CSHL Protein Homeostasis in Health and Disease Conference
CSHL 健康与疾病中的蛋白质稳态会议
基本信息
- 批准号:9470420
- 负责人:
- 金额:$ 3.07万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2017
- 资助国家:美国
- 起止时间:2017-09-15 至 2018-08-31
- 项目状态:已结题
- 来源:
- 关键词:AddressAffectAgingAging-Related ProcessAlpha CellAlzheimer&aposs DiseaseAmino AcidsAmyloidosisAnimal ModelAreaAttentionBasic ScienceBindingBiochemicalBiogenesisBiologyBiomedical ResearchBiophysicsBusinessesCell CompartmentationCell physiologyCellsCharacteristicsClientCommunicable DiseasesCommunitiesComplementComplexDataDevelopmentDiabetes MellitusDimensionsDisciplineDiseaseEnsureEnvironmentEquilibriumExplosionFacultyFailureFeedbackFinancial SupportFire - disastersFosteringFutureGeneral PopulationGoalsHealthHeartHeart DiseasesHeat shock proteinsHeat-Shock ResponseHomeostasisHormonesHuntington DiseaseIn VitroIndustryInternationalJournalsKnowledgeLaboratoriesMalignant NeoplasmsMeasuresMetabolic DiseasesMetabolismMethodsMolecularMolecular ChaperonesNerve DegenerationNeurodegenerative DisordersOralOrganismParkinson DiseaseParticipantPathogenicityPathway interactionsPeptide HydrolasesPhysiologyPlayPolymersPostdoctoral FellowPrion DiseasesProcessProtein ConformationProteinsPublishingQuality ControlQuestionnairesRecording of previous eventsResearch InstituteResearch PersonnelRibosomal ProteinsRibosomesRoleScheduleScienceScientistSignal TransductionSlideStressThinkingTimeToxic effectTranslatingWorkage effectage relatedcell typedisorder riskgraduate studenthealthy agingin vivoinsightinterestlecturesmeetingsnovelpolypeptidepostersprotein aggregationprotein degradationprotein foldingprotein functionprotein misfoldingproteostasisrepairedresponsesuccesssymposiumtumor metabolismvirtual
项目摘要
Cold Spring Harbor Laboratory Conference on
Protein Homeostasis in Health and Disease
April 17 – 21, 2018
ABSTRACT
This proposal is a request for financial support for a meeting on PROTEIN HOMEOSTASIS IN
HEALTH AND DISEASE to be held at Cold Spring Harbor Laboratory from April 17 – 21, 2018.
This meeting is the premier international forum for presentation of new results in this area, and
is attended by representatives from virtually every major laboratory in the field. The explosion of
new information on how the folded state of proteins is acquired and maintained in vivo and the
relevance of this process to healthy aging and diseases of neurodegeneration, cancer, and
metabolism guarantees an excitement and urgency of this meeting. Because of the recent
developments that have identified the ribosome at the origin of protein folding, we will have a
new session on this topic and another new session that emphasizes emerging quality control
mechanisms. The relationship between synthesis, folding, translocation and degradation will be
addressed through sessions on molecular mechanisms of chaperone function, degradative
mechanisms and on spatial quality control and organellar proteostasis. These fundamental
questions are at the heart of biology and will be complemented by sessions on aging and
proteostasis failure, and how this establishes the risk for diseases of protein misfolding including
Alzheimer's disease, ALS, Parkinson's disease and Huntington's disease. The themes of aging,
proteostasis failure, and diseases of protein misfolding will be integrated throughout the
meeting, and emerging principles on protein client interactions and alternate protein
conformations will be predominantly displayed. The diverse protein quality control strategies
used by compartments of the cell to ensure the integrity of the secretory and organellar
pathways during times of protein folding stress will be represented by emerging topics on spatial
quality control within a cell. The field of heat shock proteins and molecular chaperones has
grown exponentially and draws interest not only from traditional scientific disciplines in the basic
sciences but also from diverse areas of biomedical research including neurodegenerative
disease, infectious diseases, cancer, heart disease and aging. The meeting will have eight
lecture sessions, two poster sessions, a rapid-fire presentation session, and a panel discussion
on scientific publishing. The proposed sessions include: 1) Proteostasis at the ribosome and
protein folding, 2) Chaperone mechanisms I, 3) Novel mechanisms of quality control, 4)
Degradation mechanisms, 5) Chaperone mechanisms II, 6) Aging and pathogenic aggregation,
7) Organellar proteostasis and spatial quality control, and 8) Proteostasis failure and disease.
Each session will consist of eight to nine oral presentations and will be chaired by an invited
speaker. A maximum of two additional speakers will be pre-invited per session and the
remainder will be selected from submitted abstracts. This balance of talks allows the meeting to
feature presentations by leading scientists, to be responsive to exciting new developments, and
to encourage diverse participation that recognizes new investigators.
冷春港实验室会议
蛋白质稳态在健康和疾病中
2018年4月17日至21日
抽象的
该提案是为蛋白质稳态会议的会议的要求
健康和疾病将于2018年4月17日至21日在冷泉港实验室举行。
这次会议是在该领域介绍新结果的主要国际论坛,
通过代表该领域的每个主要实验室的代表来参加。爆炸
有关如何在体内获取和维持蛋白质折叠状态的新信息
该过程与神经变性,癌症和
代谢保证了这次会议的兴奋和紧迫性。因为最近
已经鉴定出蛋白质折叠起源的核糖体的发展,我们将有一个
有关此主题的新会议以及另一个强调新兴质量控制的新会议
机制。合成,折叠,易位和降解之间的关系将是
通过会议解决伴侣功能的分子机制,降解
机理和空间质量控制和有机蛋白质的机制。这些基本
问题是生物学的核心,将由有关衰老的会议完成
蛋白质抑制衰竭,以及如何确定蛋白质疾病错误折叠的风险
阿尔茨海默氏病,ALS,帕金森氏病和亨廷顿氏病。衰老的主题,
蛋白质衰竭和蛋白质错误折叠疾病将整合到整个过程中
蛋白质客户相互作用和替代蛋白质的会议和新兴原则
构象将主要显示。多样的蛋白质质量控制策略
由细胞隔室使用以确保秘密和细胞器的完整性
蛋白质折叠应力时期的途径将由空间上的新兴主题表示
单元内的质量控制。热激蛋白和分子伴侣的领域具有
成倍成长,不仅从基本的传统科学学科中吸引了兴趣
科学以及来自生物医学研究的潜水区域,包括神经退行性
疾病,传染病,癌症,心脏病和衰老。会议将有八个
演讲会议,两次海报会议,迅速演示会议和小组讨论
关于科学出版。拟议的会话包括:1)核糖体处的蛋白质静脉曲张和
蛋白质折叠,2)伴侣机制i,3)质量控制的新型机制,4)
降解机制,5)伴侣机制II,6)衰老和致病性聚集,
7)细胞器蛋白质和空间质量控制,以及8)蛋白质衰竭和疾病。
每个会议将由八到九个口头演讲组成,并由受邀的主持人主持
扬声器。每个会话最多将预先提前两个扬声器
其余部分将从提交的摘要中选择。这种谈判的平衡使会议得以
领先科学家的功能演讲,以应对令人兴奋的新发展,并
鼓励潜水员参与认可新研究人员。
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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DAVID J. STEWART其他文献
DAVID J. STEWART的其他文献
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