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Engineering Affinity-Based Sensing Systems for Continuous Biomolecular Monitoring
Engineering Affinity-Based Sensing Systems for Continuous Biomolecular Monitoring
Engineering Affinity-Based Sensing Systems for Continuous Biomolecular Monitoring

상세정보

자료유형  
 학위논문 서양
최종처리일시  
20260202105312
ISBN  
9798270228286
DDC  
543
저자명  
Flynn, Connor Daniel.
서명/저자  
Engineering Affinity-Based Sensing Systems for Continuous Biomolecular Monitoring
발행사항  
[Sl] : Northwestern University, 2025
발행사항  
Ann Arbor : ProQuest Dissertations & Theses, 2025
형태사항  
190 p
주기사항  
Source: Dissertations Abstracts International, Volume: 87-06, Section: B.
주기사항  
Advisor: Kelley, Shana O.
학위논문주기  
Thesis (Ph.D.)--Northwestern University, 2025.
초록/해제  
요약Continuous biomolecular monitoring remains among the most captivating and elusive goals of modern analytical science, with the potential to revolutionize both the understanding and treatment of human disease. However, despite decades of innovation in analyte recognition, sensor transduction, and material interfacing, glucose remains the only molecular target that can be continuously and reliably monitored in vivo. While glucose detection was perfected owing largely to its compatibility with enzymatic sensing, the reliance of other analytes on affinity-based recognition elements has introduced a host of challenges related to receptor reversibility, stability, and sensitivity. The development of molecular pendulum sensing offers a reagent less, electrochemical method for direct protein quantification that begins to address several of these limitations, though important challenges remain. In this thesis, the expansion and refinement of molecular pendulum-based sensing is explored with a particular focus on identifying design principles that enable continuous biomolecular analysis. A combination of electrochemical experimentation, biomolecular engineering, and computational analysis was used to investigate how factors such as pendulum probe composition, geometry, and environment can be harnessed to enhance sensitivity, improve sensor lifetime, and expand molecular recognition to new classes of targets. In addition, affinity-based recognition elements were explored for their compatibility, whether natural or engineered, with continuous biomolecular monitoring applications. Through these efforts, important relationships between molecular design, binding kinetics, redox behavior, and electrochemical modulation were uncovered, establishing a more generalizable framework for improved affinity-based sensing.
일반주제명  
Analytical chemistry
일반주제명  
Chemistry
일반주제명  
Biochemistry
일반주제명  
Chemical engineering
키워드  
Biosensing
키워드  
Continuous monitoring
키워드  
Electrochemistry
키워드  
Biomolecular engineering
키워드  
Biosensors
기타저자  
Northwestern University Chemistry
기본자료저록  
Dissertations Abstracts International. 87-06B.
전자적 위치 및 접속  
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MARC

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■1001  ▼aFlynn,  Connor  Daniel.
■24510▼aEngineering  Affinity-Based  Sensing  Systems  for  Continuous  Biomolecular  Monitoring
■260    ▼a[Sl]▼bNorthwestern  University▼c2025
■260  1▼aAnn  Arbor▼bProQuest  Dissertations  &  Theses▼c2025
■300    ▼a190  p
■500    ▼aSource:  Dissertations  Abstracts  International,  Volume:  87-06,  Section:  B.
■500    ▼aAdvisor:  Kelley,  Shana  O.
■5021  ▼aThesis  (Ph.D.)--Northwestern  University,  2025.
■520    ▼aContinuous  biomolecular  monitoring  remains  among  the  most  captivating  and  elusive  goals  of  modern  analytical  science,  with  the  potential  to  revolutionize  both  the  understanding  and  treatment  of  human  disease.  However,  despite  decades  of  innovation  in  analyte  recognition,  sensor  transduction,  and  material  interfacing,  glucose  remains  the  only  molecular  target  that  can  be  continuously  and  reliably  monitored  in  vivo.  While  glucose  detection  was  perfected  owing  largely  to  its  compatibility  with  enzymatic  sensing,  the  reliance  of  other  analytes  on  affinity-based  recognition  elements  has  introduced  a  host  of  challenges  related  to  receptor  reversibility,  stability,  and  sensitivity.  The  development  of  molecular  pendulum  sensing  offers  a  reagent  less,  electrochemical  method  for  direct  protein  quantification  that  begins  to  address  several  of  these  limitations,  though  important  challenges  remain.  In  this  thesis,  the  expansion  and  refinement  of  molecular  pendulum-based  sensing  is  explored  with  a  particular  focus  on  identifying  design  principles  that  enable  continuous  biomolecular  analysis.  A  combination  of  electrochemical  experimentation,  biomolecular  engineering,  and  computational  analysis  was  used  to  investigate  how  factors  such  as  pendulum  probe  composition,  geometry,  and  environment  can  be  harnessed  to  enhance  sensitivity,  improve  sensor  lifetime,  and  expand  molecular  recognition  to  new  classes  of  targets.  In  addition,  affinity-based  recognition  elements  were  explored  for  their  compatibility,  whether  natural  or  engineered,  with  continuous  biomolecular  monitoring  applications.  Through  these  efforts,  important  relationships  between  molecular  design,  binding  kinetics,  redox  behavior,  and  electrochemical  modulation  were  uncovered,  establishing  a  more  generalizable  framework  for  improved  affinity-based  sensing.
■590    ▼aSchool  code:  0163.
■650  4▼aAnalytical  chemistry
■650  4▼aChemistry
■650  4▼aBiochemistry
■650  4▼aChemical  engineering
■653    ▼aBiosensing
■653    ▼aContinuous  monitoring
■653    ▼aElectrochemistry
■653    ▼aBiomolecular  engineering
■653    ▼aBiosensors
■690    ▼a0486
■690    ▼a0487
■690    ▼a0542
■690    ▼a0485
■71020▼aNorthwestern  University▼bChemistry.
■7730  ▼tDissertations  Abstracts  International▼g87-06B.
■790    ▼a0163
■791    ▼aPh.D.
■792    ▼a2025
■793    ▼aEnglish
■85640▼uhttp://www.riss.kr/pdu/ddodLink.do?id=T17360157▼nKERIS▼z이  자료의  원문은  한국교육학술정보원에서  제공합니다.

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