CONTROL OF PROTEIN NUCLEATION AND CRYSTALLITE GROWTH
CONTROL OF PROTEIN NUCLEATION AND CRYSTALLITE GROWTH
批准号:
6139242
负责人:
PETER G VEKILOV
金额:
$14.38万
依托单位国家:
美国
项目类别:
财政年份:
1998
资助国家:
美国
项目状态:
已结题
起止时间:
1998-01-01 至 2001-12-31
中文摘要
提出研究的目的是获得定量的
英文摘要
The objective of the proposed research is to obtain quantitative
understanding of protein nucleation and post-nucleation growth of small
protein crystals (crystallites) in order to: (a) improve crystallization
protocols yielding crystals of a structural perfection that matches
state-of-the-art X-ray diffraction techniques used in protein
structure/function studies and rational drug design; (b) achieve narrow
crystallite size distributions, which are essential for steady sustained
release of pharmaceutical protein preparations, such as insulin; and (c)
find means to regulate protein crystallization in vivo, e.g., the
formation of hemoglobin C crystals in red blood cells. The specific
aims to be pursued using four model globular proteins are: 1) Obtain
insight into the fundamental mechanisms of protein crystal nucleation
through studies of the dependencies of the nucleation rate on protein
concentration and solution supersaturation. 2) Define and quantify the
effects of: (i) soluble additives, biospecific for each protein, in
concentrations representative of those commonly occurring in
crystallizing protein solutions; and (ii) particulates with known size
and concentration. 3) Based on the insight obtained under Aims 1) and
2), demonstrate that protein crystal nucleation can be controlled to
achieve improvements in the areas (a)-(c) above. The basic hypothesis
underlying this work is that nucleation concepts derived for inorganic
systems, subject to modifications for differences in solution
interactions and molecular kinetics, can provide guidance in protein
nucleation. A key element of the proposed investigation is a novel
automated multi-cell microscopy technique for protein nucleation
studies. This technique allows direct measurements of the nucleation
rates and quantitative correlations to the nucleation conditions. Unlike
previous protein nucleation studies, these nucleation rate
determinations are not based on any assumptions about the molecular
interactions in the crystallization solution.
期刊论文(9)
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DOI:
10.1006/jmbi.2000.4171
发表时间:
2000-11
期刊:
Journal of molecular biology
影响因子:
5.6
作者:
[S. Yau;D. Petsev;B. R. Thomas;P. Vekilov]
通讯作者:
S. Yau;D. Petsev;B. R. Thomas;P. Vekilov
Hemoglobin fluorescence.
血红蛋白荧光。
DOI:
10.1385/1-59259-373-9:133
发表时间:
2003
期刊:
Methods in molecular medicine.
影响因子:
--
作者:
[Hirsch,RhodaElison]
通讯作者:
Hirsch,RhodaElison
DOI:
10.1021/cg1011633
发表时间:
2010-11-15
期刊:
CRYSTAL GROWTH & DESIGN
影响因子:
3.8
作者:
[Vekilov, Peter G.]
通讯作者:
Vekilov, Peter G.
Intermolecular interactions, nucleation, and thermodynamics of crystallization of hemoglobin C.
血红蛋白 C 的分子间相互作用、成核和结晶热力学。
DOI:
10.1016/s0006-3495(02)75238-7
发表时间:
2002
期刊:
Biophysical journal
影响因子:
3.4
作者:
[Vekilov,PeterG, Feeling-Taylor,AngelaR, Petsev,DimiterN, Galkin,Oleg, Nagel,RonaldL, Hirsch,RhodaElison]
通讯作者:
Hirsch,RhodaElison
Molecular mechanisms of microheterogeneity‐induced defect formation in ferritin crystallization
铁蛋白结晶中微异质性诱导缺陷形成的分子机制
DOI:
10.1002/prot.1047
发表时间:
2001
期刊:
Proteins: Structure
影响因子:
--
作者:
[S. Yau, B. R. Thomas, O. Galkin, O. Gliko, P. Vekilov]
通讯作者:
P. Vekilov
Hematin crystallization in Plasmodium parasites
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批准号:9169162
-
项目类别:
-
资助金额:$20.28万
-
财政年份:2016
-
负责人:PETER G VEKILOV
-
依托单位:
CONTROL OF PROTEIN NUCLEATION AND CRYSTALLITE GROWTH
-
批准号:2857926
-
项目类别:
-
资助金额:$16.55万
-
财政年份:1998
-
负责人:PETER G VEKILOV
-
依托单位:
CONTROL OF PROTEIN NUCLEATION AND CRYSTALLITE GROWTH
-
批准号:2469023
-
项目类别:
-
资助金额:$16.33万
-
财政年份:1998
-
负责人:PETER G VEKILOV
-
依托单位:
国内基金
海外基金
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基于超声空化选择性降解瘤内Ferritin增效三阴性乳腺癌铁死亡的基础研
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资助金额:--
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批准号:82270591
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项目类别:面上项目
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资助金额:52万元
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批准年份:2022
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负责人:李鹏
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依托单位:
Ferritin家族在帽贝牙齿生物矿化中的功能研究
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穿透支原体 Ferritin 蛋白的免疫保护功能及机制研究
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批准年份:2022
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负责人:何玲
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依托单位:
Ferritin介导细胞铁死亡调节血管钙化的机制研究
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批准号:
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资助金额:10.0万元
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批准年份:2021
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蓝藻发菜抗低温胁迫中一个含ferritin-like结构域蛋白Csrnf1的作用及其机理研究
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