Identification of New Proteins in Follicular Fluid from Mature Human Follicles by Direct Sample Rehydration Method of Two-Dimensional Polyacrylamide Gel Electrophoresis.
10.3346/jkms.2005.20.3.456
- Author:
Han Chul LEE
1
;
Sang Wha LEE
;
Kyo Won LEE
;
Sook Whan LEE
;
Kwang Yul CHA
;
Kye Hyun KIM
;
Suman LEE
Author Information
1. Functional Genomics Lab, CHA Research Institute, Bundang Campus, College of Medicine, Pochon CHA University, Sungnam, Korea. suman@cha.ac.kr
- Publication Type:Original Article ; Research Support, Non-U.S. Gov't
- Keywords:
Follicular Fluid;
Electrophoresis, Gel, Two-Dimensional;
Granulosa Cells
- MeSH:
Adult;
Electrophoresis, Gel, Two-Dimensional/*methods;
Female;
Follicular Fluid/*chemistry/metabolism;
Gene Expression;
Granulosa Cells/metabolism;
Humans;
Ovarian Follicle/*chemistry/metabolism;
Proteins/*analysis/genetics;
RNA, Messenger/genetics/metabolism;
Research Support, Non-U.S. Gov't;
Reverse Transcriptase Polymerase Chain Reaction;
Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization
- From:Journal of Korean Medical Science
2005;20(3):456-460
- CountryRepublic of Korea
- Language:English
-
Abstract:
Human follicular fluid (HFF) includes various biologically active proteins which can affect follicle growth and oocyte fertilization. Thus far, these proteins from mature follicles in human follicular fluid have been poorly characterized. Here, two-dimensional polyacrylamide gel electrophoresis (2-DE) with matrix-assisted laser desorption/ionization-mass spectrometry (MALDI-MS) was used to identify new proteins in HFF. Mature follicular fluids were obtained from five females after oocyte collection during in vitro fertilization (IVF). We directly rehydrated HFF samples, obtained high-resolution 2-DE maps, and processed them for 2-DE and MALDI-MS. One hundred eighty spots were detected and 10 of these spots were identified. By the 2-DE database, six of them had been reported, as proteins already existing in HFF. Hormone sensitive lipase (HSL), Unnamed protein product 1 (UPP1), Unnamed protein product 2 (UPP2), and apolipoprotein A-IV precursor were newly detected. HSL and apolipoprotein A-IV participate in lipid metabolism. UPP1 has a homology with selenocysteine lyase. We found by RT-PCR that these genes are expressed from human primary granulosa cells. The proteins identified here may emerge as potential candidates for specific functions during folliculogenesis, hormone secretion regulation, or oocyte maturation. Further functional analysis of these proteins is necessitated to determine their biological implications.
