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鉴别一种可被蛋白衣壳包裹的短肽

摘要第3-7页
Abstract第7-8页
Chapter 1 Introduction第11-25页
    1.1 Natural encapsulation using protein capsids第11-13页
    1.2 Engineered Capsids as containers第13-18页
    1.3 Lumazine synthase第18-22页
    1.4 Aim of this thesis第22-25页
Chapter 2 Materials and Methods第25-57页
    2.1 Ecoli cells and plasmids第25页
    2.2 Reagents第25-27页
    2.3 Primers第27-28页
    2.4 Instruments第28页
    2.5 Plasmid construction第28-33页
        2.5.1 Materials for plasmid of GFP variants第28-30页
        2.5.2 Methods第30-33页
    2.6 Protein production and purification第33-39页
        2.6.1 Materials第33-34页
        2.6.2 Methods第34-39页
    2.7 SDS-PAGE第39-41页
        2.7.1 Materials for SDS-PAGE第39页
        2.7.2 Method for SDS-PAGE第39-40页
        2.7.3 Yield detection by SDS-PAGE第40页
        2.7.4 Measurement of protein concentration第40-41页
    2.8 Analytical size-exclusion chromatography第41页
    2.9 Fluorescence spectroscopy第41-43页
    2.10 UV detection for loading yield第43-44页
    2.11 MS detection of co-purifying proteins第44页
    2.12 The characterization of BsLS with His6 tag第44-47页
        2.12.1 Site directed mutagenesis第44-45页
        2.12.2 BsLS-H6 protein production and purification第45-47页
        2.12.3 SDS-PAGE analysis for BsLS-H6 capsid loading第47页
    2.13 ELISA Detection of GFP11第47-48页
    2.14 Western blotting analysis for Abrin A-HA-BsRS11第48-49页
    2.15 Guest release from the capsid第49-50页
    2.16 TEM第50-51页
    2.17 Attempts at capsid loading in vitro第51-52页
    2.18 AaLS-switch-pH capsid become pentamer第52页
    2.19 AaLS-switch-pH pentamer go back to capsid第52页
    2.20 Phage display第52-57页
Chapter 3 Results第57-85页
    3.1 Design of fusion proteins第57-58页
    3.2 Analysis of capsid-guest complexes第58-80页
        3.2.1 SEC and A280 analysis第58-60页
        3.2.2 Fluorescence spectroscopy第60-65页
        3.2.3 SDS-PAGE analysis第65-70页
        3.2.4 UV detection for loading yield第70-71页
        3.2.5 Detection of GFP by ELISA第71页
        3.2.6 The specificity and generality of the encapsulation system第71-74页
        3.2.7 Guest release from the capsid第74-76页
        3.2.8 TEM第76-78页
        3.2.9 Attempted in vitro loading第78-80页
    3.3 Selection of encapsulation peptide tags for AaLS第80-85页
        3.3.1 Confirming of AaLS-switch-pH第80-81页
        3.3.2 Phage display selection round第81-85页
Chapter 4 Discussion第85-99页
    4.1 The loading yield of other engineering capsids第85页
    4.2 The encapsulation yield of GFPs第85-86页
    4.3 The specificity and generality of the encapsulation system第86-87页
    4.4 The analysis of 24 LS and RS第87-95页
    4.5 The mild release condition of BsLS capsid第95-96页
    4.6 conclusion and future work第96-99页
References第99-107页
Publication in scientific research第107-109页
Acknowledgements第109页

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