Team:Heidelberg/pages/Circularization

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However, even the most truncated yet functional form of DNMT1 (872 aa) is much larger than GFP or MBP and its termini are far away from each other. Therefore, it is necessary to put a large linker between the termini. A long flexible linker would probably not be able to significantly enhance thermostability, since the termini would not be locked in one position.  
However, even the most truncated yet functional form of DNMT1 (872 aa) is much larger than GFP or MBP and its termini are far away from each other. Therefore, it is necessary to put a large linker between the termini. A long flexible linker would probably not be able to significantly enhance thermostability, since the termini would not be locked in one position.  
So we came up with the idea to design rigid linkers with angles [[Team:Heidelberg/Modeling/Linker_Modeling]] and developed a software to generate linkers for any protein [[Team:Heidelberg/Software/Linker_Software]]. We circularized lambda lysozyme in order to test and calibrate our linker model [[Team:Heidelberg/Project/Linker_Screening]]. Circular lambda lysozymes with 9 different linkers were screened for thermostability.  
So we came up with the idea to design rigid linkers with angles [[Team:Heidelberg/Modeling/Linker_Modeling]] and developed a software to generate linkers for any protein [[Team:Heidelberg/Software/Linker_Software]]. We circularized lambda lysozyme in order to test and calibrate our linker model [[Team:Heidelberg/Project/Linker_Screening]]. Circular lambda lysozymes with 9 different linkers were screened for thermostability.  
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===What could be done?===
 
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===How does circularization increase thermostability?===
===How does circularization increase thermostability?===
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Backbone cyclization of proteins increases the thermostability of a protein in a similar way to the introduction of disulfide bridges. Either way, a covalent linkage is introduced that decreases the entropy of the unfolded state of the protein [[#References|[12]]]. This principle has already been shown in 1956 in the context of fibrous proteins with covalent linkages [[#References|[3]]]. A short explanation of "the entropy of the unfolded state is decreased": an unfolded linear polypeptide can move around a lot, each angle between the peptide bonds can have any possible state. If the polypeptide is circular, the state of those angles is much more restricted. Consequently, this unfolded state is less likely to occur, resulting in a higher therostability.  
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Backbone cyclization of proteins increases the thermostability of a protein in a similar way to the introduction of disulfide bridges. Either way, a covalent linkage is introduced that decreases the entropy of the unfolded state of the protein [[#References|[12]]]. This principle has already been shown in 1956 in the context of fibrous proteins with covalent linkages [[#References|[3]]]. A short explanation of "the entropy of the unfolded state is decreased": an unfolded linear polypeptide can move around a lot, each angle between the peptide bonds can have any possible state. If the polypeptide is circular, the state of those angles is much more restricted. Consequently, this unfolded state is less likely to occur, resulting in a higher thermostability.  
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Another factor that might improve thermostability is the fixation of the termini. They are usually flexible and thus a possible starting point of the denaturation process [12]. Especially if no linker is needed or a rigid linker is used, this should cause an additional increase of thermostability.  
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Another factor that might improve thermostability is the fixation of the termini. They are usually flexible and thus a possible starting point of the denaturation process [[#References|[12]]]. Especially if the termini are close together or a rigid linker is used to join them [linkermodel], this should cause an additional increase of thermostability.  
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===What could be done?===
===References===
===References===

Revision as of 16:26, 14 October 2014

Contents

Circularization

Introduction

Proteins normally appear in nature with two ends, the N-terminal amino and the C-terminal carboxylic groups. By linking those two ends, it is possible circularize these proteins and introduce interesting properties. Circular proteins can be superior to linear proteins in terms of thermostability [1][2][3], stability against chemical denaturation [4] and exopeptidase resistance [2][4], while the biological function of he linear counterpart is conserved [5]. Improving thermostability of enzymes is an essential aspect for industrial applications [5]. Indeed, in many applications, those enzymes are required to work at temperatures that would normally cause denaturation [6]. Other recombinant proteins, for example enzymes used in laboratories, are required to be as stable as possible at moderate temperatures [6]. Moreover, a circular backbone can improve in vivo stability of therapeutical proteins and peptides [5]. Our circularization tools allow easy expression of circular proteins in e. coli. Choose a protein you want to circularize and use our [toolbox guide]!

Circular proteins in nature

Due to their extraordinary features, circular proteins have emerged independently in different organisms. Those proteins are rather small (<79 amino acids) and most often them are additionally stabilized by disulfide bonds [7]. A pharmaceutically active cyclic peptide from a plant, katala B1, has been used by African women to accelerate childbirth and was obtained by boiling the dry plant leaves, demonstrating its considerable thermostability [8]. This cyclic peptide belongs to the large family of cyclotides, which might have a great potential in drug design [7]. Most of the circular peptides found in nature have a defense function. Rhesus θ-defensin-1, found in rhesus macaque leukocytes, is a highly potent antibiotic peptide [9]. Cyclosporine, a small circular peptide from fungi, is able to suppress the human immune system and thus important for transplant surgery [7]. Importantly, naturally occurring circularization of more complex and larger proteins have not yet been described. Considering the benefit that one can expect from improved protein stability, we anticipated that developing tools to circularize proteins would be of great help for the scientific and industrial communities.

What has been done?

For that part, you may want to cite the review: Biological synthesis of circular polypeptides, Aboye and Camarero, JBC, 2012

Using [split inteins] or [sortase], it is possible to cirularize linear proteins. The most important proteins that were circularized using split inteins are dihydrofolate reductase [1] and GFP [4]. Those proteins are rather small and their termini are in close proximity. Both circular dihydrofolate reductase and GFP showed enhanced resistance against proteases and denaturation. The largest protein circular protein yet is maltose-binding protein (MBP) (395 aa) from E. coli [10]. However, stability was not tested in this case. A GFP variant was also circularized in vitro using sortase. In this case, faster recovery of fluorescence after denaturation was observed in comparison with a linear control [11].


What have we done?

Our interest for protein circularization originated from our ambitious idea to create a thermostable DNA methyltransferase that could be included in a polymerase chain reaction (PCR) to transfer the methylation state of the original DNA to the product. Knowing the importance of DNA methylation in gene expression regulation, such a PCR assay would be a revolution for epigenetics. In practice, we aimed at circularizing DNA (cytosine-5)-methyltransferase 1 (DNMT1) Team:Heidelberg/Project/PCR_2.0. If DNMT1 and the cofactor S-adenosyl methionine (SAM) could simply be added to a conventional PCR reaction, DNA could be amplified without losing methylation.. Consequently, we planned to circularize DNMT1 in order to improve its thermostability as much as possible. We used GFP to test both split intein and sortase circularization. We successfully circularized GFP in vivo using a preliminary split intein-based circularization construct Team:Heidelberg/Toolbox/Circularization_Constructs. However, even the most truncated yet functional form of DNMT1 (872 aa) is much larger than GFP or MBP and its termini are far away from each other. Therefore, it is necessary to put a large linker between the termini. A long flexible linker would probably not be able to significantly enhance thermostability, since the termini would not be locked in one position. So we came up with the idea to design rigid linkers with angles Team:Heidelberg/Modeling/Linker_Modeling and developed a software to generate linkers for any protein Team:Heidelberg/Software/Linker_Software. We circularized lambda lysozyme in order to test and calibrate our linker model Team:Heidelberg/Project/Linker_Screening. Circular lambda lysozymes with 9 different linkers were screened for thermostability.


How does it work?

 our constructs, warum super und notwendig


How does circularization increase thermostability?

Backbone cyclization of proteins increases the thermostability of a protein in a similar way to the introduction of disulfide bridges. Either way, a covalent linkage is introduced that decreases the entropy of the unfolded state of the protein [12]. This principle has already been shown in 1956 in the context of fibrous proteins with covalent linkages [3]. A short explanation of "the entropy of the unfolded state is decreased": an unfolded linear polypeptide can move around a lot, each angle between the peptide bonds can have any possible state. If the polypeptide is circular, the state of those angles is much more restricted. Consequently, this unfolded state is less likely to occur, resulting in a higher thermostability.

Another factor that might improve thermostability is the fixation of the termini. They are usually flexible and thus a possible starting point of the denaturation process [12]. Especially if the termini are close together or a rigid linker is used to join them [linkermodel], this should cause an additional increase of thermostability.

What could be done?

References

[1] Scott, C. P., Abel-Santos, E., Wall, M., Wahnon, D. C. & Benkovic, S. J. Production of cyclic peptides and proteins in vivo. Proc. Natl. Acad. Sci. 96, 13638–13643 (1999).

[2] Iwai, H. & Plückthun, A. Circular beta-lactamase: stability enhancement by cyclizing the backbone. FEBS Lett. 459, 166–72 (1999).

[3] Flory, J. & Yol, S. Theory of Elastic Mechanisms in Fibrous Proteins. 715, 5222–5235 (1956)

[4] Iwai, H., Lingel, a & Pluckthun, a. Cyclic green fluorescent protein produced in vivo using an artificially split PI-PfuI intein from Pyrococcus furiosus. J. Biol. Chem. 276, 16548–54 (2001).

[5] Trabi, M. & Craik, D. J. Circular proteins--no end in sight. Trends Biochem. Sci. 27, 132–8 (2002).

[6] Biology, S. Factors increasing protein thermostability. 1–41 (2002).

[7] Craik, D. J. Chemistry. Seamless proteins tie up their loose ends. Science 311, 1563–4 (2006).

[8] A, P. K. B. et al. Elucidation of the Primary and Three-Dimensional Structure of the Uterotonic. 4147–4158 (1995).

[9] Tang, Y. A Cyclic Antimicrobial Peptide Produced in Primate Leukocytes by the Ligation of Two Truncated -Defensins. Science (80-. ). 286, 498–502 (1999).

[10] Evans, T. C. Protein trans-Splicing and Cyclization by a Naturally Split Intein from the dnaE Gene of Synechocystis Species PCC6803. J. Biol. Chem. 275, 9091–9094 (2000).

[11] Antos, J. M. et al. A straight path to circular proteins. J. Biol. Chem. 284, 16028–36 (2009).

[12] Vieille, C. & Zeikus, G. J. Hyperthermophilic enzymes: sources, uses, and molecular mechanisms for thermostability. Microbiol. Mol. Biol. Rev. 65, 1–43 (2001).