芝麻是八大类食物过敏原之一,快速准确识别芝麻过敏原对预防其过敏有重要意义。核酸适配体可以高效识别靶标过敏原,在过敏原检测中有良好的应用前景。为了获得芝麻主要过敏原Ses i 2的特异性核酸适体,本研究以Ses i 2为靶标,通过磁珠筛...芝麻是八大类食物过敏原之一,快速准确识别芝麻过敏原对预防其过敏有重要意义。核酸适配体可以高效识别靶标过敏原,在过敏原检测中有良好的应用前景。为了获得芝麻主要过敏原Ses i 2的特异性核酸适体,本研究以Ses i 2为靶标,通过磁珠筛选法(磁珠-SELEX)开展10轮筛选,经由高通量测序获得6条候补序列(S1~S6),并进行家族性、同源性分析及二级结构预测。结果表明,6条候选核酸适体的重复率可达46.38%,其自由能在-9.02到-2.47 kcal·moL^(-1)之间,根据自由能能量稳定原则,S1和S5吉布斯自由能最低最稳定,分别为-6.70和-9.02 kcal·moL^(-1)。利用ELISA试验进行亲和力测试,结果表明核酸适体S1和S2的亲和能力较强,S1:KD=67.02 nmol·L^(-1),R2=0.925 8,S2:KD=97.65 nmol·L^(-1),R2=0.795 1。核酸适体S1与过敏原Ses i 2的结合力和其他过敏原蛋白相比有显著差异,可视为具有特异性。本研究最终获得一条兼具良好亲和力和特异性的核酸适体S1,为芝麻过敏原快速检测提供了技术支撑。展开更多
Semen samples collected from 28 male partners of infertile couples were divided into three equal aliquots and prepared with three selected media,such as PureSperm (Nidacon,Gothenburg,Sweden),Sil-Select Plus^TM (Fer...Semen samples collected from 28 male partners of infertile couples were divided into three equal aliquots and prepared with three selected media,such as PureSperm (Nidacon,Gothenburg,Sweden),Sil-Select Plus^TM (Fertipro,Beemem,Belgium) and SpermGrad^TM(Vitrolife,Gothenburg,Sweden). The differences in mean percentages of semen parameters were assessed by repeated measures analysis. Correlations of sperm DNA damage,as measured by terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) assay,and of protamine deficiency,as measured by chromomycin A3 (CMA3) staining with sperm parameters,were determined by Pearson's correlation. After preparation with all three media,sperm concentrations decreased (P〈0.05) while percentages of sperm with normal morphology increased (P〈0.05). Percentages of sperm motility,rapid motility and progressive motile concentration (PMC) increased (P〈0.05) for each ofthese parameters,PureSperm preparation gave the best results (P〈0.05). The percentage of DNA damage decreased in the PureSperm and Sil-Select Plus preparations (17.9% and 31.3%,respectively,P〈0.05) and increased in the SpermGrad preparation (56.3%,P〈0.05). Protamine deficiency also decreased in all three kinds of media,59.3%,47.7% and 40.3% for PureSperm,Sil-Select Plus and SpermGrad preparations,respectively (P〈0.05). The percentage of DNA-damaged sperm was negatively correlated with the percentages of sperm motility,rapid motility and PMC,but was positively correlated with static motility (P〈0.05). This comparative study and correlation analysis revealed that PureSperm preparation yielded sperm with the best motility and the lowest percentage of protamine deficiency. The Sil-Select Plus preparation yielded sperm with the lowest amount of DNA damage. The SpermGrad preparation had a high percentage of sperm with normal morphology,but also had the highest percentage of sperm with DNA damage. Sperm DNA damage was correlated with percentages of sperm motility,rapid motility,static motility and PMC.展开更多
根据蓝印花布纹样的风格特征,文章提出一种端到端的蓝印花布纹样自动生成方法,实现简笔画图像向蓝印花布单纹样的自动迁移。针对蓝印花布的抽象风格和小数据集问题,重新构造CycleGAN生成网络中的编码器和解码器,使用SE(squeeze and exci...根据蓝印花布纹样的风格特征,文章提出一种端到端的蓝印花布纹样自动生成方法,实现简笔画图像向蓝印花布单纹样的自动迁移。针对蓝印花布的抽象风格和小数据集问题,重新构造CycleGAN生成网络中的编码器和解码器,使用SE(squeeze and excitation)注意力模块和残差模块与原始的卷积模块串联,提高特征提取能力和网络学习能力。同时减少生成网络中转换器的残差块层数,降低过拟合。实验结果表明,基于SE注意力CycleGAN网络方法自动生成的蓝印花布新纹样主观性上更贴合原始风格,与原图更加接近,有助于蓝印花布的数字化传承和创新。展开更多
Protamines are a group of highly basic proteins first discovered in spermatozoon that allow for denser packaging of DNA than histones and will result in down-regulation of gene transcription^l~. It is well recognized ...Protamines are a group of highly basic proteins first discovered in spermatozoon that allow for denser packaging of DNA than histones and will result in down-regulation of gene transcription^l~. It is well recognized that the Autographa californica multicapsid nucleopolyhedrovirus (AcMNPV) encodes P6.9, a protamine-like protein that forms the viral subnucleosome through binding to the viral genome[29]. Previous research demonstrates that P6.9 is essential for viral nucleocapsid assembly, while it has no influence on viral genome replication1311. In the present study, the role of P6.9 in viral gene transcription regulation is characterized. In contrast to protamines or other protamine-like proteins that usually down-regulate gene transcription, P6.9 appears to up-regulate viral gene transcription at 12-24 hours post infection (hpi), whereas it is non-essential for the basal level of viral gene transcription. Fluorescence microscopy reveals the P6.9's co-localization with DNA is temporally and spatially synchronized with P6.9's impact on viral gene transcription, indicating the P6.9-DNA association contributes to transcription regulation. Chromatin fractionation assay further reveals an unexpected co-existence of P6.9 and host RNA polymerase II in the same transcriptionally active chromatin fraction at 24 hpi, which may probably contribute to viral gene transcription up-regulation in the late infection phase.展开更多
Protamine is a kind small, basic protein rich in arginine residues and found to be complexed with DNA in spermatozoa. We have cloned a 150 bp cDNA encoding the rat protamine (rP) by RT PCR technique. Dig labelled...Protamine is a kind small, basic protein rich in arginine residues and found to be complexed with DNA in spermatozoa. We have cloned a 150 bp cDNA encoding the rat protamine (rP) by RT PCR technique. Dig labelled cDNA for rP was used for Northern blot analysis to study the expression of P1 protamine gene in rat and mouse. P1 protamine mRNA was detected only in rat testis, no hybridization signals were detected in rat brain and lever. In addition, the presence of P1 protamine mRNA was detected not only in rat testis, but also in mouse testis. Dig labelled cDNA for mouse protamine 1 (mP1) was used to study the expression of mP1 gene during the process of sexual maturation of mouse. 7~8 d after birth, no mP1 mRNA could be detected. At d 24~26, mP1 mRNA was detectable migrating as a homogeneous band at 580 nucleotides, whereas in sexually mature animals, a heterogeneous mixture of RNAs ranging from 450~580 bases in length was observed. Histological studies revealed that in the testis of 7~8 day old mouse, spermatogenesis has developed to the spermatocyte stage, whereas round spermatids (Rs) were present in the testis of the mice with 24~26 d age and elongating spermatids (Es) were present in the testis of sexually mature animals. Electrophoresis of total nuclear basic proteins (TNBP) revealed that the Rs could possess the somatic histones, while Es was found to have protamine and less histone. These results indicate that the P1 protamine gene is tissues specifically expressed and the P1 protamine is showing to be conservative in evolution. During the process of sexual maturation, along with morphological changes, mP1 gene was transcribed in Rs and translated in Es. The mechanism of protamine gene expression was discussed.展开更多
<abstract>During spermiogenesis, the protamine proteins play an integral role in spermatid chromatin compaction. Recent research has focused on many facets of protamine biology, including protamine gene and prot...<abstract>During spermiogenesis, the protamine proteins play an integral role in spermatid chromatin compaction. Recent research has focused on many facets of protamine biology, including protamine gene and protein structure/ function relationships, mechanisms of protamine expression regulation and involvement of the protamines in male fertility. In this paper, we review our current understanding of the structure and function of the protamine-1 (P1) and protamine-2 (P2) proteins and genes, the expression and regulation of these genes and the relationship between the protamines and male fertility. In addition, we offer a brief outlook on future investigation into protamine proteins.展开更多
近年来,中央银行数字货币(CBDC)受到全球多个国家和地区的高度关注.双离线交易作为CBDC的可选属性,在无网络连接的情况下进行支付,被认为具有较大的实用价值.面向CBDC的双离线匿名支付场景,基于可信执行环境(TEE)和安全单元(SE)技术,提...近年来,中央银行数字货币(CBDC)受到全球多个国家和地区的高度关注.双离线交易作为CBDC的可选属性,在无网络连接的情况下进行支付,被认为具有较大的实用价值.面向CBDC的双离线匿名支付场景,基于可信执行环境(TEE)和安全单元(SE)技术,提出了一种专为移动平台设计的高效双离线匿名支付方案(dual offline anonymous E-payment for mobile devices,OAPM).OAPM适用于资源受限的移动设备,允许移动付款者在不联网状态下安全地向收款者支付数字货币,且不向收款者及商业银行泄露个人隐私信息,付款者的支付行为也不会被链接,同时允许收款者设备处于离线状态,监管机构(如中央银行)在必要情况下能够识别匿名付款者的真实身份.该方案满足数字货币交易的多项重要属性,包括正确性、不可链接性、可追踪性、不可陷害性、机密性、真实性、防双花性以及可控匿名性等.实现了原型系统,并对可能的参数进行了评估.安全性分析和实验结果表明,该方案从安全性和效率两方面均能满足移动用户CBDC双离线交易的实际需求.展开更多
With the advantage of fast charge transfer,heterojunction engineering is identified as a viable method to reinforce the anodes'sodium storage performance.Also,vacancies can effectively strengthen the Na+adsorption...With the advantage of fast charge transfer,heterojunction engineering is identified as a viable method to reinforce the anodes'sodium storage performance.Also,vacancies can effectively strengthen the Na+adsorption ability and provide extra active sites for Na+adsorption.However,their synchronous engineering is rarely reported.Herein,a hybrid of Co_(0.85)Se/WSe_(2) heterostructure with Se vacancies and N-doped carbon polyhedron(CoWSe/NCP)has been fabricated for the first time via a hydrothermal and subsequent selenization strategy.Spherical aberration-corrected transmission electron microscopy confirms the phase interface of the Co_(0.85)Se/WSe_(2) heterostructure and the existence of Se vacancies.Density functional theory simulations reveal the accelerated charge transfer and enhanced Na+adsorption ability,which are contributed by the Co_(0.85)Se/WSe_(2) heterostructure and Se vacancies,respectively.As expected,the CoWSe/NCP anode in sodium-ion battery achieves outstanding rate capability(339.6 mAh g^(−1) at 20 A g^(−1)),outperforming almost all Co/W-based selenides.展开更多
文摘芝麻是八大类食物过敏原之一,快速准确识别芝麻过敏原对预防其过敏有重要意义。核酸适配体可以高效识别靶标过敏原,在过敏原检测中有良好的应用前景。为了获得芝麻主要过敏原Ses i 2的特异性核酸适体,本研究以Ses i 2为靶标,通过磁珠筛选法(磁珠-SELEX)开展10轮筛选,经由高通量测序获得6条候补序列(S1~S6),并进行家族性、同源性分析及二级结构预测。结果表明,6条候选核酸适体的重复率可达46.38%,其自由能在-9.02到-2.47 kcal·moL^(-1)之间,根据自由能能量稳定原则,S1和S5吉布斯自由能最低最稳定,分别为-6.70和-9.02 kcal·moL^(-1)。利用ELISA试验进行亲和力测试,结果表明核酸适体S1和S2的亲和能力较强,S1:KD=67.02 nmol·L^(-1),R2=0.925 8,S2:KD=97.65 nmol·L^(-1),R2=0.795 1。核酸适体S1与过敏原Ses i 2的结合力和其他过敏原蛋白相比有显著差异,可视为具有特异性。本研究最终获得一条兼具良好亲和力和特异性的核酸适体S1,为芝麻过敏原快速检测提供了技术支撑。
文摘Semen samples collected from 28 male partners of infertile couples were divided into three equal aliquots and prepared with three selected media,such as PureSperm (Nidacon,Gothenburg,Sweden),Sil-Select Plus^TM (Fertipro,Beemem,Belgium) and SpermGrad^TM(Vitrolife,Gothenburg,Sweden). The differences in mean percentages of semen parameters were assessed by repeated measures analysis. Correlations of sperm DNA damage,as measured by terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) assay,and of protamine deficiency,as measured by chromomycin A3 (CMA3) staining with sperm parameters,were determined by Pearson's correlation. After preparation with all three media,sperm concentrations decreased (P〈0.05) while percentages of sperm with normal morphology increased (P〈0.05). Percentages of sperm motility,rapid motility and progressive motile concentration (PMC) increased (P〈0.05) for each ofthese parameters,PureSperm preparation gave the best results (P〈0.05). The percentage of DNA damage decreased in the PureSperm and Sil-Select Plus preparations (17.9% and 31.3%,respectively,P〈0.05) and increased in the SpermGrad preparation (56.3%,P〈0.05). Protamine deficiency also decreased in all three kinds of media,59.3%,47.7% and 40.3% for PureSperm,Sil-Select Plus and SpermGrad preparations,respectively (P〈0.05). The percentage of DNA-damaged sperm was negatively correlated with the percentages of sperm motility,rapid motility and PMC,but was positively correlated with static motility (P〈0.05). This comparative study and correlation analysis revealed that PureSperm preparation yielded sperm with the best motility and the lowest percentage of protamine deficiency. The Sil-Select Plus preparation yielded sperm with the lowest amount of DNA damage. The SpermGrad preparation had a high percentage of sperm with normal morphology,but also had the highest percentage of sperm with DNA damage. Sperm DNA damage was correlated with percentages of sperm motility,rapid motility,static motility and PMC.
文摘根据蓝印花布纹样的风格特征,文章提出一种端到端的蓝印花布纹样自动生成方法,实现简笔画图像向蓝印花布单纹样的自动迁移。针对蓝印花布的抽象风格和小数据集问题,重新构造CycleGAN生成网络中的编码器和解码器,使用SE(squeeze and excitation)注意力模块和残差模块与原始的卷积模块串联,提高特征提取能力和网络学习能力。同时减少生成网络中转换器的残差块层数,降低过拟合。实验结果表明,基于SE注意力CycleGAN网络方法自动生成的蓝印花布新纹样主观性上更贴合原始风格,与原图更加接近,有助于蓝印花布的数字化传承和创新。
基金the National Nature Science Foundations of China(31030027,30400271),the National Natural Science Foundations of China for Young Scholars(31000081)
文摘Protamines are a group of highly basic proteins first discovered in spermatozoon that allow for denser packaging of DNA than histones and will result in down-regulation of gene transcription^l~. It is well recognized that the Autographa californica multicapsid nucleopolyhedrovirus (AcMNPV) encodes P6.9, a protamine-like protein that forms the viral subnucleosome through binding to the viral genome[29]. Previous research demonstrates that P6.9 is essential for viral nucleocapsid assembly, while it has no influence on viral genome replication1311. In the present study, the role of P6.9 in viral gene transcription regulation is characterized. In contrast to protamines or other protamine-like proteins that usually down-regulate gene transcription, P6.9 appears to up-regulate viral gene transcription at 12-24 hours post infection (hpi), whereas it is non-essential for the basal level of viral gene transcription. Fluorescence microscopy reveals the P6.9's co-localization with DNA is temporally and spatially synchronized with P6.9's impact on viral gene transcription, indicating the P6.9-DNA association contributes to transcription regulation. Chromatin fractionation assay further reveals an unexpected co-existence of P6.9 and host RNA polymerase II in the same transcriptionally active chromatin fraction at 24 hpi, which may probably contribute to viral gene transcription up-regulation in the late infection phase.
文摘Protamine is a kind small, basic protein rich in arginine residues and found to be complexed with DNA in spermatozoa. We have cloned a 150 bp cDNA encoding the rat protamine (rP) by RT PCR technique. Dig labelled cDNA for rP was used for Northern blot analysis to study the expression of P1 protamine gene in rat and mouse. P1 protamine mRNA was detected only in rat testis, no hybridization signals were detected in rat brain and lever. In addition, the presence of P1 protamine mRNA was detected not only in rat testis, but also in mouse testis. Dig labelled cDNA for mouse protamine 1 (mP1) was used to study the expression of mP1 gene during the process of sexual maturation of mouse. 7~8 d after birth, no mP1 mRNA could be detected. At d 24~26, mP1 mRNA was detectable migrating as a homogeneous band at 580 nucleotides, whereas in sexually mature animals, a heterogeneous mixture of RNAs ranging from 450~580 bases in length was observed. Histological studies revealed that in the testis of 7~8 day old mouse, spermatogenesis has developed to the spermatocyte stage, whereas round spermatids (Rs) were present in the testis of the mice with 24~26 d age and elongating spermatids (Es) were present in the testis of sexually mature animals. Electrophoresis of total nuclear basic proteins (TNBP) revealed that the Rs could possess the somatic histones, while Es was found to have protamine and less histone. These results indicate that the P1 protamine gene is tissues specifically expressed and the P1 protamine is showing to be conservative in evolution. During the process of sexual maturation, along with morphological changes, mP1 gene was transcribed in Rs and translated in Es. The mechanism of protamine gene expression was discussed.
文摘<abstract>During spermiogenesis, the protamine proteins play an integral role in spermatid chromatin compaction. Recent research has focused on many facets of protamine biology, including protamine gene and protein structure/ function relationships, mechanisms of protamine expression regulation and involvement of the protamines in male fertility. In this paper, we review our current understanding of the structure and function of the protamine-1 (P1) and protamine-2 (P2) proteins and genes, the expression and regulation of these genes and the relationship between the protamines and male fertility. In addition, we offer a brief outlook on future investigation into protamine proteins.
文摘近年来,中央银行数字货币(CBDC)受到全球多个国家和地区的高度关注.双离线交易作为CBDC的可选属性,在无网络连接的情况下进行支付,被认为具有较大的实用价值.面向CBDC的双离线匿名支付场景,基于可信执行环境(TEE)和安全单元(SE)技术,提出了一种专为移动平台设计的高效双离线匿名支付方案(dual offline anonymous E-payment for mobile devices,OAPM).OAPM适用于资源受限的移动设备,允许移动付款者在不联网状态下安全地向收款者支付数字货币,且不向收款者及商业银行泄露个人隐私信息,付款者的支付行为也不会被链接,同时允许收款者设备处于离线状态,监管机构(如中央银行)在必要情况下能够识别匿名付款者的真实身份.该方案满足数字货币交易的多项重要属性,包括正确性、不可链接性、可追踪性、不可陷害性、机密性、真实性、防双花性以及可控匿名性等.实现了原型系统,并对可能的参数进行了评估.安全性分析和实验结果表明,该方案从安全性和效率两方面均能满足移动用户CBDC双离线交易的实际需求.
基金support from the Natural Science Foundation of Jilin Province(Grant No.20200201073JC)the National Natural Science Foundation of China(Grant No.52130101)+1 种基金Interdisciplinary Integration and Innovation Project of JLU(Grant No.JLUXKJC2021ZY01)the Fundamental Research Funds for the Central Universities.
文摘With the advantage of fast charge transfer,heterojunction engineering is identified as a viable method to reinforce the anodes'sodium storage performance.Also,vacancies can effectively strengthen the Na+adsorption ability and provide extra active sites for Na+adsorption.However,their synchronous engineering is rarely reported.Herein,a hybrid of Co_(0.85)Se/WSe_(2) heterostructure with Se vacancies and N-doped carbon polyhedron(CoWSe/NCP)has been fabricated for the first time via a hydrothermal and subsequent selenization strategy.Spherical aberration-corrected transmission electron microscopy confirms the phase interface of the Co_(0.85)Se/WSe_(2) heterostructure and the existence of Se vacancies.Density functional theory simulations reveal the accelerated charge transfer and enhanced Na+adsorption ability,which are contributed by the Co_(0.85)Se/WSe_(2) heterostructure and Se vacancies,respectively.As expected,the CoWSe/NCP anode in sodium-ion battery achieves outstanding rate capability(339.6 mAh g^(−1) at 20 A g^(−1)),outperforming almost all Co/W-based selenides.