November 1997
Volume 38, Issue 12
Free
Articles  |   November 1997
Complete map and identification of the phosphorylation site of bovine lens major intrinsic protein.
Author Affiliations
  • K L Schey
    Department of Pharmacology, Medical University of South Carolina, Charleston 29425, USA.
  • J G Fowler
    Department of Pharmacology, Medical University of South Carolina, Charleston 29425, USA.
  • J C Schwartz
    Department of Pharmacology, Medical University of South Carolina, Charleston 29425, USA.
  • M Busman
    Department of Pharmacology, Medical University of South Carolina, Charleston 29425, USA.
  • J Dillon
    Department of Pharmacology, Medical University of South Carolina, Charleston 29425, USA.
  • R K Crouch
    Department of Pharmacology, Medical University of South Carolina, Charleston 29425, USA.
Investigative Ophthalmology & Visual Science November 1997, Vol.38, 2508-2515. doi:
  • Views
  • PDF
  • Share
  • Tools
    • Alerts
      ×
      This feature is available to authenticated users only.
      Sign In or Create an Account ×
    • Get Citation

      K L Schey, J G Fowler, J C Schwartz, M Busman, J Dillon, R K Crouch; Complete map and identification of the phosphorylation site of bovine lens major intrinsic protein.. Invest. Ophthalmol. Vis. Sci. 1997;38(12):2508-2515.

      Download citation file:


      © ARVO (1962-2015); The Authors (2016-present)

      ×
  • Supplements
Abstract

PURPOSE: To determine the complete primary structure, including posttranslational modifications, of bovine lens major intrinsic protein (MIP) using a recently developed combination of liquid chromatography and mass spectrometry. METHODS: The MIP was isolated from bovine lenses by sucrose gradient centrifugation and was cleaved with cyanogen bromide (CNBr). A high-performance liquid chromatographic system, developed for hydrophobic protein analysis, was used to separate the cleavage fragments. Matrix-assisted laser desorption ionization and electrospray tandem mass spectrometry were employed to obtain molecular weight and sequence data from bovine MIP CNBr fragments, directly or after subsequent digestion with trypsin. RESULTS: The complete sequence of bovine MIP was mapped by molecular weight measurements of CNBr fragments, confirming the reported DNA sequence. The C-terminal peptide (177 to 263) was fully sequenced and the major site of phosphorylation was determined to be at serine 235 rather than at the previously reported serine 243. The level of phosphorylation in the native protein was determined to be 25%. No other posttranslational derivatizations were observed with the exception of the previously detected deamidation of asparagine 246. CONCLUSIONS: These results represent the first complete MIP sequence map at the amino acid level and identify the single major phosphorylation site at serine 235.

×
×

This PDF is available to Subscribers Only

Sign in or purchase a subscription to access this content. ×

You must be signed into an individual account to use this feature.

×