STRUCTURE/FUNCTIONAL ANALYSIS OF INHIBIN
STRUCTURE/FUNCTIONAL ANALYSIS OF INHIBIN
批准号:
2026393
负责人:
AARON JW HSUEH
金额:
$8.05万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
1997
资助国家:
美国
项目状态:
已结题
起止时间:
1997-04-01 至 1999-03-31
中文摘要
描述(改编自申请人描述):抑制素和激活素
是相关的性腺蛋白激素,分别抑制或
通过垂体促性腺作用刺激FSH释放。 最近的研究表明
促性腺激素α和β亚基cDNA的串联融合赋予了
二聚体蛋白的有效分泌,而不影响它们的
生物活性 基于两种蛋白质之间的结构相似性,
促性腺激素,它是假设,融合的α和β的促性腺激素,
亚单位cDNA可能允许有效表达和分泌的
异二聚体。 初步数据表明,
通过合成白藜芦醇,
在β和α亚基cDNA融合后的二聚体。 拟
为了进一步表征通过该方法产生的Escherichia bin同种型,
通过分离已知的细胞系,
含有对前蛋白加工重要的蛋白水解酶。 的
突变体类胡萝卜素同工型生物活性和结构-功能
分析以阐明N-连接的碳水化合物侧链的重要性。
预计这些研究将导致更好的设计,
本发明提供了一种新的腺苷酸激动剂和拮抗剂,
临床应用的重组人胰蛋白酶。
英文摘要
DESCRIPTION (Adapted from applicants description): Inhibins and activins
are related gonadal protein hormones that, respectively, inhibit or
stimulate FSH release by pituitary gonadotrophy. Recent studies suggest
that tandem fusion of gonadotropin alpha and beta subunit cDNAs confers
efficient secretion of the dimer proteins without affecting their
bioactivities. Based on the structural similarity between inhibins and
gonadotropins, it is hypothesized that fusion of the inhibin alpha and beta
subunit cDNAs might allow efficient expression and secretion of the
heterodimer. The preliminary data indicated that earlier difficulties in
producing inhibin over activin can be overcome by synthesizing inhibin
dimers following fusion of the beta and alpha subunit cDNAs. It is proposed
to further characterize the inhibin isoforms produced by this method and to
increase the processing of mature inhibins by transfecting cell lines known
to contain proteolytic enzymes important for pro-protein processing. The
bioactivity of mutant inhibin isoforms and perform structure-functional
analysis to elucidate the importance of N-linked carbohydrate side chains.
It is anticipated that these studies would lead to a better design of
inhibin agonists and antagonists as well as efficient production of
recombinant inhibins of clinical use.
期刊论文(0)
专著(0)
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会议论文
Oocyte-derived R-spondin2 as a Follicle Stimulating Hormone
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批准号:8526219
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资助金额:$18.92万
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财政年份:2012
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负责人:AARON JW HSUEH
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依托单位:
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批准号:8368062
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批准号:7964577
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批准号:7640438
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资助金额:$24.03万
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财政年份:2009
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负责人:AARON JW HSUEH
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依托单位:
Activation of dormant ovarian follicles
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批准号:7849497
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项目类别:
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资助金额:$20.04万
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财政年份:2009
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负责人:AARON JW HSUEH
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依托单位:
Identification of ligand signaling for the stem cell marker LGR5
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批准号:7632206
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资助金额:$19.75万
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财政年份:2008
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负责人:AARON JW HSUEH
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依托单位:
Identification of ligand signaling for the stem cell marker LGR5
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批准号:7510574
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项目类别:
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资助金额:$23.7万
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财政年份:2008
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负责人:AARON JW HSUEH
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依托单位:
Physiology of LGR7 and LGR8 in Gonadal Tissues
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批准号:6873661
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项目类别:
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资助金额:$28.81万
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财政年份:2003
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负责人:AARON JW HSUEH
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依托单位:
Physiology of LGR7 and LGR8 in Gonadal Tissues
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批准号:6745135
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项目类别:
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资助金额:$28.81万
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财政年份:2003
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负责人:AARON JW HSUEH
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依托单位:
Physiology of LGR7 and LGR8 in Gonadal Tissues
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批准号:7055339
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项目类别:
-
资助金额:$28.14万
-
财政年份:2003
-
负责人:AARON JW HSUEH
-
依托单位:
Physiology of LGR7 and LGR8 in Gonadal Tissues
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批准号:7224802
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项目类别:
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资助金额:$27.32万
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财政年份:2003
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负责人:AARON JW HSUEH
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依托单位:
Physiology of LGR7 and LGR8 in Gonadal Tissues
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批准号:6605276
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项目类别:
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资助金额:$28.45万
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财政年份:2003
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负责人:AARON JW HSUEH
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依托单位:
G Protein-Coupled Receptors with Leucine-Rich Repeats
-
批准号:6400133
-
项目类别:
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资助金额:$15.71万
-
财政年份:2001
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负责人:AARON JW HSUEH
-
依托单位:
G Protein-Coupled Receptors with Leucine-Rich Repeats
-
批准号:6517827
-
项目类别:
-
资助金额:$15.71万
-
财政年份:2001
-
负责人:AARON JW HSUEH
-
依托单位:
BIOACTIVE FSH AND REPRODUCTION
-
批准号:6682944
-
项目类别:
-
资助金额:$25.8万
-
财政年份:1997
-
负责人:AARON JW HSUEH
-
依托单位:
BIOACTIVE FSH AND REPRODUCTION
-
批准号:2471427
-
项目类别:
-
资助金额:$20.84万
-
财政年份:1997
-
负责人:AARON JW HSUEH
-
依托单位:
BIOACTIVE FSH AND REPRODUCTION
-
批准号:2888950
-
项目类别:
-
资助金额:$21.83万
-
财政年份:1997
-
负责人:AARON JW HSUEH
-
依托单位:
BIOACTIVE FSH AND REPRODUCTION
-
批准号:6387532
-
项目类别:
-
资助金额:$22.88万
-
财政年份:1997
-
负责人:AARON JW HSUEH
-
依托单位:
BIOACTIVE FSH AND REPRODUCTION
-
批准号:6406960
-
项目类别:
-
资助金额:$27.62万
-
财政年份:1997
-
负责人:AARON JW HSUEH
-
依托单位:
国内基金
海外基金
Inhibin B通过负反馈FSH介导头颅照射致远端生殖损伤的分子机制
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批准号:--
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项目类别:青年科学基金项目
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资助金额:30万元
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批准年份:2022
-
负责人:胡松玲
-
依托单位:
心肌细胞分泌的Inhibin通过作用于心肌成纤维细胞调控心肌纤维化的机制研究
-
批准号:82100302
-
项目类别:青年科学基金项目(C类)
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资助金额:30.0万元
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批准年份:2021
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负责人:贾鹏宇
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依托单位: