A Chick Retinal Proteome Database and Differential Retinal Protein Expressions during Early Ocular Development

Thomas C. Lam, King-Kit Li, Samuel C. L. Lo,* Jeremy A. Guggenheim,§ and Chi Ho To*
Laboratory of Experimental Optometry, Centre for Myopia Research, School of Optometry, The Hong Kong Polytechnic University, Hung Hom, Kowloon, Hong Kong SAR, China, The Proteomic Task Force, Department of Applied Biology and Chemical Technology, The Hong Kong Polytechnic University, Kowloon, Hong Kong SAR, China, The State Key Laboratory of Chinese Medicine and Molecular Pharmacology, Shenzhen, China, and Department of Optometry & Vision Sciences, Cardiff University, Redwood Building, King Edward VII Avenue, Cardiff, United Kingdom
J. Proteome Res., 2006, 5 (4), pp 771–784
DOI: 10.1021/pr050280n
Publication Date (Web): February 22, 2006
Copyright © 2006 American Chemical Society

 School of Optometry, The Hong Kong Polytechnic University.

,
*

 Authors for correspondence. Prof. Chi-Ho To, School of Optometry, The Hong Kong Polytechnic University, Hung Hom, Kowloon, Hong Kong SAR, China; e-mail, sochto@inet.polyu.edu.hk; tel, (852) 2766 6102; fax, (852) 2764 6051. Prof. Samuel Chun-Lap Lo, Department of Applied Biology and Chemical Technology, The Hong Kong Polytechnic University, Hung Hom, Kowloon, Hong Kong SAR, China; e-mail, bcsamlo@inet.polyu.edu.hk; tel, (852) 34008669; fax, (852) 2364 9932.

,

 Department of Applied Biology and Chemical Technology, The Hong Kong Polytechnic University, and The State Key Laboratory of Chinese Medicine and Molecular Pharmacology.

,

 Both author contributed equally.

,
§

 Cardiff University.

Abstract

Abstract Image

Proteomics approach as a research tool has gained popularity in a growing number of basic and clinical researches. However, proteomic research has yet to gain significant momentum in eye research. Hence, we decided to build a retinal proteome database using postnatal retinal tissue from chick, a commonly used animal model in eye research. Employing 2-D gels with the coverage of 3−10 pH gradients, we were able to resolve hundreds of proteins from young chick retinae. Among them, 155 high abundant proteins were identified by Peptide Mass Fingerprinting (PMF) after the Matrix-Assisted Laser Desorption Ionization-Time-of-Flight Mass Spectrometry (MALDI-TOF MS). These proteins were then classified according to their functions. Making use of the retinal database, we were able to identify several differentially expressed proteins that might be involved in early retinal development by comparing the 2-DE maps of chick retinal tissues (3, 10, and 20 days after hatching). With the current proteomics approach, we not only documented the most abundant soluble proteins in the chick retinal tissue, but also demonstrated the dynamic protein expression changes during early ocular development. This represents one of the first steps in building a complete protein database in chick retinae which is applicable to the study of eye diseases from a few selected protein candidates to the whole proteome. Proteomic technology may provide a high throughput platform for advancing eye research in the feasible future.

Keywords: two-dimensional gel electrophoresis • chick • development • proteomics • proteome • retina • mass spectrometry

Tools

History

  • Published In Issue April 07, 2006
  • Received August 24, 2005

Recommend & Share

Related Content

Other ACS content by these authors: