Team:SVCE CHENNAI/Description

Lactoshield - SVCE_CHENNAI Lactoshield - SVCE_CHENNAI

Lactoshield - SVCE_CHENNAI Lactoshield - SVCE_CHENNAI

In-silico Results


Computers play a vital role in any project. Biotechnology is no exception. Everything that we know today about biotech, we owe to bioinformatics. When it plays such a vital role in biological studies, it would be really prudent to exploit it to understand our projects further.

Part Enhancement 1 : cjBlue,green chromoprotein


Insilico analysis was done to construct a 3D model for this part. The sequence for this part was obtained from the iGEM registry and submitted to SWISS MODEL .The protein with the highest sequence similarity was found to be template 2ib5.1.A, which is also a chromoprotein. The secondary structure of this protein was used to construct a 3D model for cjBlue. The predicted 3D structure was a homo octamer. Each monomer subunit had a β barrel with a central α helix.

The 3D structure

To determine if the predicted model was authentic, we generated the Ramachandran Plot for this model by using the SWISS MODEL Workspace. A score of 94% in the most favoured regions as was seen in the Ramachandran plot showed that the predicted model of cjBlue, green chromoprotein is a very good prediction.

To find further information on this protein we used ExPASy - ProtParam tool to compute the various physical and chemical parameters for cjBlue. The computed parameters included the molecular weight, theoretical pI, amino acid composition, atomic composition, extinction coefficient, estimated half-life, instability index, aliphatic index and grand average of hydropathicity (GRAVY).

And finally, it would be a shame if you created a wonderful construct with this part, but then this protein was cleaved by an enzyme produced by your chassis organism, now wouldn't it? To tackle this problem we created a database of all the enzymes that would cleave this chromoprotein, the number and position of the cleavage sites using ExPASy Peptide Cutter.

Cartoon representation of cjBlue.

Physical and chemical properties

Number of amino acids : 232
Molecular weight : 26173.80
Theoretical pI : 7.53
Total number of negatively charged residues (Asp + Glu) : 24
Total number of positively charged residues (Arg + Lys) : 25

Atomic composition:

  •    Carbon (C) - 1151
  •    Hydrogen (H) - 1776
  •    Nitrogen (N) - 314
  •    Oxygen (O) - 347
  •    Sulfur (S) - 19

Formula: C1151H1776N314O347S19
Total number of atoms: 3607

Extinction coefficients:

  •    Extinction coefficients are in units of M-1 cm-1, at 280 nm measured in water.
  •    Ext. coefficient : 28015
  •    Abs 0.1% (=1 g/l): 1.070, assuming all pairs of Cys residues form cystines
  •    Ext. coefficient : 27390
  •    Abs 0.1% (=1 g/l): 1.046, assuming all Cys residues are reduced

Estimated half-life:

  •    The N-terminal of the sequence considered is M (Met).
  •    The estimated half-life is: 30 hours (mammalian reticulocytes, in vitro).
                                                  >20 hours (yeast, in vivo).
                                                  >10 hours (Escherichia coli, in vivo).

Instability index:

  •    The instability index (II) is computed to be 29.86.
  •    The instability index (II) is computed to be 29.86.
  •    This classifies the protein as stable.
  •    Aliphatic index: 58.84
  •    Grand average of hydropathicity (GRAVY): -0.558


Interested in knowing about this protein? click here.

Part Enhancement 2 : RNA thermometer (ROSE)


We used SimRNAweb which is a web server for RNA 3D structure modeling to create a model for the RNA thermometer.

The 3D structure


Interested in seeing the secondary structure of this model? Click here.

Part Enhancement 3 : tsPurple chromoprotein


Similar insilico analysis to cjBlue was done for this part. The sequence for this part was obtained from the iGEM registry and submitted to SWISS MODEL . The protein with the highest sequence similarity was found to be FAR-RED FLUORESCENT PROTEIN AQ143. The secondary structure of this protein was used to construct a 3D model for tsPurple.

The predicted 3D structure was a homotetramer. Each monomer subunit had a β barrel with a central α helix. To determine if the predicted model was authentic, we generated the Ramachandran Plot for this model by using the SWISS MODEL Workspace. A score of 93.3% in the most favoured regions as was seen in the Ramachandran plot showed that the predicted model of tsPurple chromoprotein is a very good prediction.

The 3D structure

Cartoon representation of tsPurple.

Physical and chemical properties

Number of amino acids : 228
Molecular weight : 25546.26
Theoretical pI : 6.65
Total number of negatively charged residues (Asp + Glu) : 27
Total number of positively charged residues (Arg + Lys) : 26

Atomic composition:

  •    Carbon (C) - 1134
  •    Hydrogen (H) - 1747
  •    Nitrogen (N) - 303
  •    Oxygen (O) - 334
  •    Sulfur (S) - 18

Formula: C1134H1747N303O334S18
Total number of atoms: 3536

Extinction coefficients:

  •    Extinction coefficients are in units of M-1 cm-1, at 280 nm measured in water.
  •    Ext. coefficient : 24910
  •    Abs 0.1% (=1 g/l): 0.975, assuming all pairs of Cys residues form cystines
  •    Ext. coefficient : 24410
  •    Abs 0.1% (=1 g/l): 0.956, assuming all Cys residues are reduced

Estimated half-life:

  •    The N-terminal of the sequence considered is M (Met).
  •    The estimated half-life is: 30 hours (mammalian reticulocytes, in vitro).
                                                  >20 hours (yeast, in vivo).
                                                  >10 hours (Escherichia coli, in vivo).

Instability index:

  •    The instability index (II) is computed to be 31.19.
  •    This classifies the protein as stable.
  •    Aliphatic index: 61.97
  •    Grand average of hydropathicity (GRAVY): -0.395
  •    Grand average of hydropathicity (GRAVY): -0.558

Interested in knowing about this protein? click here.

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Lactoshield - SVCE_CHENNAI

Sponsors


igemsvce@gmail.com

Sri Venkateswara College of Engineering
Tamil Nadu, India

    

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