【摘 要】
:
Organophosphorus agents(OPs)like sarin,VX,or soman could inhibit acetylcholinesterase activity and cause poisoning.OPs could bind many proteins,such as butyrylcholinesterase and albumin,and the adduct
【机 构】
:
State Key Laboratory of NBC Protection for Civilian.Changping District,Beijing 102205 China
【出 处】
:
第八届国际分子模拟与信息技术应用学术会议
论文部分内容阅读
Organophosphorus agents(OPs)like sarin,VX,or soman could inhibit acetylcholinesterase activity and cause poisoning.OPs could bind many proteins,such as butyrylcholinesterase and albumin,and the adducts formed could identify the exposure.In this paper,we studied human transferrin,which was one of the proteins that could be labeled by OPs.Pure human transferrin was incubated with an overdose of organophosphorus agents,including sarin,soman,VX,tabun,cyclosarin,ethyl tabun,and propyl tabun,and then additional OPs was removed thro ugh dialysis.Trypsin was used to cleave the OP-treated proteins and Q Exactive liquid chromatography randem mass spectrometry(Q Exactive LC-MS/MS)was used to identify them.The present study set out to accomplish two goals.The first goal was to find a good method for identifying multiple binding sites on a given protein through Q Exactive LC-MS/MS.The second goal was to investigate the labeled peptides when transferrin was incubated with a numerous molar excess of OPs.Results showed that tyrosine,lysine,and serine formed covalent bonds with OPs.Twenty OP-labeled sites were found: ten tyrosine sites(including two reported sites),seven lysine sites,and three serine sites.Characteristic fragments for labeled-tyrosine and labeled-lysine adducts were summarized in detail.In conclusion,the method by Q Exactive LC-MS/MS using in this present work is a good way to diagnose exposure to OPs accurately when the binding sites of OPs are uncertain.Novel modified peptides and the characteristic ions found in this work could help investigators assess exposure to OPs.
其他文献
用自发结晶的方法获得了第一个带有F-离子的碱土金属铍硼酸盐Ca3Be6B5O16F.Ca3Be6B5O16F的结构框架是由相互连接的[Be6B3O16]和[BO3]基团所构成,[CaO7F]扭曲的多面体处于骨架的空隙当中.[Be6B3O16]是在硼酸盐中首次发现.紫外-可见-近红外漫反射光谱表明,其紫外截止边于200nm,并且得到了第一性原理的证明.热分析揭示Ca3Be6B5O16F属于非同成分熔
A novel series of 1,3-diphenyl-2-propen-1-one(chalcone)derivatives was synthesized by a simple,ecofriendly,and efficient Claisen-Schmidt condensation reaction and used as precursors for the synthesis
BLyS antagonists have become the therapeutic reagents in the treatment of autoimmune disorders.BLyS binding peptides and their Fc fusion proteins may be altemative BLyS antagonists in Such application
A series of 4-alkoxyquinazoline derivatives containing 1,3,4-oxadiaxole scafifold have been designed and synthesized,and their inhibitory activities were also tested against A549,MCF-7 and Hela.Of the
Predicting target-ligand interactions is a critical task of chemogenomics and plays a key role in virtual drug discovery.Moreover,it is important to lake insights into the molecular recognition mechan
Macrocyclic polyketides,biosynthesized by modular polyketide synthases(PKSs),have been developed successfully into generation-by-generation pharmaceuticals for numerous therapeutic areas.A great effor
The 2014-2015 Ebola virus(EBOV)outbreak in West Africa highlighted the urgent need for specific therapeutic interventions for infected patients.The human-mouse chimeric monoclonal antibody(mAb)cocktai
LARP7.a member of the La-related proteins(LARPs),shares a conserved La module comprising the La-motif(LAM)and the RNA-recognition motif(RRM1),binding exclusively to the non-coding RNA 7SK.LARP7 is a c
Liver X receptor α(LXRα)plays an important role in the cholesterol metabolism process,and LXRα activation can reduce atherosclerosis.In the present study,using an LXRα-GAL4 luciferase reporter screeni
Objectives: Drug-resistant Mycobacterium tuberculosis poses a great threat to human health.Tyrosyl-tRNA synthetase(TyrRS)is one of the aminoacyl tRNA synthetases that catalyse the attachment of amino