Solute carrier family 2, facilitated glucose transporter member 5 (SLC2A5), also known as fructose transporter or glucose transporter type 5, small intestine (GLUT-5), is a protein in humans that is encoded by the SLC2A5 gene. It is a fructose transporter mainly expressed on the apical border of enterocytes in the small intestine.
Basic Information of SLC2A5 | |
Protein Name | Solute carrier family 2, facilitated glucose transporter member 5 |
Gene Name | SLC2A5 |
Aliases | Fructose transporter, Glucose transporter type 5, small intestine, GLUT-5 |
Organism | Homo sapiens (Human) |
UniProt ID | P22732 |
Transmembrane Times | 12 |
Length (aa) | 496 |
Sequence | MAGVVHVSLAALLLLPMAPAMHSDCIFKKEQAMCLEKIQRANELMGFNDSSPGCPGMWDNITCWKPAHVGEMVLVSCPELFRIFNPDQVWETETIGESDFGDSNSLDLSDMGVVSRNCTEDGWSEPFPHYFDACGFDEYESETGDQDYYYLSVKALYTVGYSTSLVTLTTAMVILCRFRKLHCTRNFIHMNLFVSFMLRAISVFIKDWILYAEQDSNHCFISTVECKAVMVFFHYCVVSNYFWLFIEGLYLFTLLVETFFPERRYFYWYTIIGWGTPTVCVTVWATLRLYFDDTGCWDMNDSTALWWVIKGPVVGSIMVNFVLFIGIIVILVQKLQSPDMGGNESSIYFSCVQKCYCKPQRAQQHSCKMSELSTITLRLARSTLLLIPLFGIHYTVFAFSPENVSKRERLVFELGLGSFQGFVVAVLYCFLNGEVQAEIKRKWRSWKVNRYFAVDFKHRHPSLASSGVNGGTQLSILSKSSSQIRMSGLPADNLAT |
GLUT5 (SLC2A5) is a fructose transporter encoded by the SLC2A5 gene of the SLC2 family. It is primarily expressed in the jejunal region of the small intestine. Lower levels of the protein are found in kidney, brain, skeletal muscle, and adipose tissue. Studies have shown that it could mediate fructose absorption in the jejunum at the apical, potentially also basolateral membrane, of the epithelial cells into the portal vein. During the past years, the expression level of SLC2A5 is associated with numerous diseases. For example, the expression of SLC2A5 is elevated in breast cancer cell lines MCF7 and MDA-MB-231 and associated with higher fructose uptake rate. Recently, it has shown that the expression of SLC2A5 in tumor cells of patients with AML is increased and is negatively correlated with the prognosis of patients. Furthermore, SLC2A5 is significantly upregulated in lung adenocarcinoma patients and overexpression of SLC2A5 is highly correlated with poor patient survival.
Fig.1 Fructose promotes lung adenocarcinoma cell survival and metastasis through SLC2A5. (Weng, 2018)
This article suggests that SLC2A5 is significantly upregulated in lung adenocarcinoma (LUAD) patients and overexpression of SLC2A5 is highly correlated with poor prognosis of LUAD patients. It indicates that GLUT5 may be used as a potential target alone or in combination with other treatment for lung cancer therapy.
This article suggests that PPF MM represents a promising nanoscale carrier system to achieve GLUT5-mediated cell-specific delivery in cancer therapy.
This article aims to explore the possible roles of glucose transport 5 (Glut5) in imatinib resistance in the Ph+ acute lymphoblastic leukemia cell (Ph+ ALL). It finds that high expression of SLC2A5 and Glut5 protein in SUP-B15/R cells could lead to increased fructose absorption, and further activates the PI3K/AKT pathway which causes the SUP-B15 cell resistance to imatinib.
This article aims to determine the distribution of glucose transporter 5 (GLUT5), which preferentially transports fructose, in the rat brain by immunohistochemistry and western blotting. It suggests that GLUT5 may transport fructose in subsets of the glia and neurons for an energy source of these cells.
This article suggests that fructose and GluT5 play an important role in regulating adipose differentiation.
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