EFFECT OF STORAGE ON PROTEIN-CONCENTRATION OF TEAR SAMPLES

Citation
T. Sitaramamma et al., EFFECT OF STORAGE ON PROTEIN-CONCENTRATION OF TEAR SAMPLES, Current eye research (Print), 17(10), 1998, pp. 1027-1035
Citations number
36
Categorie Soggetti
Ophthalmology
ISSN journal
02713683
Volume
17
Issue
10
Year of publication
1998
Pages
1027 - 1035
Database
ISI
SICI code
0271-3683(1998)17:10<1027:EOSOPO>2.0.ZU;2-4
Abstract
Purpose. To determine the effect of storage on protein concentration o f tear samples stored at room temperature (RT), 4 degrees C, -20 degre es C and -70 degrees C. Methods. Total protein concentration of closed , open (basal tears) and reflex tears (stimulated tears) was measured by modified Bradford's method. SDS-PAGE gel electrophoresis was used t o determine the intensity of protein bands. Quantity of various tear p roteins was determined by HPLC analysis. Results. Compared to control samples (0 h) protein concentrations decreased significantly in tear s amples stored beyond 4 h (for closed) and 8 h (for open and reflex) at RT. However, no significant change in protein concentrations was obse rved in closed and reflex tears when stored up to 1 week at 4 degrees C, up to 2 months at -20 degrees C; and up to 4 months at -70 degrees C. Multiple freeze-thaw procedures (6 x per day at 2 h intervals) resu lted in 8% decrease (at -20 degrees C) and 10% decrease (at -70 degree s C) of protein concentrations in closed eye tears. SDS-PAGE analysis of tear samples stored at -20 degrees C and -70 degrees C for 4 months greatly affected the intensity of the protein bands. HPLC analysis of tear samples stored at these conditions showed the significant reduct ion in the peak corresponding to secretory IgA in closed eye tears and a split in the peak corresponding to lysozyme in case of reflex tears . Conclusions. Reduction in the total protein concentration, intensity of the protein bands as well as changes in the quantity of tear prote ins were observed in the tear samples stored for longer duration of ti me at various temperatures.