博碩士論文 105384606 詳細資訊

以作者查詢圖書館館藏 以作者查詢臺灣博碩士 以作者查詢全國書目 勘誤回報 、線上人數:14 、訪客IP:
姓名 武高恩(VU CAO AN)  查詢紙本館藏   畢業系所 化學工程與材料工程學系
論文名稱 利用核適體作為訊號放大器於矽奈米線場效電晶體免疫感測器對生物標記物進行定量分析
(Aptamer as Signal Amplifier for Biomarker Quantification by Silicon Nanowire Field-Effect Transistor Immunosensors)
★ 類澱粉胜肽聚集行為之電腦模擬★ 溶解度參數計算及量測於HPLC純化胜肽程序之最佳化研究
★ 利用恆溫滴定微卡計量測蛋白質分子於溶液中之第二維里係數與自我聚集之行為★ 利用SPRi探討中性DNA探針相較於一般DNA探針在低鹽雜交環境下之優勢
★ 矽奈米線場效電晶體多點之核酸檢測研究★ 使用不帶電中性核酸探針於矽奈米線場效電晶體檢測去氧核醣核酸與微核醣核酸之研究
★ 運用nDNA 修飾引子於PCR及qPCR平台以提升專一性之研究★ 設計中性DNA引子及探針以提升PCR與qPCR專一性之研究
★ 使用中性不帶電去氧核醣核酸探針於矽奈米線場效電晶體檢測微核醣核酸之研究★ 使用不帶電中性核酸探針於原位雜交技術檢測微核醣核酸之研究
★ 設計不帶電中性核酸探針於矽奈米線場效電晶體來改善富含GC鹼基核醣核酸之檢測專一性★ 合成5’-MeNPOC-2’-deoxynucleoside p-methoxy phosphoramidite以作為應用於原位合成之新穎性中性核苷酸之研究
★ 立體紙基外泌體核酸萃取裝置應用於檢測不同微環境下癌細胞所釋放之外泌體與外泌體微小核醣核酸之表現量★ 利用抗原結合區段之抗體片段探針於矽奈米線場效電晶體來改善抗原檢測濃度極限之研究
★ 利用表面電漿共振影像儀驗證最適化之抗非專一性吸附場效電晶體表面於血清環境下之免疫測定★ 使用混合自組裝單層膜於矽奈米線場效電晶體檢測微小核醣核酸之研究
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摘要(中) 為了對疾病進行早期診斷,需要一個高靈敏度的檢測技術來檢測在生物樣品中極低濃度的生物標記物。矽奈米線場效電晶體因為其對多種目標物擁有高靈敏、免標定、即時檢測等優勢,已經被證明為一個有力的醫學診斷工具。但是,由於德拜長度屏蔽效應的影響以及非專一性吸附的干擾,使用奈米線場效電晶體生物傳感器來定量在生理環境下極低濃度的蛋白質生物標記物會受到嚴重的阻礙。本研究將會提供一個方法,透過使用核適體作為訊號放大器在矽奈米線場效電晶體之免疫測定檢測法,可以提高矽奈米線場效電晶體對生物標記物檢測能力,並且將之應用在β-澱粉樣蛋白(1-42)的定量檢測以進行對阿茲罕默症的早期診斷。
而後,這種方法被用於(3-氨基丙基)三乙氧基矽烷修飾和混合的自組裝單層修飾的矽奈米線場效電晶體生物傳感器上,對在150 mM BTP和人類血清這些具高離子強度和嚴重干擾的環境中稀釋不同濃度之β-澱粉樣蛋白進行定量分析。在兩種表面改質方式中皆是固定抗β-澱粉樣蛋白(1-42)之鼠源抗體在矽奈米線上,前者是用於三明治免疫測定法檢測β-澱粉樣蛋白;而後者是於矽奈米線上使用混和自組裝單層膜(組成: 矽氧烷-聚乙二醇-胺基和矽氧烷-聚乙二醇-醇基)進行表面改質。R18 核適體成功地用作這兩種改質方式之生物傳感器的信號放大器,由R18引起的電訊號變化量隨著生物樣品中β-澱粉樣蛋白(1-42)濃度的升高而增加,我們可以依此測定在150 mM BTP和人類血清中的β-澱粉樣蛋白(1-42)。實驗結果中共有3條檢量線,顯示了檢測到的β-澱粉樣蛋白(1-42)濃度與適體增強信號之間具有良好的線性關係。 由兩種免疫傳感器建立的三個定量範圍都非常符合Langmuir等溫吸附線模型,並且根據經驗數據計算的它們各自的Ka值(結合親和力)都在抗體-抗原結合親和力範圍內。在兩種改質方法中,尤其建議使用混和自組裝單層膜來修飾矽奈米線場效電晶體生物感測器,此方式可以在人類血清環境中測定100 fg/mL ~100 pg/mL的β-澱粉樣蛋白(1-42) ,計算檢量線的p值可以進一步證明數據有很高的顯著性。與最近的β-澱粉樣蛋白檢測技術相比,本研究可以檢測到的100 fg/ mL為最低的檢測極限濃度,並且獲得的定量範圍涵蓋了阿茲罕默症的早期診斷所需的β-澱粉樣蛋白濃度範圍。因此,本論文中描述的方法對應用於阿茲罕默症的早期診斷具有相當大的潛力,甚至可能可以在阿茲罕默症發展的更初期進行診斷,並且此檢測技術也可以應用在血液樣本中其他的生物標記物的極低濃度定量檢測。
摘要(英) Early-stage diagnosis plays an essential role in identifying diseases for proper treatment and therapy. However, it requires ultra-sensitive techniques to recognize biomarkers, which are associated with and alerts of various diseases, at ultra-low concentrations in bio-samples. Silicon nanowire field-effect transistor (SiNWFET) biosensors has been demonstrated as a powerful tool in diagnosis because it can yield high sensitivity for label-free and real-time detection of plentiful molecules. Nevertheless, determining protein biomarkers by SiNWFET immunosensors at ultra-low levels in physiological environments is severely hindered due to the limitation of screening effect and interference of non-specific bio-species. This thesis presents a strategy for protein sensing on SiNWFETs with aptamer as signal amplifier and apply it for protein biomarker quantification by SiNWFET immunosensors with Amyloid β 1-42 (Aβ 1-42), a biomarker for early-stage diagnosis of Alzheimer disease (AD), as a case study.
Initially, aptamer as signal enhancement for protein sensing by SiNWFET transducers are investigated via direct and sandwich immunoassays. The direct type was implemented by anchoring Hexahistidine on SiNWFET surface to be recognized by its respective rabbit immunoglobulin G (IgG) whereas the sandwich type was developed by immobilizing mouse antibodies on the sensing channels to capture Aβ 1-42 following with rabbit IgG. Both types of the sensors were then incubated with R18, an RNA aptamer specifically targeting rabbit IgG. Empirical results reveal that electrical variation produced from both direct and sandwich immunoassays is stabilized and remarkably amplified after incubating with R18 despite of inconsistent signal recorded in both models after detecting the corresponding proteins.
Subsequently, this approach is exploited for APTES-modified SiNWFET and mSAM-modified SiNWFET immunosensors (mSAM: mixed self-assembled monolayers) to quantify AB 1-42 at different concentrations in 150 mM Bis-Tris propane (BTP) and human serum (HS). The former are the ones used in sandwich immunoassay of Aβ 1-42 whereas the latter are developed from the NW surface modified with mSAMs of silane-PEG-NH2 and silane-PEG-OH. Aptamer as signal amplifier is successfully applied for both fabricated sensors to determine Aβ 1-42 in 150 mM BTP and HS with three calibration lines presenting well-linear relationship between detected concentrations of Aβ 1-42 and enhanced signal by aptamer. The linear ranges achieved by two kinds of immunosensors are well-fitted with Langmuir adsorption model and their Ka values (binding affinity), calculated from empirical data, are within the range of antibody-antigen binding affinity. Especially, the suggested solution exhibits an outstanding performance in combination with mSAM-SiNWFET immunosensors to quantify Aβ 1-42 in HS at level down to 100 fg/mL within a linear range of 100 fg/mL – 100 pg/mL, accredited the significance by p value. 100 fg/mL is the lowest limit of detection (LOD) in comparison with the most up-to-date sensing technologies for Aβ 1-42 and the linear range obtained covers the required range of Aβ 1-42 content for early-stage diagnosis of AD. The strategy described in this dissertation is therefore applicable for early-stage diagnosis of AD as well as potential for determining other biomarkers with ultra-low concentration in blood.
關鍵字(中) ★ 場效應晶體管生物傳感器
★ 適體
★ 兔抗體
★ Amyloid β 1-42
★ 信號增強
★ 免疫測定
關鍵字(英) ★ Field-Effect Transistor Biosensor
★ Aptamer
★ Rabbit Antibody
★ Amyloid β 1-42
★ Signal Enhancement
★ Immunoassay
論文目次 摘要 i
Abstract iv
Acknowledgements vi
Table of Contents vii
List of Figures x
List of Tables xv
Chapter 1: Introduction 1
1.1 Motivations 1
1.2 Objectives 4
1.3 Structure 5
Chapter 2: Research Background and Literature Review 7
2.1 SiNWFET Biosensors 7
2.2 Debye Length 12
2.3 Aptamers 15
2.4 Dementia and AD 19
2.5 Fouling Resistance for SiNWFET Immunosensors 27
Chapter 3: Materials & Methods 30
3.1 Materials 30
3.1.1 Chemicals 30
3.1.2 Apparatuses and instruments 31
3.2 Fabrication of SiNWFET Immunosensors 31
3.2.1 Preparation of 6xHis-immobilized SiNWFET immunosensors 31
3.2.2 Preparation of APTES-modified SiNWFET immunosensors (IgG1-immobilized SiNWFET immunosensors) 33
3.2.3 Preparation of mSAM-modified SiNWFET immunosensors 34
3.3 Performance of Biosensing and Signal Enhancing 35
3.3.1 Direct immunoassay and signal enhancing of 6xHis-immobilized SiNWFET imunosensors in 150 mM BTP 35
3.3.2 Sandwich immunoassay and signal enhancing of APTES-modified SiNWFET immunosensors (IgG1-immobilized SiNWFET immunosensors) 36
3.3.3 Detection of Aβ 1-42 in HS by mSAM-modified SiNWFET immunosensors and signal amplification by R18 aptamer 38
3.4 Data Analysis 40
Chapter 4: Electrical Responses of Direct and Sandwich Immunoassays by SiNWFET and Signal Enhancement by RNA Aptamer 41
4.1 Direct Immunoassay of Hexahistidine on SiNWFET and Signal Amplification by RNA Aptamer 41
4.2 Sandwich Immunoassay of Aβ 1-42 on SiNWFET and Signal Amplification by RNA Aptamer 44
4.3 Discussions on Aptamer as Signal Amplifier for SiNWFET Immunosensors 46
4.4 Summary 50
Chapter 5: Signal Enhancement from RNA Aptamer Improves Biomarker Quantification by SiNWFET Immunosensors 51
5.1 Amplified Signal from RNA Aptamer for Quantifying Aβ 1-42 in 150 mM BTP by APTES-modified SiNWFET Immunosensors 52
5.2 Amplified Signal from RNA Aptamer for Quantifying Aβ 1-42 in HS by APTES-modified SiNWFET Immunosensors 53
5.3 Amplified Signal from RNA Aptamer Improves Quantifying Aβ 1-42 in HS by mSAM-modified SiNWFET Immunosensors 55
5.4 Langmuir Adsorption Model in Further Analysis on Signal Enhancement of Aptamer for Aβ 1-42 Quantification by SiNWFET Immunosensors 58
5.5 Review and Discussions on Recent Aβ 1-42 Sensing Technologies 59
5.6 Summary 62
Chapter 6: Concluding Remarks and Future Prospects of Aptamers in FET Biosensors 63
6.1 Conclusions 63
6.2 Contributions 65
6.3 Future Prospects of Aptamers in FET Biosensors 66
Bibliographies 68
Appendixes 95
參考文獻 Bibliographies

[1] G.-J. Zhang and Y. Ning, "Silicon nanowire biosensor and its applications in disease diagnostics: a review," Anal. Chim. Acta, vol. 749, pp. 1-15, 2012.
[2] L. Syedmoradi, A. Ahmadi, M. L. Norton, and K. Omidfar, "A review on nanomaterial-based field effect transistor technology for biomarker detection," Microchim. Acta, vol. 186, no. 11, p. 739, 2019.
[3] K.-I. Chen, B.-R. Li, and Y.-T. Chen, "Silicon nanowire field-effect transistor-based biosensors for biomedical diagnosis and cellular recording investigation," Nano Today, vol. 6, no. 2, pp. 131-154, 2011.
[4] K. Blennow, H. Hampel, M. Weiner, and H. Zetterberg, "Cerebrospinal fluid and plasma biomarkers in Alzheimer disease," Nat. Rev. Neurol., vol. 6, no. 3, pp. 131-144, 2010.
[5] N. L. Rosi and C. A. Mirkin, "Nanostructures in biodiagnostics," Chem. Rev., vol. 105, no. 4, pp. 1547-1562, 2005.
[6] A. Poghossian and M. J. Schöning, "Label‐Free Sensing of Biomolecules with Field‐Effect Devices for Clinical Applications," Electroanalysis, vol. 26, no. 6, pp. 1197-1213, 2014.
[7] W. Zhou, X. Dai, and C. M. Lieber, "Advances in nanowire bioelectronics," Rep. Prog. Phys., vol. 80, no. 1, p. 016701, 2016.
[8] S. Liu and X. Guo, "Carbon nanomaterials field-effect-transistor-based biosensors," NPG Asia Mater., vol. 4, no. 8, pp. e23-e23, 2012.
[9] I. M. Feigel, H. Vedala, and A. Star, "Biosensors based on one-dimensional nanostructures," J. Mater. Chem., vol. 21, no. 25, pp. 8940-8954, 2011.
[10] S. Roy and Z. Gao, "Nanostructure-based electrical biosensors," Nano Today, vol. 4, no. 4, pp. 318-334, 2009.
[11] K. B. Cederquist and S. O. Kelley, "Nanostructured biomolecular detectors: pushing performance at the nanoscale," Curr. Opin. Chem. Biol., vol. 16, no. 3-4, pp. 415-421, 2012.
[12] F. P. Zamborini, L. Bao, and R. Dasari, "Nanoparticles in measurement science," Anal. Chem., vol. 84, no. 2, pp. 541-576, 2012.
[13] M. O. Noor and U. J. Krull, "Silicon nanowires as field-effect transducers for biosensor development: A review," Anal. Chim. Acta, vol. 825, pp. 1-25, 2014.
[14] Y. Cui and C. M. Lieber, "Functional nanoscale electronic devices assembled using silicon nanowire building blocks," Science, vol. 291, no. 5505, pp. 851-853, 2001.
[15] Y. Cui, L. J. Lauhon, M. S. Gudiksen, J. Wang, and C. M. Lieber, "Diameter-controlled synthesis of single-crystal silicon nanowires," Appl. Phys. Lett., vol. 78, no. 15, pp. 2214-2216, 2001.
[16] Y. Cui, Q. Wei, H. Park, and C. M. Lieber, "Nanowire nanosensors for highly sensitive and selective detection of biological and chemical species," Science, vol. 293, no. 5533, pp. 1289-1292, 2001.
[17] F. Patolsky, G. Zheng, and C. M. Lieber, "Fabrication of silicon nanowire devices for ultrasensitive, label-free, real-time detection of biological and chemical species," Nat. Protoc., vol. 1, no. 4, p. 1711, 2006.
[18] C.-A. Vu and W.-Y. Chen, "Field-effect transistor biosensors for biomedical applications: recent advances and future prospects," Sensors, vol. 19, no. 19, p. 4214, 2019.
[19] E. Stern et al., "Label-free immunodetection with CMOS-compatible semiconducting nanowires," Nature, vol. 445, no. 7127, pp. 519-522, 2007.
[20] S. Cheng et al., "Field effect transistor biosensor using antigen binding fragment for detecting tumor marker in human serum," Materials, vol. 7, no. 4, pp. 2490-2500, 2014.
[21] G. Zheng, F. Patolsky, Y. Cui, W. U. Wang, and C. M. Lieber, "Multiplexed electrical detection of cancer markers with nanowire sensor arrays," Nat. Biotechnol., vol. 23, no. 10, pp. 1294-1301, 2005.
[22] J.-i. Hahm and C. M. Lieber, "Direct ultrasensitive electrical detection of DNA and DNA sequence variations using nanowire nanosensors," Nano Lett., vol. 4, no. 1, pp. 51-54, 2004.
[23] Z. Li, Y. Chen, X. Li, T. Kamins, K. Nauka, and R. S. Williams, "Sequence-specific label-free DNA sensors based on silicon nanowires," Nano Lett., vol. 4, no. 2, pp. 245-247, 2004.
[24] A. Gao et al., "Silicon-nanowire-based CMOS-compatible field-effect transistor nanosensors for ultrasensitive electrical detection of nucleic acids," Nano Lett., vol. 11, no. 9, pp. 3974-3978, 2011.
[25] A. Gao et al., "Enhanced sensing of nucleic acids with silicon nanowire field effect transistor biosensors," Nano Lett., vol. 12, no. 10, pp. 5262-5268, 2012.
[26] G.-J. Zhang et al., "DNA sensing by silicon nanowire: charge layer distance dependence," Nano Lett., vol. 8, no. 4, pp. 1066-1070, 2008.
[27] W.-Y. Chen, H.-C. Chen, Y.-S. Yang, C.-J. Huang, H. W.-H. Chan, and W.-P. Hu, "Improved DNA detection by utilizing electrically neutral DNA probe in field-effect transistor measurements as evidenced by surface plasmon resonance imaging," Biosens. Bioelectron., vol. 41, pp. 795-801, 2013.
[28] F. Patolsky, G. Zheng, O. Hayden, M. Lakadamyali, X. Zhuang, and C. M. Lieber, "Electrical detection of single viruses," Proc. Natl. Acad. Sci. U. S. A., vol. 101, no. 39, pp. 14017-14022, 2004.
[29] F. Shen et al., "Rapid flu diagnosis using silicon nanowire sensor," Nano Lett., vol. 12, no. 7, pp. 3722-3730, 2012.
[30] W. U. Wang, C. Chen, K.-h. Lin, Y. Fang, and C. M. Lieber, "Label-free detection of small-molecule–protein interactions by using nanowire nanosensors," Proc. Natl. Acad. Sci. U. S. A., vol. 102, no. 9, pp. 3208-3212, 2005.
[31] R. Miao et al., "Silicon nanowire-based fluorescent nanosensor for complexed Cu2+ and its bioapplications," Nano Lett., vol. 14, no. 6, pp. 3124-3129, 2014.
[32] N. Shehada, G. Brönstrup, K. Funka, S. Christiansen, M. Leja, and H. Haick, "Ultrasensitive silicon nanowire for real-world gas sensing: noninvasive diagnosis of cancer from breath volatolome," Nano Lett., vol. 15, no. 2, pp. 1288-1295, 2015.
[33] J. F. Fennell Jr et al., "Nanowire chemical/biological sensors: Status and a roadmap for the future," Angew. Chem., vol. 55, no. 4, pp. 1266-1281, 2016.
[34] Z. Iskierko, K. Noworyta, and P. S. Sharma, "Molecular recognition by synthetic receptors: Application in field-effect transistor based chemosensing," Biosens. Bioelectron., vol. 109, pp. 50-62, 2018.
[35] A. C. M. De Moraes and L. T. Kubota, "Recent trends in field-effect transistors-based immunosensors," Chemosensors, vol. 4, no. 4, p. 20, 2016.
[36] E. Stern, R. Wagner, F. J. Sigworth, R. Breaker, T. M. Fahmy, and M. A. Reed, "Importance of the Debye screening length on nanowire field effect transistor sensors," Nano Lett., vol. 7, no. 11, pp. 3405-3409, 2007.
[37] R. Elnathan et al., "Biorecognition layer engineering: overcoming screening limitations of nanowire-based FET devices," Nano Lett., vol. 12, no. 10, pp. 5245-5254, 2012.
[38] N. Gao, W. Zhou, X. Jiang, G. Hong, T.-M. Fu, and C. M. Lieber, "General strategy for biodetection in high ionic strength solutions using transistor-based nanoelectronic sensors," Nano Lett., vol. 15, no. 3, pp. 2143-2148, 2015.
[39] L. De Vico et al., "Predicting and rationalizing the effect of surface charge distribution and orientation on nano-wire based FET bio-sensors," Nanoscale, vol. 3, no. 9, pp. 3635-3640, 2011.
[40] C.-A. Vu, W.-P. Hu, Y.-S. Yang, H. W.-H. Chan, and W.-Y. Chen, "Signal Enhancement of Silicon Nanowire Field-Effect Transistor Immunosensors by RNA Aptamer," ACS Omega, vol. 4, no. 12, pp. 14765-14771, 2019.
[41] E. Stern et al., "Label-free biomarker detection from whole blood," Nat. Nanotechnol., vol. 5, no. 2, pp. 138-142, 2010.
[42] B. Duthey, "Background paper 6.11: Alzheimer Disease and Other Dementias," in "Priority Medicines for Europe and the World "A Public Health Approach to Innovation"
指導教授 陳文逸(CHEN WEN YIH) 審核日期 2020-8-19
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