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Posters
January 2004

 

Stabilization of Lysozyme Mass Extracted from SH Contact Lens Materials

L N Subbaraman (1A) , M Senchyna (1B), L Jones (1B)
(A) School of Optometry, (B) Centre for Contact Lens Research, (1) University of Waterloo, Waterloo, ON, Canada.

 

Purpose: Preliminary results in our laboratory demonstrated that lysozyme deposits extracted from silicone-hydrogel (SH) contact lens materials demonstrated a loss in total mass as a function of storage time when assessed by Western blotting (WB). This loss represents a potential source of error when quantifying total lysozyme deposition. Thus, the purpose of this work was to devise a method whereby lysozyme mass would be preserved over time and would be compatible with our previously described WB procedure (1).

Methods: Lysozyme deposits from human worn lenses were extracted using a 50:50 mixture of 0.2% trifluoroacetic acid and acetonitrile. Extracts were lyophilized to dryness, then resuspended in either Reconstitution Buffer (RB) (10mM Tris-HCl, 1mM EDTA) or Modified Reconstitution Buffer (MRB) (RB + 0.9% saline). BioStab (1 in 4 parts) (Sigma) was added to one half of the samples from each buffer group. 1 mL of each of the samples was immediately subjected to SDS PAGE and WB on a PhastSystem (Pharmacia), while the remaining volume was aliquoted and stored at -20 °C or -70 °C and subjected to the same procedures after 48 hours of storage. All WBs were imaged and quantified on a Storm 840 Imaging system. Comparison of lysozyme band intensity in stored versus fresh samples enabled calculation of percentage mass loss of lysozyme.

Results:
As can be seen in Table 1,resuspension of lyophilized SH lens extracts in MRB and BioStab provided essentially 100% protection to lysozyme mass when stored in frozen aliquots.

Conclusion: We have optimized a procedure using MRB, BioStab and storage at -70 oC, whereby the extracted mass of lysozyme deposits found on SH lenses can be preserved without loss to facilitate accurate quantitation via our WB procedure .

Table 1: Percentage mass loss of Lysozyme after 48 hours of storage:

 

-20 ° C

P

-70 ° C

P

No Biostab

With Biostab

No Biostab

With Biostab

RB

33.2% ± 0.5

15.8% ±0.5

<0.001

31.3% ±1.5

14.1% ±0.9

<0.001

MRB

19.2% ± 4.5

0.9% ± 0.8

<0.001

17.1% ± 2.8

0.6% ± 0.8

<0.001

P

<0.001

<0.001

 

<0.001

<0.001

 

1. Senchyna M, Jones L, Louie D, May C, Forbes I, Glasier M: Quantitative and conformational characterization of lysozyme deposited on balafilcon and etafilcon contact lens materials. Curr Eye Res 2004; 28: 25-36.

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