Team:Heidelberg/pages/Linker Screening

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=Introduction=
=Introduction=
Circularization is  a narrow path between gaining heat-stability and loosing function due to deformation.
Circularization is  a narrow path between gaining heat-stability and loosing function due to deformation.
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<p>The choice of the protein to perform the linker screen was constrained by different requirements. First, it needed to be easily and fast expressed in E.coli. We needed to be able to measure its functionality without purification and in an easy, fast, cheap and reliable way. It needed to be known for having a certain stability at high temperature with, at the same time, a loss of functionality so that the heat stabilization could be tested. Finally, the major constrain for the choise was the structure of the protein. First, we needed a cristal structure of the complete protein at high resolution. Second, the ends should be separated by a distance of 15 to 30 Angströms, so that the rigid linkers containing alpha helices would be relevant.</p>
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<p>Lysozymes are well characterized enzymes that are able to digest the peptidoglycans that form the bacterial wall. This process is performed by many different species for different applications, including antibacterial defense by plants and animals [[#Reference|[1]]]or bacterial penetration by viruses [[#Reference|[2]]]. On top, lysozyme is applied in different  fields of biotechnology and medicine. It is notably one of the most  important proteins in food preservation and is produced in the 100  tons scale a year. </p>
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The choice of the protein to perform the linker screen was constrained by different requirements. First, it needed to be easily and fast expressed in E.coli. We needed to be able to measure its functionality without purification and in an easy, fast, cheap and reliable way. It needed to be known for having a certain stability at high temperature with, at the same time, a loss of functionality so that the heat stabilization could be tested. Finally, the major constrain for the choise was the structure of the protein. First, we needed a cristal structure of the complete protein at high resolution. Second, the ends should be separated by a distance of 15 to 30 Angströms, so that the rigid linkers containing alpha helices would be relevant.
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<p>We anticipated that the lysozyme of the bacteriophage lambda could reasonably fulfill the requirements for our linker screen. </p>
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<p>Its crystal structure is known [[#Reference|[3]]] and the ends are 18 Angströms apart (fig.1). It  is easy to obtain: one can clone it from the bacteriophage lambda genome, and express it in E.coli. The fact that the overexpression of the enzyme eventually lyse the cells was not considered as a problem as long as enough enzyme would  be produced. Finally substrates to measure the enzymatic activity are commercially available.
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Lysozymes are well characterized enzymes that are able to digest the peptidoglycans that form the bacterial wall. This process is performed by many different species for different applications, including antibacterial defense by plants and animals [[#Reference|[1]]]or bacterial penetration by viruses [[#Reference|[2]]]. On top, lysozyme is applied in different  fields of biotechnology and medicine. It is notably one of the most  important proteins in food preservation and is produced in the 100  tons scale a year.  
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We anticipated that the lysozyme of the bacteriophage lambda could reasonably fulfill the requirements for our linker screen.  
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Its crystal structure is known [[#Reference|[3]]] and the ends are 18 Angströms apart (fig.1). It  is easy to obtain: one can clone it from the bacteriophage lambda genome, and express it in E.coli. The fact that the overexpression of the enzyme eventually lyse the cells was not considered as a problem as long as enough enzyme would  be produced. Finally substrates to measure the enzymatic activity are commercially available.
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===Main Results===
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We could clone and express the lysozyme of bacteriophage lambda and its fusion to different linkers (tab.1) chosen to calibrate our linker software.  We used lyophilized Micrococcus lysodeikticus as substrate to measure lysozyme activity and we established a heat shock assay to measure the heat-stability of the enzyme. We observed that while lysozyme shows a clear activity at 37°C, it is gradually lost when the enzyme is pretreated at higher temperatures up to 57°C. Thanks to our measurement of the kinetics of substrate processing, we could extract information on the amount of active enzyme at different heat shock temperature and with different linkers by [[http://2014.igem.org/Team:Heidelberg/Modeling#X|modeling]] this activity.
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The following figure shows the substrate processing measured from the decrease of optical density of the M. lysodeikticus  for the different temperatures of heat shock and the different linkers.
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=References=

Revision as of 10:03, 12 October 2014

We developed a modeling approach to design linkers that can circularize proteins and that may confer some rigidity in particular after heat shock. The general concept of the approach can be found in the [[1]] and the [[2]] sections The experimental work presented in this section has two main goals. The first one was testing the validity of the idea: Can rigid linkers with angles indeed provide heat stability to a protein better than flexible linkers? And the second one was to measure this stabilization depending on the properties of the linkers to calibrate the [Software]. As already seen in the software part, these properties are the total length of the linker, the angles between consecutive alpha helices, the regions that the linker passes and the distance from the proteins surface. As we had no a priori knowledge on the contribution of those different properties for the heat stability of the protein, we performed an extensive linker screening on the lambda phage lysozyme. The linkers checked were predicted to different groups by the software: Very good, somehow good, maybe working, bad and too short.

Introduction

Circularization is a narrow path between gaining heat-stability and loosing function due to deformation.

The choice of the protein to perform the linker screen was constrained by different requirements. First, it needed to be easily and fast expressed in E.coli. We needed to be able to measure its functionality without purification and in an easy, fast, cheap and reliable way. It needed to be known for having a certain stability at high temperature with, at the same time, a loss of functionality so that the heat stabilization could be tested. Finally, the major constrain for the choise was the structure of the protein. First, we needed a cristal structure of the complete protein at high resolution. Second, the ends should be separated by a distance of 15 to 30 Angströms, so that the rigid linkers containing alpha helices would be relevant.

Lysozymes are well characterized enzymes that are able to digest the peptidoglycans that form the bacterial wall. This process is performed by many different species for different applications, including antibacterial defense by plants and animals [1]or bacterial penetration by viruses [2]. On top, lysozyme is applied in different fields of biotechnology and medicine. It is notably one of the most important proteins in food preservation and is produced in the 100 tons scale a year. We anticipated that the lysozyme of the bacteriophage lambda could reasonably fulfill the requirements for our linker screen. Its crystal structure is known [3] and the ends are 18 Angströms apart (fig.1). It is easy to obtain: one can clone it from the bacteriophage lambda genome, and express it in E.coli. The fact that the overexpression of the enzyme eventually lyse the cells was not considered as a problem as long as enough enzyme would be produced. Finally substrates to measure the enzymatic activity are commercially available.

Main Results

We could clone and express the lysozyme of bacteriophage lambda and its fusion to different linkers (tab.1) chosen to calibrate our linker software. We used lyophilized Micrococcus lysodeikticus as substrate to measure lysozyme activity and we established a heat shock assay to measure the heat-stability of the enzyme. We observed that while lysozyme shows a clear activity at 37°C, it is gradually lost when the enzyme is pretreated at higher temperatures up to 57°C. Thanks to our measurement of the kinetics of substrate processing, we could extract information on the amount of active enzyme at different heat shock temperature and with different linkers by [[3]] this activity. The following figure shows the substrate processing measured from the decrease of optical density of the M. lysodeikticus for the different temperatures of heat shock and the different linkers.


References