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标题: Assembly's Zlotnick讨论公司的核心蛋白变构调节剂(CpAMs [打印本页]

作者: StephenW    时间: 2015-5-19 22:54     标题: Assembly's Zlotnick讨论公司的核心蛋白变构调节剂(CpAMs

Assembly Biosciences Discusses Mechanism of Action of Its HBV Antiviral Program at 2nd ANRS HBV Cure Workshop
By GlobeNewswire,  May 19, 2015, 07:30:00 AM EDT


Workshop Sponsored by French National Agency for Research on AIDS and Viral Hepatitis

NEW YORK and PARIS, May 19, 2015 (GLOBE NEWSWIRE) -- Assembly Biosciences, Inc. (Nasdaq:ASMB) today announced that Adam Zlotnick, PhD, Assembly's Chief Scientific Advisor and Chair of its HBV & Virology Science Advisory Board, discussed the science underlying the company's Core Protein Allosteric Modifiers (CpAMs) at the Second ANRS HBV Cure Workshop sponsored by the French National Agency for Research on AIDS and Viral Hepatitis (ANRS). Assembly's CpAMs are in development for the curative treatment of hepatitis B viral infection (HBV).

For more than 25 years, ANRS has played an important role in the global fight against HIV/AIDs. Recently ANRS added viral hepatitis to its mandate. The invitation-only HBV Cure Workshop brings together leading scientists whose work could advance the development of curative therapies for HBV.

Dr. Zlotnick, who conducted the seminal work on CpAMs in his laboratory at Indiana University, commented, "We wanted to share with our fellow scientists how Assembly's insights into the complexities of the HBV core protein and its lifecycle are informing our CpAM antiviral program. Our ability to leverage different classes of CpAMs to target allosteric properties of core protein allows us to engineer and select molecules that interfere with multiple locations in the viral lifecycle, both 'upstream' and 'downstream' of formation of the viral capsid."

In his presentation, Dr. Zlotnick described how the HBV core protein is not a single rigid defined structure, nor does it serve solely to assemble the capsid. Rather the core protein assumes multiple structures to accomplish a wide variety of different activities. The importance of its many functions makes core protein an excellent target for antiviral therapies. Additionally, the dynamic nature of the protein makes it susceptible to control by allosteric modifiers. While some researchers are focusing on self-assembly as the most accessible core protein activity for antiviral intervention, Assembly's antiviral program leverages the allosteric nature of the core protein's interactions to design modulators that engage the broader spectrum of core protein functions across the viral lifecycle. This broader approach is central to Assembly's program to develop clinically curative therapies for HBV.

Uri Lopatin, MD, Chief Medical Officer and Vice President of R&D at Assembly, also attended the Workshop. He noted, "We are delighted that Adam's thought leadership on core protein and its multiple functions is being recognized by the ANRS. Adam's presentation highlighted the protean nature of core protein along with preliminary data showing how our approach targets core protein both upstream and downstream in the lifecycle. This provides us a unique ability to generate distinctive allosteric molecules that can reduce viral replication, as well as the production of viral antigens such as HBsAg. Our growing understanding of the viral core protein is enabling us to make good progress in advancing the CpAM program, and the feedback and dialogue from today's workshop provided additional confidence that we are on the right track."

About Assembly Biosciences

Assembly Biosciences, Inc. is a public biopharmaceutical company developing novel oral therapies for the cure of intractable infectious diseases, focusing on hepatitis B virus (HBV) and C. difficile-associated (CDAD) infections. Its HBV-Cure research team is discovering and developing multiple Core protein Allosteric Modifiers (CpAMs) to modulate the HBV core protein—a polyfunctional essential viral protein-—at multiple complementary points in the viral lifecycle. The goal is to eradicate HBV infection with an orally-administered regimen. Assembly is uniquely positioned to execute on this strategy, with a senior scientific team that has over 30 years of combined experience working on HBV. The company's CDAD program is based on the targeted delivery of novel microbiome-based therapies in a proprietary oral formulation. Assembly has created a network of world-class microbiome scientists from academia and industry to help advance this innovative program. For more information visit assemblybio.com.   

Read more: http://www.nasdaq.com/press-rele ... 00284#ixzz3ab1grgn5


作者: StephenW    时间: 2015-5-19 22:54

它的抗病毒乙肝项目的行动在第2 ANRS乙肝防治研讨会大会讨论生物科学机制
通过GlobeNewswire,2015年5月19日,上午7点30分零零秒EDT


研讨会研究艾滋病和病毒性肝炎赞助法国国家机构

纽约和巴黎,2015年5月19日(GLOBE NEWSWIRE) - 生物科学大会,公司(纳斯达克股票代码:ASMB)今天宣布,亚当Zlotnick,博士,大会的首席科学顾问和乙肝病毒和科学顾问委员会主席,讨论的科学在第二ANRS乙肝治疗研讨会上研究艾滋病和病毒性肝炎(ANRS)主办的法国国家机构是公司的核心蛋白变构调节剂(CpAMs)底层。大会CpAMs正在开发用于治疗治疗乙肝病毒感染(HBV)。

对于超过25年,ANRS已在防治艾滋病毒/艾滋病的全球斗争中发挥了重要作用。最近ANRS增加病毒性肝炎其授权。邀请只HBV治疗研讨会汇集了著名科学家的工作可以促进治疗治疗的发展乙肝。

Zlotnick博士,谁在他的实验室在美国印第安纳大学进行了CpAMs的开创性工作,说:“我们希望与我们的同胞科学家们分享如何大会分析上市公司的乙肝病毒核心蛋白和其生命周期的复杂性是我们的通知CPAM抗病毒程序。我们能够利用不同类别CpAMs到目标核心蛋白的变构性的能力使我们可以设计并选择与在病毒生命周期中的多个位置干扰的分子,这两个“上游”和形成病毒衣壳的“下游”。“

在他的演讲,Zlotnick博士所描述的乙肝病毒核心蛋白怎么不是单一死板定义的结构,也不会都只是组装衣壳。而核心蛋白假定多个结构以完成各种不同的活动。它的许多功能的重要性,使核心蛋白一个很好的目标,抗病毒治疗。此外,蛋白质的动态性质使得它容易通过变构调节剂来控制。虽然一些研究人员的重点是自组装为抗病毒干预的最方便的核心蛋白的活动,大会的抗病毒程序利用了核心蛋白的相互作用的变构性设计从事的核心蛋白功能整个病毒生命周期的范围更广调制器。这种更广泛的方法是至关重要的大会的程序开发临床疗效的治疗乙肝。

乌里洛帕廷,医学博士,首席医疗官和R&D的大会副总裁也出席了研讨会。他指出,“我们很高兴看到在核心蛋白和多种功能亚当的思想领导是被公认的ANRS。亚当的发言强调核心蛋白的千变万化的性质与初步数据显示如何我们的方法针对核心蛋白的上游和下游的生命周期。这为我们提供了一个独特的能力,以产生独特的变构分子,可以减少病毒复制,以及生产病毒抗原如乙肝表面抗原,我们生长的病毒核心蛋白的理解是使我们能够使良好的进展在推进CPAM程序,从今天的研讨会的反馈和对话提供了更多的信心,我们是在正确的轨道。“

关于生物科学大会

大会Biosciences公司,公司是一家生物制药公众公司开发新型口服疗法对顽固性感染性疾病的治疗,重点对乙型肝炎病毒(HBV)和艰难梭菌相关(CDAD)感染。其HBV-CURE研究小组发现和开发多核心蛋白变构调节剂(CpAMs)调控HBV核心蛋白多官能必不可少的病毒蛋白 - 在多个互补点在病毒的生命周期。我们的目标是消除HBV感染用的口服疗法。大会专门定位于这一战略执行,拥有一支资深的科研团队,拥有超过30年的经验相结合,致力于乙肝病毒。该公司的CDAD方案是基于专有的口服制剂中的靶向递送的新型微生物为基础的治疗。大会创造了学术界和产业界的世界级科学家微生物组成的网络,以帮助推进这一创新方案。欲了解更多信息,请访问assemblybio.com。

阅读更多: http://www.nasdaq.com/press-rele ... 00284#ixzz3ab1grgn5
作者: tonychant    时间: 2015-5-20 19:28

何时进入临床?不看广告,看疗效。这一类软广告看的太多了,麻木了,不解决问题
作者: newchinabok    时间: 2015-5-20 19:35

2016年进1期,太慢了,就是碰碰运气吧

作者: 遥望曙光    时间: 2015-5-20 20:39

有的期待总比没有希望好。




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