Determinants of antimicrobial activity and salt-resistance of defensin
Determinants of antimicrobial activity and salt-resistance of defensin
批准号:
20790803
负责人:
SHIRAFUJI Yoshinori
金额:
$2.58万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Young Scientists (B)
财政年份:
2008
资助国家:
日本
项目状态:
已结题
起止时间:
2008 至 2009
中文摘要
人β防御素(HBD)-3对革兰氏阴性菌和革兰氏阳性菌均有较强的抗盐抗菌活性,而其他HBD只对革兰氏阴性菌有抗菌活性,在盐存在下其抗菌活性减弱。我们推测,这些特征是由于HBD-3的COOH-末端有两个精氨酸残基,而其他HBD-3没有涉及到。为了进行研究,我们命名了HBD-3的两个重组突变体:Desr HBD-3,其中这两个精氨酸残基从HBD-3中删除,NRR-HBD-3中,这两个精氨酸残基从COOH端移动到NH2端,并对它们的抗菌活性和耐盐性进行了研究。结果表明,为了保持HBD-3的活性和耐盐性,这两个精氨酸残基需要存在于COOH-末端。
英文摘要
Human β-defensin (HBD) -3 has potent and salt-resistant antimicrobial activity against both gram-negativeand gram positive bacteria and this activity, while other HBDs possess antimicrobial activity against only gram-negative strains and it is attenuated under salt existence. We hypothesized that these characteristics are due to two arginine residues in the COOH-terminal of HBD-3 which is not involved in other HBD-3. To investigate, we designated two recombinant mutants of HBD-3; desR HBD-3 in which these two arginine residues were deleted from HBD-3 and NRR-HBD-3 in which these two arginine residues were shifted from COOH-terminal to NH2-terminal and esxamined their antimicrobial activities and salt-resistance. The results showed that these two argine residues are required to exist in the COOH-terminal in order to maintain the activity and salt-resistance of HBD-3.
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Elevated expression of Paneth cell CRS4C in ileitis-prone SAMP1/YitFc mice: regional distribution, subcellular localization, and mechanism of action.
易患回肠炎的 SAMP1/YitFc 小鼠中潘氏细胞 CRS4C 表达升高:区域分布、亚细胞定位和作用机制。
DOI:
10.1074/jbc.m109.083220
发表时间:
2010
期刊:
The Journal of biological chemistry
影响因子:
--
作者:
[Shanahan,MichaelT, Vidrich,Alda, Shirafuji,Yoshinori, Dubois,ClaireL, Henschen-Edman,Agnes, Hagen,SusanJ, Cohn,StevenM, Ouellette,AndréJ]
通讯作者:
Ouellette,AndréJ
アトピー性皮膚炎病変部に浸潤する炎症細胞による抗菌ペプチドの発現
浸润特应性皮炎皮损的炎症细胞表达抗菌肽
DOI:
--
发表时间:
2008
期刊:
影响因子:
--
作者:
[Yoshinori Shirafuji, Yoko Sakagami, Takashi Oono, Keiji Iwatsuki, Yoshinori Shirafuji, 大野貴司]
通讯作者:
大野貴司
デフェンシン活性化のメカニズム
防御素激活机制
DOI:
--
发表时间:
2008
期刊:
影响因子:
--
作者:
[Yoko Sakagami, Yoshinori Shirafuji, Takahi Oono, Keiji Iwatsuki, 白藤宜紀]
通讯作者:
白藤宜紀
Antimicrobial activity of human beta-defensin-3 against metallo beta lactamase producing Pseudomonas
人β-防御素-3对产生金属β内酰胺酶的假单胞菌的抗菌活性
DOI:
--
发表时间:
2008
期刊:
影响因子:
--
作者:
[Yoshinori Shirafuji, Yoko Sakagami, Takashi Oono, Keiji Iwatsuki]
通讯作者:
Keiji Iwatsuki
Two Arginine residues in the COOH-terminal of human beta-defensin-3 affect broad antimicrobial activities and salt-resistance
人 β-防御素 3 COOH 末端的两个精氨酸残基影响广泛的抗菌活性和耐盐性
DOI:
--
发表时间:
2009
期刊:
影响因子:
--
作者:
[Shanahan, M. T、. Vidrich, A. 、Shirafuji, Y., 他5名, 阪上陽子]
通讯作者:
阪上陽子
共 7 条
Structural determinant of Humanβ-defensin-3 to stimulate cytokine/chemokine secretion
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批准号:22791075
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项目类别:Grant-in-Aid for Young Scientists (B)
-
资助金额:$2.5万
-
财政年份:2010
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负责人:SHIRAFUJI Yoshinori
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依托单位:
海外基金