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Development of effective blood purification treatment method usingHSA bound toxic comnpodus designed bpyhase display tecnohlogy

Development of effective blood purification treatment method usingHSA bound toxic comnpodus designed bpyhase display tecnohlogy
利用HSA结合有毒化合物设计的bpyhase显示技术开发有效的血液净化治疗方法
批准号:
23659088
负责人:
OTAGIRI Masaki
金额:
$2.33万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Challenging Exploratory Research
财政年份:
2011
资助国家:
日本
项目状态:
已结题
起止时间:
2011 至 2012

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中文摘要
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英文摘要
This study was undertaken to design and evaluate recombinant albumin mutant( specially, domain II mutant)with high bilirubin (BR) binding affinity via phage display technology.The results obtained here identified the amino acid residues that interact carboxylatesof BR in HSA, and also produces HSA domain II mutants with high BR binding affinity. To our knowledge, this is the first finding on HSA mutant with enhanced binding affinity to BR. This approach could be applied to other HSA bound toxic compounds that responsible for the progression oifseadse and thereby it will pave the way for the development ofminimally invasive and low cost blood clarification method.
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DOI: --
发表时间: 2011
期刊:
影响因子: --
作者: [Hisakazu Komori, Masaki Otagiri, et al]
通讯作者: et al
Interaction between p-cresyl sulfate and indoxyl sulfate during body disposition can influence their serum free concentrations in chronic kidney disease
对甲酚硫酸盐和硫酸吲哚酚在身体处置过程中的相互作用会影响慢性肾病患者的血清游离浓度
DOI: --
发表时间: 2011
期刊:
影响因子: --
作者: [Hiroshi Watanabe, Masaki Otagiri, et al]
通讯作者: et al
Structural insights into differences in drug binding selectivity between two forms of human {alpha}1-acid glycoprotein genetic variants, the A and F1*S forms.
对两种形式的人类 {α}1-酸性糖蛋白遗传变体(A 和 F1*S 形式)之间药物结合选择性差异的结构见解。
DOI: --
发表时间: 2011
期刊: J Biol Chem. in press
影响因子: --
作者: [Nishi K, Ono T, Nakamura T, Fukunaga N, Izumi M, Watanabe H, Suenaga A, Maruyama T, Yamagata Y, Curry S, Otagiri M.]
通讯作者: Otagiri M.
DOI: --
发表时间: 2012
期刊:
影响因子: --
作者: [Kimura, H, 太田英伸]
通讯作者: 太田英伸
84
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