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药物开发过程面临多重挑战,而靶标确证是其中的重要一环。如何运用多种研究方法发现和确认小分子药物的靶标是目前研究人员的主要工作内容之一。化学蛋白质组学整合了细胞生物学、合成化学和生物质谱等多门学科,为药物的靶标筛选提供了新平台。本文对近年来发展的基于生物质谱的化学蛋白质组学药物靶标鉴定技术进行了总结,结合具体应用分析其优缺点,并对该类技术的发展和应用进行总结和展望。 相似文献
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药物或生物活性物质通过与靶蛋白结合而发挥功能,研究表明,大多数药物具有多个作用靶点,药物靶标的发现有助于药物前体的筛选和作用机制的研究,同时对其耐药性等副作用的解决方案提供理论指导.基于生物质谱技术的蛋白质组学可对蛋白质进行高通量的定性定量分析,为药物靶标的筛选提供了全新的平台.本文综述了基于固载药物和游离药物模式的药物靶标蛋白筛选相关方法和应用研究的最新进展,为基于生物质谱技术的化学蛋白质组学研究提供参考. 相似文献
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化学基因组技术是药物作用靶标确认、药物分子在通路中的作用的确证等方面有重要应用,可为新药研发和老药新用提供理论依据,并可降低药物发现中的高额成本.精氨酸-甘氨酸-天冬氨酸(RGD)三肽被证明是与细胞粘附受体特异性结合的特征序列,在生理学上扮演者重要角色.本研究利用化学基因组学中的其中一种方法即基于反向对接和药效团反向匹配搜索技术来研究RGD三肽的潜在作用靶标,并进行计算机模拟分析.反向匹配搜索结果发现计算得到的关键性靶标及其涉及的相关疾病与实验报道的RGD的药理活性相吻合,包括具有抗凝血、抗肿瘤作用,与肾及心血管作用有关等,而且还发现RGD可能是一个潜在的神经氨酸酶的抑制剂. 相似文献
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《生物产业技术》编辑部 《生物产业技术》2008,(3):7-7
国家“863”计划现代农业技术领域通过攻关发现并鉴定了一系列基因和蛋白质新靶标,在农业生物药物分子设计平台建设方面取得可喜进展。 相似文献
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药物靶标的发现和验证是新药研发的关键环节,对新药创制具有源头创新意义。天然产物是新药创制的重要来源,识别其作用靶点不仅为临床预防治疗提供可能新策略,也为进一步阐释中草药及其复方的作用特点及分子机制提供参考依据。随着生命科学和信息学的发展,药物靶点的识别及确证方法不断涌现,生物信息学、网络药理学、蛋白质组学、亲和色谱、药物亲和稳定性、芯片技术、基因敲除技术、RNA干扰等技术的广泛应用,越来越多的天然活性成分的靶点得以识别和验证。因此,本文对近五年来天然活性成分作用靶点识别及确证方法做一简要综述,以供参考。 相似文献
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哺乳动物雷帕霉素靶蛋白(mTOR)是一种丝氨酸/苏氨酸激酶,可集合胞内和胞外信号调节细胞生长、增殖、代谢和存活。在肿瘤的发生发展过程中,mTOR信号多处于异常激活状态,已被确证为肿瘤药物治疗的重要靶标。因雷帕霉素临床应用存在局限性,近期ATP竞争性mTOR抑制剂的研发十分活跃。本文综述了ATP竞争性mTOR抑制剂的研究进展,重点讨论药物的作用特点。 相似文献
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药物与靶标的结合是启动药理作用的本源,共价键药物是以共享电子的方式来实现与靶标的结合,其中大多为抗感染、抗肿瘤以及心脑血管、神经系统和代谢类药物。简介共价键药物与非共价键药物的区别以及既往的重磅级共价键药物与靶标的结合特点,分类综述靶向共价键药物的理性设计及与靶标的结合反应。 相似文献
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药物的使用极大地提高了人类的生存质量。药物的有效性是药物发现研究中的关键环节。药物的有效性通过识别药物与其作用的靶标蛋白来判断。然而,通过高通量筛选的实验方法分析确定化合物药物-靶标蛋白互作关联是一个十分昂贵、耗时且富有挑战性的任务。基于计算方法的化合物药物-靶标蛋白互作关联预测研究具有效率高、成本低的特点,越来越受到人们的重视。相比实验验证方法,化合物药物-靶标蛋白互作关联的计算方法可为药物发现研究后续的生物药学实验提供更为准确的潜在化合物药物-靶标蛋白候选对,达到减少生物实验的时间和成本的目的。本文回顾了近20年来基于计算方法的化合物药物-靶标蛋白互作关联预测算法所涉及的生物医学特征数据、预测方法和技术,并分析研究过程中所面临的生物医学特征数据高维稀疏,以及多源生物医学数据融合程度不高等问题,为进一步研究提供有价值的参考。 相似文献
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Recent advances in the study of Kaposi's sarcoma-associated herpesvirus replication and pathogenesis
It has now been over twenty years since a novel herpesviral genome was identified in Kaposi's sarcoma biopsies. Since then, the cumulative research effort by molecular biologists, virologists, clinicians, and epidemiologists alike has led to the extensive characterization of this tumor virus, Kaposi's sarcoma-associated herpesvirus(KSHV; also known as human herpesvirus 8(HHV-8)), and its associated diseases. Here we review the current knowledge of KSHV biology and pathogenesis, with a particular emphasis on new and exciting advances in the field of epigenetics. We also discuss the development and practicality of various cell culture and animal model systems to study KSHV replication and pathogenesis. 相似文献
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正Dear Editor,In December 2019, a novel human coronavirus caused an epidemic of severe pneumonia(Coronavirus Disease 2019,COVID-19) in Wuhan, Hubei, China(Wu et al. 2020; Zhu et al. 2020). So far, this virus has spread to all areas of China and even to other countries. The epidemic has caused 67,102 confirmed infections with 1526 fatal cases 相似文献
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Curcumin is the yellow pigment of turmeric that interacts irreversibly forming an adduct with thioredoxin reductase (TrxR), an enzyme
responsible for redox control of cell and defence against oxidative stress. Docking at both the active sites of TrxR was performed to compare
the potency of three naturally occurring curcuminoids, namely curcumin, demethoxy curcumin and bis-demethoxy curcumin. Results show
that active sites of TrxR occur at the junction of E and F chains. Volume and area of both cavities is predicted. It has been concluded by
distance mapping of the most active conformations that Se atom of catalytic residue SeCYS498, is at a distance of 3.56 from C13 of
demethoxy curcumin at the E chain active site, whereas C13 carbon atom forms adduct with Se atom of SeCys 498. We report that at least
one methoxy group in curcuminoids is necessary for interation with catalytic residues of thioredoxin. Pharmacophore of both active sites of
the TrxR receptor for curcumin and demethoxy curcumin molecules has been drawn and proposed for design and synthesis of most probable
potent antiproliferative synthetic drugs. 相似文献
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RICHARD E. NORRIS 《Botanical journal of the Linnean Society. Linnean Society of London》1991,106(1):1-40
Comprises species occurring mostly in subtidal habitats in tropical, subtropical and warm-temperate areas of the world. An analysis of the type species, V. spiralis (Sonder) Lamouroux ex J. Agardh, a species from Australia, establishes basic characters for distinguishing species in the genus. These characters are (1) branching patterns of thalli, (2) flat blades that may be spiralled on their axis, (3) width of the blade, (4) primary or secondary derivation of sterile and fertile branchlets and (5) position of sterile and fertile branchlets on the thalli. Application of the latter two characters provides an important basic method for separation of species into three major groups. Osmundaria , a genus known only in southern Australia, was studied in relation to Vidalia , and its separation from the Vidalia assemblage is not accepted. Species of Vidalia therefore are transferred to the older genus name, Osmundaria. Two new species, Osmundaria papenfussii and Osmundaria oliveae are described from Natal. Confusion in the usage of the epithet, Vidalia fimbriala Brown ex Turner has been clarified, and Vidalia gregaria Falkenberg, described as an epiphyte on Osmundaria pro/ifera Lamouroux, is revealed to be young branches of the host, Osmundaria prolifera. 相似文献
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JOAN VALUÈS MONTSERRAT TORRELL NÚRIA GARCIA JACAS 《Botanical journal of the Linnean Society. Linnean Society of London》2001,137(4):399-407
Fifteen chromosome counts of six Artemisia taxa and one species of each of the genera Brachanthemum, Hippolytia, Kaschgaria, Lepidolopsis and Turaniphytum are reported from Kazakhstan. Three of them are new reports, two are not consistent with previous counts and the remainder are confirmations of very scarce (one to four) earlier records. All the populations studied have the same basic chromosome number, x = 9, with ploidy levels ranging from 2x to 6x. Some correlations between ploidy level, morphological characters and distribution are noted. 相似文献