Search for an endogenous collagenase in chicken endochondral bone matrix vesicles.

The Penn dental journal Pub Date : 2001-01-01
D Chen, E E Golub
{"title":"Search for an endogenous collagenase in chicken endochondral bone matrix vesicles.","authors":"D Chen,&nbsp;E E Golub","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>While isolating matrix vesicles from avian endochondral bone, collagenase activity was discovered unexpectedly. The question was raised whether this collagenase activity was endogenous or if it was due to the bacterial collagenase used to release the matrix vesicles from bone. In related experiments done, collagen partially degraded by collagenase mineralized better than undegraded collagen. This study would then attempt to show if an endogenous collagenase is found, whether it facilitates collagen mineralization by allowing better access for matrix vesicles by the \"nicking\" of collagen. From this two-month study evidence was found that an endogenous collagenase as well as a gelatinase was present on matrix vesicles. SDS gel electrophoresis and zymography were used to determine the presence of collagenases in purified matrix vesicle fractions. Western blots with antibodies to bacterial collagenase, matrix metallo-proteinases 13 (MMP-13), an endogenous collagenase, and MMP-2, an endogenous gelatinase, were also done to determine the presence of an endogenous collagenase. Another facet was added to this study to determine if contamination by exogenous collagenase during matrix vesicle isolation could be removed. From the final Western blots done, it was verified that even after exhaustive washings of the column and centrifugation, purified matrix vesicles contained contaminating bacterial collagenase. Due to the research completed, the matrix vesicle isolation protocol was changed from using bacterial collagenase to a trypsin isolation method to prevent any exogenous collagenase contamination.</p>","PeriodicalId":76715,"journal":{"name":"The Penn dental journal","volume":"101 ","pages":"12-3, 32"},"PeriodicalIF":0.0000,"publicationDate":"2001-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Penn dental journal","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

While isolating matrix vesicles from avian endochondral bone, collagenase activity was discovered unexpectedly. The question was raised whether this collagenase activity was endogenous or if it was due to the bacterial collagenase used to release the matrix vesicles from bone. In related experiments done, collagen partially degraded by collagenase mineralized better than undegraded collagen. This study would then attempt to show if an endogenous collagenase is found, whether it facilitates collagen mineralization by allowing better access for matrix vesicles by the "nicking" of collagen. From this two-month study evidence was found that an endogenous collagenase as well as a gelatinase was present on matrix vesicles. SDS gel electrophoresis and zymography were used to determine the presence of collagenases in purified matrix vesicle fractions. Western blots with antibodies to bacterial collagenase, matrix metallo-proteinases 13 (MMP-13), an endogenous collagenase, and MMP-2, an endogenous gelatinase, were also done to determine the presence of an endogenous collagenase. Another facet was added to this study to determine if contamination by exogenous collagenase during matrix vesicle isolation could be removed. From the final Western blots done, it was verified that even after exhaustive washings of the column and centrifugation, purified matrix vesicles contained contaminating bacterial collagenase. Due to the research completed, the matrix vesicle isolation protocol was changed from using bacterial collagenase to a trypsin isolation method to prevent any exogenous collagenase contamination.

鸡软骨内骨基质囊泡内源性胶原酶的研究。
从禽软骨内骨中分离基质囊泡时,意外地发现了胶原酶活性。问题是这种胶原酶活性是内源性的,还是由于细菌胶原酶用于从骨中释放基质囊泡。在相关实验中,被胶原酶部分降解的胶原比未降解的胶原矿化得更好。这项研究将试图证明是否发现了内源性胶原酶,是否通过胶原蛋白的“缺口”使基质囊泡更好地进入,从而促进胶原蛋白矿化。从这两个月的研究证据发现,内源性胶原酶以及明胶酶存在于基质囊泡。采用SDS凝胶电泳和酶谱法测定纯化的基质囊泡组分中胶原酶的存在。用细菌胶原酶抗体、内源性胶原酶基质金属蛋白酶13 (MMP-13)抗体和内源性明胶酶MMP-2抗体进行Western blots检测,以确定内源性胶原酶的存在。本研究的另一个方面是确定基质囊泡分离过程中外源性胶原酶的污染是否可以去除。从最后完成的Western blots中,证实即使在彻底清洗柱和离心后,纯化的基质囊泡也含有污染的细菌胶原酶。由于本研究的完成,为了防止外源性胶原酶污染,将基质囊泡分离方法从使用细菌胶原酶改为使用胰蛋白酶分离方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信