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2003 中研院之行

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2003 中研院之行. 趙裕展老師實驗室. 趙裕展老師. Expression of Spike Immunodominant Domains Using Baculovirus Expression Vector System. 蔡聖輝. Introduction. SARS-CoV. S - Spike protein: receptor binding, cell fusion, major antigen E - Envelope protein: small, envelope-associated protein - PowerPoint PPT Presentation

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Page 1: 2003 中研院之行

20032003 中研院之行中研院之行趙裕展老師實驗室趙裕展老師實驗室

趙裕展老師趙裕展老師

Page 2: 2003 中研院之行

Expression of Spike Immunodominant Domains Expression of Spike Immunodominant Domains Using Baculovirus Expression Vector SystemUsing Baculovirus Expression Vector System

蔡聖輝蔡聖輝

Page 3: 2003 中研院之行

IntroductionIntroduction

Page 4: 2003 中研院之行

S - Spike protein: receptor binding, cell fusion, major antigen E - Envelope protein: small, envelope-associated protein

M - Membrane protein: transmembrane - budding & envelope formation

SARS: Severe Acute Respiratory SyndromBEVS: Baculovirus Expression Vector System

SARS-CoVSARS-CoV

Page 5: 2003 中研院之行

IntroductionIntroduction

Spike protein is a membrane protein with a large extracellular domain,

and is a major inducer of protective immune responses

200 a.a.

450-657 equivalent to 417-547 of HCoV-229E

Spike, SARS-CoV

coil-coiledoligomerization domain547

763966

Page 6: 2003 中研院之行

1.Preparation of vABhRpS1.Preparation of vABhRpS547547HH66

pABhRpS547H6

Linearize virus DNA

co-transfection

recombinantdead

purify

(End-point dilution)

Page 7: 2003 中研院之行

End-point dilutionEnd-point dilution

Wt : 999

Recombinant virus : 1

Dilution 10x

Wt : 98

Recombinant virus : 2

Wt : 100

Recombinant virus : 0

Wt : 100

Recombinant virus : 0

Wt : 980

Recombinant virus : 20

1000

1

50

1

Page 8: 2003 中研院之行

End-point dilutionEnd-point dilution

Wt : 980

Recombinant virus : 20

Dilution 100x

Wt : 7

Recombinant virus : 3

Wt : 9

Recombinant virus : 1

Wt : 700

Recombinant virus : 300

50

1

Wt : 10

Recombinant virus : 0

7

3

Page 9: 2003 中研院之行

End-point dilutionEnd-point dilution

Wt : 700

Recombinant virus : 300

Dilution 1000x

Recombinant virus : 1

Wt : 1

Recombinant virus : 1000

Wt : 1

100%

7

3

Page 10: 2003 中研院之行

Preparation of vABhRpSPreparation of vABhRpS547547HH66

pABhRpS547H6

Linearize virus DNA

co-transfection

recombinantdead

purify

amplify

test titer

4.21X108 pfu/ml

Page 11: 2003 中研院之行

Identification of expression of SIdentification of expression of S547547

mar

ker

cont

rol

med

ium

S547(glycosylation) 70

med

ium

+ + -vABhRpSvABhRpS547547HH66

kDa

55

90

1 2 3

- +PNGase A

sample

Western blotting

antibodies against His-tag

S547

glycosylation

S547= 60.784 kDa(theoretically)

His-tagSignal peptide

Page 12: 2003 中研院之行

epithelial cells in upper respiratory tractMucosal inductive sites

M

Antigen-processing

sIgA

Receptor

2.Construction of pABhRpS2.Construction of pABhRpS763763rBHrBH66

pABhRpS pABhRpS966966rBHrBH66

ricinB

RicinB binds the sugar moiety, which, in turn, leading to internalization by M-cells.M-cell is able to process antigen, resulting in the activation of mucosal immune response. And the hallmark of mucosal immunity is the formation of sIgA.

Page 13: 2003 中研院之行

ricinB

Spike

Since ricinB is able to target specific M-cells, any polypeptide (in our case, spike protein) fused to ricinB could be targeted and internalized into M-cells, resulting in development of mucosal immune response against SARS insults.

Page 14: 2003 中研院之行

S763

S966

PCR

S763

S966

Cla I Stu I EcoR I

S763

S966

Cla I Stu I EcoR I

pBSrB

ricinB

Pac I Sac I

Cla I EcoR I

H6

pBSrBSxxx

ricinB

Pac I Sac I

EcoR I

H6

Sxxx

Cla I Stu I

procedureprocedure

Page 15: 2003 中研院之行

pBSSxxxrB

ricinB

Pac I Sac I

H6

Sxxx

Stu I

digestionLigation with pABhRpX

p-polh

pABhRpS763rBH6

pABhRpS966rBH6

Sxxx

Page 16: 2003 中研院之行

Summary

1.Successful construction of recombinant virus vABhRpSvABhRpS547547HH66..

2. Another four viruses which contain 2. Another four viruses which contain S763 and S966 are currently under construction.