Subcellular localization of GTPase of immunity-associated protein 2.
- Author:
Hong Quan QIN
1
;
You ZHENG
2
;
Man Na WANG
2
;
Zheng Rong ZHANG
2
;
Zu Biao NIU
2
;
Li MA
1
;
Qiang SUN
2
;
Hong Yan HUANG
3
;
Xiao Ning WANG
1
Author Information
1. School of Laboratory Medicine and Biotechnology, Institute of Molecular Immunology, Southern Medical University, Guangzhou 510515, China.
2. Institute of Biotechnology, Academy of Military Medical Sciences, Beijing100071, China.
3. Department of Glioma, Beijing Shijitan Hospital, Capital Medical University, Beijing100038, China.
- Publication Type:Journal Article
- MeSH:
Amino Acid Sequence;
Cytoplasm;
GTP Phosphohydrolases;
Humans;
Membrane Proteins;
Nuclear Export Signals;
Nuclear Localization Signals;
Recombinant Fusion Proteins;
Transfection
- From:
Journal of Peking University(Health Sciences)
2020;52(2):221-226
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVE:To analyze the subcellular localization of GTPase of immunity-associated protein 2 (GIMAP2) for the further functional study.
METHODS:In the study, we first obtained the protein sequences of GTPase of immunity-associated protein 2 (GIMAP2) from National Center for Biotechnology Information (NCBI) database, and then performed a prediction analysis of its transmembrane structure, nuclear localization signal (NLS), nuclear export signal (NES) and subcellular localization through bioinformatics online tools. GIMAP2 gene amplified by PCR was inserted into the expression vector pQCXIP-mCherry-N1 and positive clones were selected by ampicillin resistance. After using methods to extract and purify, the sequenced recombinant plasmid pQCXIP-GIMAP2-mCherry, together with the retroviral packaging plasmids VSVG and Gag/pol, was transferred into HEK293FT cells by liposomes for virus packaging. The virus supernatant was collected 48 h after transfection and directly infected the human breast cancer cell line MDA-MB-436. Immunofluorescence staining was constructed to detect the localization of endogenous and exogenous GIMAP2 in MDA-MB-436 cells. Meanwhile, green fluorescent chemical dyes were used to label mitochondria, endoplasmic reticulum, and lipid droplets in living MDA-MB-436 cells stably expressing the GIMAP2-mCherry fusion protein. Images for the three dye-labeled organelles and GIMAP2-mCherry fusion protein were captured by super-resolution microscope N-SIM.
RESULTS:Bioinformatics analysis data showed that GIMAP2 protein composed of 337 amino acids might contain two transmembrane helix (TM) structures at the carboxyl terminus, of which TMs were estimated to contain 40-41 expected amino acids, followed by the residual protein structures toward the cytoplasmic side. NES was located at the 279-281 amino acids of the carboxyl terminus whereas NLS was not found. GIMAP2 might locate in the lumen of the endoplasmic reticulum. Sequencing results indicated that the expression vector pQCXIP-GIMAP2-mCherry was successfully constructed. Fluorescent staining confirmed that GIMAP2-mCherry fusion protein, co-localized well with endogenous GIMAP2, expressed successfully in the endoplasmic reticulum and on the surface of lipid droplets in MDA-MB-436 cells.
CONCLUSION:GIMAP2 localizes in the endoplasmic reticulum and on the surface of LDs, suggesting potential involvement of GIMAP2 in lipid metabolism.
