TY - JOUR
T1 - Proteomic analysis of human vitreous humor
AU - Murthy, Krishna R.
AU - Goel, Renu
AU - Subbannayya, Yashwanth
AU - Jacob, Harrys K.C.
AU - Murthy, Praveen R.
AU - Manda, Srikanth Srinivas
AU - Patil, Arun H.
AU - Sharma, Rakesh
AU - Sahasrabuddhe, Nandini A.
AU - Parashar, Arun
AU - Nair, Bipin G.
AU - Krishna, Venkatarangaiah
AU - Prasad, T. S.Keshava
AU - Gowda, Harsha
AU - Pandey, Akhilesh
N1 - Funding Information:
We thank the Department of Biotechnology (DBT) of the Government of India for research support to the Institute of Bioinformatics, Bangalore. Nandini A. Sahasrabuddhe and Harrys K.C. Jacob are recipients of Senior Research Fellowship from the Council for Scientific and Industrial Research (CSIR), India. Srikanth Srinivas Manda is a recipient of Senior Research Fellowship from University Grants Commission (UGC), India. Rakesh Sharma is a Research Associate supported by DBT. Harsha Gowda is a Wellcome Trust/DBT India Alliance Early Career Fellow. Dr. T. S. Keshava Prasad is the recipient of a research grant on “Development of Infrastructure and a Computational Framework for Analysis of Proteomic Data” from DBT.
Publisher Copyright:
© 2014 Murthy et al.; licensee BioMed Central Ltd.
PY - 2014/7/14
Y1 - 2014/7/14
N2 - Background: The vitreous humor is a transparent, gelatinous mass whose main constituent is water. It plays an important role in providing metabolic nutrient requirements of the lens, coordinating eye growth and providing support to the retina. It is in close proximity to the retina and reflects many of the changes occurring in this tissue. The biochemical changes occurring in the vitreous could provide a better understanding about the pathophysiological processes that occur in vitreoretinopathy. In this study, we investigated the proteome of normal human vitreous humor using high resolution Fourier transform mass spectrometry. Results: The vitreous humor was subjected to multiple fractionation techniques followed by LC-MS/MS analysis. We identified 1,205 proteins, 682 of which have not been described previously in the vitreous humor. Most proteins were localized to the extracellular space (24%), cytoplasm (20%) or plasma membrane (14%). Classification based on molecular function showed that 27% had catalytic activity, 10% structural activity, 10% binding activity, 4% cell and 4% transporter activity. Categorization for biological processes showed 28% participate in metabolism, 20% in cell communication and 13% in cell growth. The data have been deposited to the ProteomeXchange with identifier PXD000957. Conclusion: This large catalog of vitreous proteins should facilitate biomedical research into pathological conditions of the eye including diabetic retinopathy, retinal detachment and cataract.
AB - Background: The vitreous humor is a transparent, gelatinous mass whose main constituent is water. It plays an important role in providing metabolic nutrient requirements of the lens, coordinating eye growth and providing support to the retina. It is in close proximity to the retina and reflects many of the changes occurring in this tissue. The biochemical changes occurring in the vitreous could provide a better understanding about the pathophysiological processes that occur in vitreoretinopathy. In this study, we investigated the proteome of normal human vitreous humor using high resolution Fourier transform mass spectrometry. Results: The vitreous humor was subjected to multiple fractionation techniques followed by LC-MS/MS analysis. We identified 1,205 proteins, 682 of which have not been described previously in the vitreous humor. Most proteins were localized to the extracellular space (24%), cytoplasm (20%) or plasma membrane (14%). Classification based on molecular function showed that 27% had catalytic activity, 10% structural activity, 10% binding activity, 4% cell and 4% transporter activity. Categorization for biological processes showed 28% participate in metabolism, 20% in cell communication and 13% in cell growth. The data have been deposited to the ProteomeXchange with identifier PXD000957. Conclusion: This large catalog of vitreous proteins should facilitate biomedical research into pathological conditions of the eye including diabetic retinopathy, retinal detachment and cataract.
KW - Body fluid proteomics
KW - OFFGEL electrophoresis
KW - Protein biomarkers
KW - Proteome discoverer
KW - Retina
KW - SCX chromatography
KW - Secreted proteins
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U2 - 10.1186/1559-0275-11-29
DO - 10.1186/1559-0275-11-29
M3 - Article
AN - SCOPUS:84922793574
SN - 1542-6416
VL - 11
JO - Clinical Proteomics
JF - Clinical Proteomics
IS - 1
M1 - 29
ER -