导致宫颈癌的发生,这可能是由于一些遗传因素造成的,如细胞因子基因调控区和编码区的多态性。本研究的目的是确定 TNF-308 G/A 或 IL18 多态性与布基纳法索性活跃妇女高危 HPV 感染之间是否存在关系。研究筛选了 91 名感染 HPV 的女性和 29 名 HPV 阴性的女性(后者作为健康对照)。采用 TaqMan 等位基因辨别法检测了 TNFA-308 G/A 和 IL18-607 C/A 多态性。最常见的 HPV 基因型为 HPV 52(21.19%)、HPV 39(11.86%)和 HPV 33(11.02%)。TNFA-308A和IL18-607 C等位基因在研究中的所有女性中都占主导地位。TNFA和IL18等位基因均与HPV感染无关。结果表明,TNF-308 G/A或IL18-607C/A多态性与研究中妇女的HPV感染没有关系。
{"title":"Association of TNF-α-308G/A and IL-18 Polymorphisms with risk of HPV infection among sexually active women in Burkina Faso.","authors":"Ina M A Traore, Théodora M Zohoncon, Florencia W Djigma, T Rebeca Compaore, Yves Traore, Jacques Simpore","doi":"10.1515/bmc-2020-0008","DOIUrl":"10.1515/bmc-2020-0008","url":null,"abstract":"<p><p>Human papillomavirus (HPV) infection is the most common sexually transmitted infection worldwide. Persistence infection can lead to the development of cervical cancer potentially due to some genetic factors such as polymorphisms in regulatory and coding regions of cytokine genes. The purpose of this study was to determine whether there is a relationship between TNF-308 G/A or IL18 polymorphisms and high-risk HPV infection among sexually active women from Burkina Faso. Ninety-one HPV infected and two hundred and nine HPV negative women (the latter used as healthy controls) were screened. TNFA-308 G/A and IL18-607 C/A polymorphisms were detected using the TaqMan allelic discrimination. HPV 52 (21.19%), HPV 39 (11.86%) and HPV 33 (11.02%) were the most common HPV genotypes. The TNFA-308A and IL18-607 C alleles were predominant in all women in the study. None of the TNFA and IL18 alleles were associated with HPV infection. The results suggest that there is no relationship between TNF-308 G/A or IL18-607C/A polymorphisms and HPV infection among women in the study.</p>","PeriodicalId":38392,"journal":{"name":"Biomolecular Concepts","volume":"11 1","pages":"97-101"},"PeriodicalIF":0.0,"publicationDate":"2020-04-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10012327","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
期刊
Biomolecular Concepts
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