Biomineralization mechanism and evolution of nano-structured habu snake venom fang
Biomineralization mechanism and evolution of nano-structured habu snake venom fang
批准号:
24651130
负责人:
OGAWA Tomohisa
金额:
$2.66万
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:
2012
资助国家:
日本
项目状态:
已结题
起止时间:
2012-04-01 至 2014-03-31
中文摘要
有毒动物不仅具有产毒腺,还具有注毒器官,如毒牙、毒囊等,可有效地向猎物注射毒液。 本研究采用蛋白质组学和转录组学相结合的方法,对黄绿原棘头蛇(Protobothrops flavoviridis,habu)毒牙基质蛋白的结构和性质进行了分析。 2D-PAGE显示20多个蛋白质点,等电点为4 ~ 5,分子量为25- 55 kDa,主要成分为Ⅰ型胶原。 此外,生物矿化相关的蛋白质,如骨调节蛋白,IMPG 2,牙本质基质蛋白1等,通过RNA测序分析从成牙组织的转录产物中鉴定。
英文摘要
Venomous animals have not only the venom-producing gland but also venome-injecting organs such as venom-loaded fangs and nematocyst for the efficient venome-injection to prey species. Although it is considered that the venom fang have evolved functionally from teeth, their biomineralization mechanisms are still unknown.In this study, to clarify the structure and properties of the matrix proteins from Protobothrops flavoviridis (habu) snake venom fangs were analysed by combined proteomic and transcriptomics analyses.Venom-loaded fangs were calcified with 50% formic acid, and their proteins were extracted by 8M urea. 2D-PAGE showed the more than 20 protein spots with the isoelectric point ranging 4 to 5 and molecular weight of 25-55kDa including type I collagen as a major component. Furthermore, the biomineralization related proteins such as osteomodulin, IMPG2, dentin matrix protein 1 etc. were identified from transcription products by RNA-seq analysis of fang-forming tissues.
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ヘビ毒筋壊死因子ホスホリパーゼA_2の2つの機能部位を介した筋壊死発現機構
蛇毒肌坏死因子磷脂酶A_2两个功能位点介导的肌坏死表达机制
DOI:
--
发表时间:
2013
期刊:
影响因子:
--
作者:
[Yoshimura S, Komatsu M, Kaku K, Hori M, Ogawa T, Muramoto K, Kazama T, Ito Y, Toriyama K, 小川智久, 飛嶋雄,村本光二,服部正策,大野素徳,小川智久, 安居宏実,速見卓也,村本光二,服部正策,大野素徳,小川智久]
通讯作者:
安居宏実,速見卓也,村本光二,服部正策,大野素徳,小川智久
Biomineralization of Pteria penguin pearl shell nacre regulated by matrix proteins homologous to the Jacalin-related lectin via their sugar binding abilities and phospholization
与 Jacalin 相关凝集素同源的基质蛋白通过糖结合能力和磷酸化调节珍珠贝珍珠贝珍珠层的生物矿化
DOI:
--
发表时间:
2013
期刊:
影响因子:
--
作者:
[T. Ogawa, T. Naganuma, S. Sakaue, K. Liu, S. Sato, K. Muramoto, M. Osada, K. Yoshimi]
通讯作者:
K. Yoshimi
マベ真珠バイオミネラリゼーションの分子機構と機能性材料への応用
马贝珠生物矿化分子机制及其在功能材料中的应用
DOI:
--
发表时间:
2013
期刊:
影响因子:
--
作者:
[Yoshimura S, Komatsu M, Kaku K, Hori M, Ogawa T, Muramoto K, Kazama T, Ito Y, Toriyama K, 小川智久]
通讯作者:
小川智久
DOI:
10.1271/bbb.130367
发表时间:
2013-09-01
期刊:
BIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY
影响因子:
1.6
作者:
[Yamamoto, Shintaro, Tomiyama, Mai, Muramoto, Koji]
通讯作者:
Muramoto, Koji
マベ真珠ジャカリン関連レクチンのバイオミネラリゼーション機能の解析 : 糖鎖およびリン酸化による制御
马贝珍珠jacalin相关凝集素的生物矿化功能分析:糖链和磷酸化的调节
DOI:
--
发表时间:
2012
期刊:
影响因子:
--
作者:
[T. Ogawa, T. Naganuma, S. Sakaue, K. Liu, S. Sato, K. Muramoto, M. Osada, K. Yoshimi, 飛嶋雄,村本光二,服部正策,大野素徳,小川智久, 安居宏実,村本光二,大野素徳,小川智久, 小川智久,佐藤紗保,坂上静香,永沼孝子,村本光二]
通讯作者:
小川智久,佐藤紗保,坂上静香,永沼孝子,村本光二
共 17 条
Molecular mechanism of aragonite crystal formation by proteins from Pteria penguin pearl shell, and its application to the development of functional materials
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批准号:20350073
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项目类别:Grant-in-Aid for Scientific Research (B)
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资助金额:$12.56万
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财政年份:2008
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负责人:OGAWA Tomohisa
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依托单位:
Clarification of Carbohydrate-Recognition Mechanisms of Gralectins which Evolved via Accelerated Substitution and Their Application for Biotechnology
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批准号:14360045
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项目类别:Grant-in-Aid for Scientific Research (B)
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资助金额:$9.34万
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财政年份:2002
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负责人:OGAWA Tomohisa
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依托单位: