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Molecular Weight Determination of Unknown Proteins for NASA/JPL PAIR Program August 24, 2001. Barbara Falkowski Falgun Patel Celia Smith. The Overall Goal. To determine molecular weight of unknown electrophoresis data. Method to Achieve the Goal.
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Molecular Weight Determination of Unknown Proteinsfor NASA/JPL PAIR Program August 24, 2001 Barbara Falkowski Falgun Patel Celia Smith
The Overall Goal • To determine molecular weight of unknown electrophoresis data
Method to Achieve the Goal • Measure distances of unknown standards with PhotoShop and Spotviewer • Decide whether Spotviewer or Photoshop is the better measuring tool. • Run models on standard proteins • Decide which model(s) work the best for the standards • Run model(s) on unknown proteins. Decide which model(s) worked the best on the unknowns
SpotViewer Disadvantages • Did not measure dye-front distance • One needed to go into Photoshop to mark or crop the dye-front distance. • Spotviewer missed bands • Did not always pick up bands that were thin, blurry or close together. • Sometimes gave two measurement values to one band • Or gave values that were associated with any band. • Did not pick up very light bands.
PhotoShop Advantages • Did not need assistance from another program. • Not as time consuming • Light bands could be more easily discerned through color inversion/manipulation of the image. • This also worked well with tightly packed, thin and blurred bands.
Quadratic Regression Quadratic Cross Validation SLIC Log-Linear Model Log-Log Model Local Linear Model Quadratic Interpolation Gels/Protein Used Models Tested • Vitelline Envelopes (VE) for two species (Strongylocentrotus purpuratus and Lytechinus pictus) • Vitelline Envelopes for two methods (DTT and mechanically isolated)
Which model worked the best? • No single model was best for all of the gels. • It was found that different models worked better for different gels. Quadratic Regression Model - 15 % Gel #1 S.purp/L.pictus VE DTT Removal SLIC Model - Gradient Gel #2 Jelly + Seminal Plasma + VE Time Courses LOG-LOG Model - 12. 5% Gels Gel #4 VE + Tris Supernatant Time Course and Gel # 6 VE + Tris Pellet Time Course
Took Quadratic Regression of standards to find the intercept and coefficients. • Used the intercept and coefficients in the equation: • LOG MW = RM^2*a +RM*b +c • Put the relative mobility of the unknowns into the equation to come up with the following results:
What type of Cross Validation was done? • Quadratic Cross Validation using relative mobility and Log Molecular Weight • Cross Validation was not chosen at all • The predicted value for the missing band was not close the the actual value in any of the gel cases.
Why was the SLIC Model chosen for the Gradient Gel #2 ? • Residual Sum = 0.00 • Residual Squared Sum = 0.00 • Largest R^2 = 0.99
Compare Values: • SLIC Type Models: Log( LN(MW) ) = A + B * LN( -LN(RM) ) • Compare Log Molecular Weight X = e ^ ( LN( X ) ) • Convert Log( LN(MW) ) into Log( MW ) Log( MW) = Log( e ^ LN(MW) )
Why was the LOG-LOG Model Chosen for 12.5% Gels • LOG-LOG Model worked best for the 12.5% Gels (Gel #4 VE + Tris Supernatant Time Course and Gel # 6 VE + Tris Pellet Time Course) • Small residuals • R^2 > .9 • Residuals did not have large sections of positive or negative.
The Log-Log Model • The Log-Log model is of the form: Log(MW)=a+bLog(RM)+cLog(RM)^2 • It incorporates the Log model and the quadratic model to make a more successful madel.
Conclusion Different models worked better on different on certain gel types. The Quadratic Regression Model on the 15% gel, SLIC Model for the gradient gel and the LOG-LOG Model worked best for 12.% gels. This process could be much improved if there was more data on the different gel types.
Thank You Open for Questions…