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氧化铝富集糖肽的研究
  • ISSN号:0567-7351
  • 期刊名称:《化学学报》
  • 时间:0
  • 分类:Q513.2[生物学—生物化学]
  • 作者机构:[1]大连医科大学附属第二医院,大连116023, [2]中国科学院大连化学物理研究所中国科学院分离分析化学重点实验室,大连116023, [3]辽宁宇洁环保咨询有限公司,沈阳110000
  • 相关基金:国家高技术研究发展计划863计划(No.2012AA020203);国家自然科学基金(Nos.81171486,21105100);材料复合新技术国家重点实验室(武汉理工大学,2013-KF-8)开放基金资助
中文摘要:

糖基化蛋白对于生命体的生长发育,免疫调节,细胞识别粘附等具有重要意义,而异常的糖基化表达与风湿关节炎、肿瘤、阻塞性肺病等疾病密切相关.因此糖蛋白结构检测对于研究生命活动至关重要.由于在复杂样品中糖肽含量相对较少,加之非糖肽的离子抑制作用,使得糖肽的质谱检测有一定的挑战性.因此发展一种有效富集糖肽的方法是必要的.本实验中我们选用氧化铝对糖肽进行富集研究,并考察了影响氧化铝保留多肽的机理.我们利用氧化铝,从HRP酶解液中共获得16个糖肽,从IgG酶解液中共获得12个糖肽.与直接检测样品酶解液和经商品化材料Sepharose富集后再检测相比,检测到糖肽的个数增多.实验数据证明氧化铝富集糖肽具有较好的选择性和覆盖率.

英文摘要:

Protein glycosylation is significantly associated with cells cycle,immune regulation,cells recognition and cells adhesion.Aberrant glycosylation expression is involved in many diseases,such as rheumatoid arthritis,cancer,and chronic obstructive pulmonary disease.Thus,characterization of the protein glycosylation is very important to understand the life process.However,detection of glycopeptides is difficult by mass spectrometry because of the low concentration in complex sample and the suppressed signal by non-glycopeptides.Therefore,it is essential to explore an effective technique for glycopeptide enrichment.In this study,an alumina based-materials was used to selectively enrich glycopeptides.Firstly,we investigated the retention mechanism by changing the concentration of acetonitrile(ACN).With the decreased concentration of ACN,it was found that peptides were eluted according to their hydrophilicity.Moreover,most of the non-glycopeptides were eluted earlier than the glycopeptides in the high concentration of ACN fraction and the glycopeptides were found in the low concentration of ACN fraction.This result proved that hydrophilic interaction is one of the retention mechanisms for peptides retained by alumina.Secondly,we investigated the retention mechanism by changing the concentration of ammonium hydroxide.ACN were fixed at a high concentration and peptides were subsequently eluted with different concentration of ammonium hydroxide solution.At a low concentration of ammonium hydroxide solution,the peptides were no found.But at a high concentration of ammonium hydroxide solution,the glycopeptides and non-glycopeptides were eluted simultaneously.This proved that the ligand exchange is also one of the retention mechanisms,where the retention of the glycopeptides and non-glycopeptides showed no different under this mechanism.Based on the above mentioned results,the enrichment condition was optimized under the model of solid-phase extraction.High concentration of ACN mixed with a certain concentration of ammoni

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期刊信息
  • 《化学学报》
  • 北大核心期刊(2014版)
  • 主管单位:中国科学院
  • 主办单位:中国化学会 中国科学院上海有机化学研究所
  • 主编:周其林
  • 地址:上海市零陵路345号
  • 邮编:200032
  • 邮箱:hxxb@sioc.ac.cn
  • 电话:021-54925085
  • 国际标准刊号:ISSN:0567-7351
  • 国内统一刊号:ISSN:31-1320/O6
  • 邮发代号:4-209
  • 获奖情况:
  • 首届国家期刊奖,第二届国家期刊奖提名奖,中国期刊方阵“双高期刊”
  • 国内外数据库收录:
  • 俄罗斯文摘杂志,美国化学文摘(网络版),荷兰文摘与引文数据库,美国科学引文索引(扩展库),日本日本科学技术振兴机构数据库,中国中国科技核心期刊,中国北大核心期刊(2004版),中国北大核心期刊(2008版),中国北大核心期刊(2011版),中国北大核心期刊(2014版),英国英国皇家化学学会文摘,中国北大核心期刊(2000版)
  • 被引量:28694