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Structural Characterization of Ribonucleic Acids and Their Complexes by Negative-ion Mode Mass Spectrometry
Structural Characterization of Ribonucleic Acids and Their Complexes by Negative-ion Mode Mass Spectrometry

상세정보

자료유형  
 학위논문
Control Number  
0015000549
International Standard Book Number  
9780438126572
Dewey Decimal Classification Number  
540
Main Entry-Personal Name  
Ileka, Kevin M.
Publication, Distribution, etc. (Imprint  
[Sl] : University of Michigan, 2018
Publication, Distribution, etc. (Imprint  
Ann Arbor : ProQuest Dissertations & Theses, 2018
Physical Description  
146 p
General Note  
Source: Dissertation Abstracts International, Volume: 79-12(E), Section: B.
General Note  
Adviser: Kristina I. Hakansson.
Dissertation Note  
Thesis (Ph.D.)--University of Michigan, 2018.
Summary, Etc.  
요약Ribonucleic acids (RNAs) form complexes with deoxyribonucleic acids, proteins, other RNAs, and smaller ligands. Detailed knowledge of RNA interaction sites provides a basis for understanding functions. With limited analytical techniques availabl
Summary, Etc.  
요약Negative-ion electron capture dissociation (niECD) involves &sim
Summary, Etc.  
요약Electrospray ionization (ESI) of a model RNA hairpin from native-like (10 mM ammonium acetate) and methanol-containing (up to 50%) solvents resulted in identical charge state distributions, suggesting a minor methanol effect on overall conformat
Summary, Etc.  
요약Crosslinking techniques coupled with MS provide an alternative tool for identifying RNA interaction sites. We show that collisional activation can provide full sequence coverage of the RNA moiety within non-covalent RNA-peptide complexes
Summary, Etc.  
요약Microfluidics is a highly efficient technology for biological analysis. Microfluidic-type approaches, including nano-ESI and nano-LC, coupled with MS provide several advantages, e.g., limited sample consumption and enhanced sensitivity. In order
Summary, Etc.  
요약Overall, this dissertation describes the utility of MS (and its associated tools) for the study of RNA, RNA-small molecule, and RNA-protein complexes.
Subject Added Entry-Topical Term  
Molecular chemistry
Added Entry-Corporate Name  
University of Michigan Chemistry
Host Item Entry  
Dissertation Abstracts International. 79-12B(E).
Host Item Entry  
Dissertation Abstract International
Electronic Location and Access  
로그인을 한후 보실 수 있는 자료입니다.
Control Number  
joongbu:554045

MARC

 008190618s2018                                          c    eng  d
■001000015000549
■00520190102172830
■020    ▼a9780438126572
■035    ▼a(MiAaPQ)AAI10903051
■035    ▼a(MiAaPQ)umichrackham:001182
■040    ▼aMiAaPQ▼cMiAaPQ
■0820  ▼a540
■1001  ▼aIleka,  Kevin  M.
■24510▼aStructural  Characterization  of  Ribonucleic  Acids  and  Their  Complexes  by  Negative-ion  Mode  Mass  Spectrometry
■260    ▼a[Sl]▼bUniversity  of  Michigan▼c2018
■260  1▼aAnn  Arbor▼bProQuest  Dissertations  &  Theses▼c2018
■300    ▼a146  p
■500    ▼aSource:  Dissertation  Abstracts  International,  Volume:  79-12(E),  Section:  B.
■500    ▼aAdviser:  Kristina  I.  Hakansson.
■5021  ▼aThesis  (Ph.D.)--University  of  Michigan,  2018.
■520    ▼aRibonucleic  acids  (RNAs)  form  complexes  with  deoxyribonucleic  acids,  proteins,  other  RNAs,  and  smaller  ligands.  Detailed  knowledge  of  RNA  interaction  sites  provides  a  basis  for  understanding  functions.  With  limited  analytical  techniques  availabl
■520    ▼aNegative-ion  electron  capture  dissociation  (niECD)  involves  &sim
■520    ▼aElectrospray  ionization  (ESI)  of  a  model  RNA  hairpin  from  native-like  (10  mM  ammonium  acetate)  and  methanol-containing  (up  to  50%)  solvents  resulted  in  identical  charge  state  distributions,  suggesting  a  minor  methanol  effect  on  overall  conformat
■520    ▼aCrosslinking  techniques  coupled  with  MS  provide  an  alternative  tool  for  identifying  RNA  interaction  sites.  We  show  that  collisional  activation  can  provide  full  sequence  coverage  of  the  RNA  moiety  within  non-covalent  RNA-peptide  complexes
■520    ▼aMicrofluidics  is  a  highly  efficient  technology  for  biological  analysis.  Microfluidic-type  approaches,  including  nano-ESI  and  nano-LC,  coupled  with  MS  provide  several  advantages,  e.g.,  limited  sample  consumption  and  enhanced  sensitivity.  In  order
■520    ▼aOverall,  this  dissertation  describes  the  utility  of  MS  (and  its  associated  tools)  for  the  study  of  RNA,  RNA-small  molecule,  and  RNA-protein  complexes.
■590    ▼aSchool  code:  0127.
■650  4▼aMolecular  chemistry
■690    ▼a0431
■71020▼aUniversity  of  Michigan▼bChemistry.
■7730  ▼tDissertation  Abstracts  International▼g79-12B(E).
■773    ▼tDissertation  Abstract  International
■790    ▼a0127
■791    ▼aPh.D.
■792    ▼a2018
■793    ▼aEnglish
■85640▼uhttp://www.riss.kr/pdu/ddodLink.do?id=T15000549▼nKERIS
■980    ▼a201812▼f2019

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