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Oxidative Protein Folding in vitro: a Study of the Cooperation between Quiescin- sulfhydryl Oxidase and Protein Disulfide Isomerase Pumtiwitt C. Rancy and Colin Thorpe* Department of Chemistry and Biochemistry, University of Delaware Lingxi Jiang

Pumtiwitt C. Rancy and Colin Thorpe *

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Oxidative Protein Folding in vitro : a Study of the Cooperation between Quiescin -sulfhydryl Oxidase and Protein Disulfide Isomerase. Pumtiwitt C. Rancy and Colin Thorpe * Department of Chemistry and Biochemistry, University of Delaware. Lingxi Jiang. Oxidative protein folding. - PowerPoint PPT Presentation

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Page 1: Pumtiwitt  C.  Rancy and  Colin Thorpe *

Oxidative Protein Folding in vitro: a

Study of the Cooperation between

Quiescin-sulfhydryl Oxidase and

Protein Disulfide Isomerase

Pumtiwitt C. Rancy and Colin Thorpe*

Department of Chemistry and Biochemistry, University of Delaware

Lingxi Jiang

Page 2: Pumtiwitt  C.  Rancy and  Colin Thorpe *

Oxidative protein folding

• A process that is responsible for the formation of disulfide bonds between cysteine residues in proteins.

• Driving force: a redox reaction, in which electrons are passed between several proteins and finally to a terminal electron acceptor.

2 RSH + O2 → RS-SR + H2O2

• In eukaryotes, the process of oxidative protein folding occurs in the endoplasmatic reticulum (ER).

• The term "sulfhydryl oxidase" was introduced more than 50 years ago.

Page 3: Pumtiwitt  C.  Rancy and  Colin Thorpe *

Ero1 vs QSOX1 Two distinct flavin-linked sulfhydryl oxidase families: Ero1 and Quiescin-sulfhydryl oxidase QSOX1

protein disulfide isomerase (PDI): contains two CxxC redox-active disulfides (4 -SH equivalents upon reduction)

Page 4: Pumtiwitt  C.  Rancy and  Colin Thorpe *
Page 5: Pumtiwitt  C.  Rancy and  Colin Thorpe *

The present work

Widely-used model protein: pancreatic RNase, with 4

disulfides and 105 fully oxidized disulfide isomers.

A more complicated model: riboflavin binding protein (RfBP,

a protein with 9 disulfides and hence >34 million pairings for

the fully oxidized protein).

Quenching of riboflavin fluorescence upon binding to the

folded apoprotein allows continuous monitoring of oxidative

folding.

Page 6: Pumtiwitt  C.  Rancy and  Colin Thorpe *

PROCEDURES• Subcloning, Expression, and Purification of Human (gi

48735337) and Chicken (gi 30923135) PDI

• Preparation of reduced and oxidized proteins (PDI, RNase, RfBP)

• Monitoring QSOX-mediated thiol oxidation using DTNB

• Refolding of Rnase followed by hydrolysis of cyclic CMP

• Refolding of RfBP followed by fluorescence

• Calculation of redox state of a and a' domains of PDI in

equilibrium with glutathione redox buffer

Page 7: Pumtiwitt  C.  Rancy and  Colin Thorpe *

RESULTS

Human and avian PDI are poor substrates of avian QSOX1

Symbol QSOX/PDI

☐ Avian/human

✪ Avian/avian

⏏ Human/human

+× control

Page 8: Pumtiwitt  C.  Rancy and  Colin Thorpe *

Oxidative refolding of pancreatic RNase with QSOX, PDI and redox buffers

SymbolReduced RNase

incubated with …

reduced PDI, QSOX

⏏ QSOX

✪ reduced PDI, GSH, GSSG

GSH, GSSG

Page 9: Pumtiwitt  C.  Rancy and  Colin Thorpe *

Oxidative refolding of reduced riboflavin binding protein (RfBP)

Page 10: Pumtiwitt  C.  Rancy and  Colin Thorpe *
Page 11: Pumtiwitt  C.  Rancy and  Colin Thorpe *

Refolding of reduced RfBP in the absence of QSOX

SymbolReduced RfBP incubated with riboflavin in the presence of…

redox buffer of GSH/GSSG

⏏ redox buffer, reduced PDI

redox buffer, reduced PDI,

QSOX

QSOX, reduced PDI

Page 12: Pumtiwitt  C.  Rancy and  Colin Thorpe *

Oxidative refolding of reduced RfBP using PDI alone

Page 13: Pumtiwitt  C.  Rancy and  Colin Thorpe *

CONCLUSIONS

Whether oxidizing equivalents are

generated by QSOX, Ero1, or other cellular

oxidants, the universal additional

requirement for efficient oxidative folding is

reduced PDI.

Page 14: Pumtiwitt  C.  Rancy and  Colin Thorpe *

Our PDIs are quite similar~!