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细粒棘球绦虫AgB1抗原表位的生物信息学预测 被引量:4
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作者 马秀敏 胡晓安 +4 位作者 阿尔孜古丽·吐尔逊 李艳华 刘学磊 朱明 丁剑冰 《科技导报》 CAS CSCD 北大核心 2013年第27期27-30,共4页
以细粒棘球绦虫AgB1基因序列为基础,采用Predict Protein软件预测其编码蛋白的二级结构;应用在线预测软件Bcepred、Abcpred、IEDB及SYFPEITHI等对细粒棘球绦虫AgB1的B细胞表位和T细胞表位进行预测。结果提示,AgB1抗原蛋白存在可以构... 以细粒棘球绦虫AgB1基因序列为基础,采用Predict Protein软件预测其编码蛋白的二级结构;应用在线预测软件Bcepred、Abcpred、IEDB及SYFPEITHI等对细粒棘球绦虫AgB1的B细胞表位和T细胞表位进行预测。结果提示,AgB1抗原蛋白存在可以构成抗原表位的区域。经软件分析,分值高的B细胞表位区域:2~9、15~20、22~35和41~52氨基酸序列;T细胞表位区域:3-12、26~33、34~44和52-61氨基酸序列。研究运用生物信息学确定AgB1抗原的4个B细胞优势表位和4个T细胞优势表位。对进一步研究AqB1的抗原性和研发更有价值的免疫诊断方法具有重要意义。 展开更多
关键词 agb1 B细胞表位 T细胞表位 生物信息学
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Photoexcited CRYPTOCHROME 1 Interacts Directly with G-Protein 13 Subunit AGB1 to Regulate the DNA-Binding Activity of HY5 and Photomorphogenesis in Arabidopsis 被引量:11
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作者 Hongli Lian Pengbo Xu +8 位作者 Shengbo He Jun Wu Jian Pan Wenxiu Wang Feng Xu Sheng Wang Junsong Pan Jirong Huang Hong-Quan Yang 《Molecular Plant》 SCIE CAS CSCD 2018年第10期1248-1263,共16页
Light and the heterotrimeric G-protein are known to antagonistically regulate photomorphogenesis in Arabidopsis. However, whether light and G-protein coordinate the regulation of photomorphogenesis is largely unknown.... Light and the heterotrimeric G-protein are known to antagonistically regulate photomorphogenesis in Arabidopsis. However, whether light and G-protein coordinate the regulation of photomorphogenesis is largely unknown. Here we show that the blue light photoreceptor cryptochrome 1 (CRY1) physically inter-acts with the G-protein β subunit, AGB1, in a blue light-dependent manner. We also show that AGB1 directly interacts with HY5, a basic leucine zipper transcriptional factor that acts as a critical positive regulator of photomorphogenesis, to inhibit its DNA-binding activity. Genetic studies suggest that CRY1 acts partially through AGB1, and AGB1 acts partially through HY5 to regulate photomorphogenesis. Moreover, we demonstrate that blue light-triggered interaction of CRY1 with AGB1 promotes the dissociation of HY5 from AGB1. Our results suggest that the CRY1 signaling mechanism involves positive regulation of the DNA-binding activity of HY5 mediated by the CRY1-AGB1 interaction, which inhibits the association of AGB1 with HY5. We propose that the antagonistic regulation of HY5 DNA-binding activity by CRY1 and AGB1 may allow plants to balance light and G-protein signaling and optimize photomorphogenesis. 展开更多
关键词 ARABIDOPSIS CRYPTOCHROME heterotrimeric G-protein β subunit agb1 HY5 PHOTOMORPHOGENESIS
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Phytochrome B and AGB1 Coordinately Regulate Photomorphogenesis by Antagonistically Modulating PIF3 Stability in Arabidopsis 被引量:5
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作者 Pengbo Xu Hongli Lian +6 位作者 Feng Xu Ting Zhang Sheng Wang Wenxiu Wang Shasha Du Jirong Huang Hong-Quan Yang 《Molecular Plant》 SCIE CAS CSCD 2019年第2期229-247,共19页
Phytochrome B (phyB), the primary red light photoreceptor, promotes photomorphogenesis in Arabidopsis by interacting with the basic helix-loop-helix transcriptional factor PIF3 and inducing its phosphorylation and deg... Phytochrome B (phyB), the primary red light photoreceptor, promotes photomorphogenesis in Arabidopsis by interacting with the basic helix-loop-helix transcriptional factor PIF3 and inducing its phosphorylation and degradation. Heterotrimeric G proteins are known to regulate various developmental processes in plants and animals. In Arabidopsis, the G-protein β subunit AGB1 is known to repress photomorphogenesis. However, whether and how phyB and AGB1 coordinately regulate photomorphogenesis are largely unknown. Here we show that phyB physically interacts with AGB1 in a red light-dependent manner and that AGB1 interacts directly with PIF3. Moreover, we demonstrate that the AGB1-PIF3 interaction inhibits the association of PIF3 with phyB, leading to reduced phosphorylation and degradation of PIF3, whereas the phyB-AGB1 interaction represses the association of PIF3 with AGB1, resulting in enhaneed phosphorylation and degradation of PIF3. Our results suggest that phyB and AGB1 antagonistically regulate PIF3 stability by dynamically interacting with each other and PIF3. This dynamic mechanism may allow plants to balanee phyB and G-protein signaling to optimize photomorphogenesis. 展开更多
关键词 ARABIDOPSIS PHYTOCHROME B heterotrimeric G-PROTEIN β sub unit agb1 PIF3 PHOTOMORPHOGENESIS protein STABILITY
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Arabidopsis cryptochrome 1 promotes stomatal development through repression of AGB1 inhibition of SPEECHLESS DNA-binding activity 被引量:1
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作者 Xiaoli Cao Pengbo Xu +11 位作者 Yao Liu Guangqiong Yang Minqing Liu Li Chen Yingyu Cheng Peng Xu Langxi Miao Zhilei Mao Wenxiu Wang Shuang Kou Tongtong Guo Hong‐Quan Yang 《Journal of Integrative Plant Biology》 SCIE CAS CSCD 2021年第11期1967-1981,共15页
Cryptochromes are blue light photoreceptors that mediate various light responses in plants and mammals. The heterotrimeric G-protein is known to regulate various physiological processes in plants and mammals. In Arabi... Cryptochromes are blue light photoreceptors that mediate various light responses in plants and mammals. The heterotrimeric G-protein is known to regulate various physiological processes in plants and mammals. In Arabidopsis, cryptochrome 1(CRY1) and the G-protein β subunit AGB1 act antagonistically to regulate stomatal development.The molecular mechanism by which CRY1 and AGB1 regulate this process remains unknown.Here, we show that Arabidopsis CRY1 acts partially through AGB1, and AGB1 acts through SPEECHLESS(SPCH), a master transcription factor that drives stomatal initiation and proliferation, to regulate stomatal development. We demonstrate that AGB1 physically interacts with SPCH to block the b HLH DNA-binding domain of SPCH and inhibit its DNA-binding activity. Moreover, we demonstrate that photoexcited CRY1 represses the interaction of AGB1 with SPCH to release AGB1 inhibition of SPCH DNA-binding activity, leading to the expression of SPCH-target genes promoting stomatal development. Taken together, our results suggest that the mechanism by which CRY1 promotes stomatal development involves positive regulation of the DNA-binding activity of SPCH mediated by CRY1 inhibition of the AGB1-SPCH interaction. We propose that the antagonistic regulation of SPCH DNA-binding activity by CRY1 and AGB1 may allow plants to balance light and G-protein signaling and optimize stomatal density and pattern. 展开更多
关键词 cryptochrome 1(CRY1) heterotrimeric G-proteinβ-subunit agb1 SPEECHLESS DNA-binding activity stomatal development
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细粒棘球绦虫AgB8/1-AgB8/2重组嵌合抗原表达系统的构建 被引量:1
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作者 古力帕丽.麦曼提依明 马海梅 +5 位作者 吾拉木.马木提 陈洁 陈璐 丁剑冰 马秀敏 温浩 《中国人兽共患病学报》 CAS CSCD 北大核心 2011年第6期502-505,510,共5页
目的构建pET32a-AgB8/1-AgB8/2原核表达载体,并对其重组蛋白进行原核细胞表达。方法从细粒棘球绦虫原头蚴中提取总RNA,反转录生成cDNA,以此cDNA为模板,用基因特异性引物分别扩增EgAgB8/1和EgAgB8/2基因编码其分泌型多肽的片段,经测序后... 目的构建pET32a-AgB8/1-AgB8/2原核表达载体,并对其重组蛋白进行原核细胞表达。方法从细粒棘球绦虫原头蚴中提取总RNA,反转录生成cDNA,以此cDNA为模板,用基因特异性引物分别扩增EgAgB8/1和EgAgB8/2基因编码其分泌型多肽的片段,经测序后,以此两条基因片段为依据,人工合成EgAgB8/1-EgAgB8/2嵌合抗原编码核酸序列,将其克隆至pUCm-T载体,测序鉴定其正确性。通过对pUCm-T/AgB8/1-AgB8/2重组质粒进行双酶切,将获得的AgB8/1-AgB8/2嵌合抗原编码核酸序列用定向克隆技术克隆至原核表达质粒pET32a上,测序鉴定插入片段正确后,转化至E.coliBL21(DE3)Lys S,IPTG初步诱导表达pET32a-AgB8/1-AgB8/2重组嵌合蛋白。用SDS-PAGE电泳分析鉴定重组蛋白的表达水平。结果测序表明,AgB8/1-AgB8/2嵌合抗原编码核酸序列正方向插入至pET32a质粒。SDS-PAGE电泳分析显示,IPTG诱导后重组嵌合蛋白得到成功表达,在相对分子量约38 kD处有表达条带。结论成功构建了pET32a-AgB8/1-AgB8/2原核表达质粒,并初步诱导表达出AgB8/1-AgB8/2嵌合重组蛋白,为进一步研究其免疫学特性奠定了基础。 展开更多
关键词 细粒棘球绦虫 AgB8/1-AgB8/2重组嵌合抗原 原核表达质粒
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细粒棘球绦虫AgB8/1重组抗原表达系统的构建 被引量:1
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作者 古力帕丽.麦曼提依明 马海梅 +2 位作者 陈洁 陈璐 吾拉木.马木提 《新疆医科大学学报》 CAS 2011年第3期246-250,共5页
目的构建pET32a-AgB8/1原核表达载体,并对其重组蛋白进行原核细胞表达。方法从细粒棘球绦虫原头蚴中提取总RNA,反转录生成cDNA,以此cDNA为模板用基因特异性引物扩增EgAgB8/1基因编码其分泌型多肽的片段,经测序后,以此基因片段为依据,人... 目的构建pET32a-AgB8/1原核表达载体,并对其重组蛋白进行原核细胞表达。方法从细粒棘球绦虫原头蚴中提取总RNA,反转录生成cDNA,以此cDNA为模板用基因特异性引物扩增EgAgB8/1基因编码其分泌型多肽的片段,经测序后,以此基因片段为依据,人工合成合成EgAgB8/1抗原编码核酸序列,将其克隆至pUCm-T载体,测序鉴定其正确性。通过对pUCm-T/AgB8/1重组质粒进行双酶切,将获得的AgB8/1抗原编码核酸序列用定向克隆技术克隆至原核表达质粒pET32a上,测序鉴定插入片段正确性后,转化至E.coli BL21(DE3)Lys S,IPTG初步诱导表达pET32a-AgB8/1重组蛋白。用SDS-PAGE电泳分析鉴定重组蛋白的表达水平。结果测序表明,AgB8/1抗原编码核酸序列正方向插入至pET32a质粒。SDS-PAGE电泳分析显示,IPTG诱导后重组蛋白得到成功表达,在相对分子量约28 kDa处有表达条带。结论本研究成功构建了pET32a-AgB8/1原核表达质粒,并初步诱导表达出AgB8/1重组蛋白,为进一步研究其免疫学特性奠定了基础。 展开更多
关键词 细粒棘球绦虫 AgB8/1重组抗原 原核表达质粒
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