Method of identifying intracellular secretory protein or tissue-specific secretory protein
The present invention relates to a method of identifying an intracellular secretory protein or tissue-specific secretory protein, by using a proximity labeling system. When the method according to the present invention is used, it is possible to clearly identify an intracellular secretory protein and to dynamically track the spatiotemporal dynamics of a secretory protein secreted from a specific tissue in a living subject such that it can be effectively utilized for the research on endocrine signals between tissues, and particularly, since it can be applied in situ, the scope of application can be further expanded. Therefore, the present invention can be applied to various disease models or tissues to discover new biomarkers and therapeutic target proteins associated with diseases.
1 . A method for identifying an intracellular secretory protein or tissue-specific secretory protein, comprising the steps of:
(a) expressing a fusion protein in cells or expressing the fusion protein tissue-specifically in a subject, wherein the fusion protein is a fusion protein in which an ER lumen targeting membrane protein and a biotin ligase are fused, wherein the biotin ligase comprises at least one selected from the group consisting of BioID and TurboID;
(b) obtaining a biotinylated protein or peptide from a sample of the cells or the subject; and
(c) analyzing the protein or peptide to identify a secretory protein or peptide.
2 . The method of claim 1 , wherein step (a) treats biotin after expressing the fusion protein in cells or expressing the fusion protein tissue-specifically in a subject.
3 . The method of claim 1 , wherein the ER lumen targeting membrane protein has ER transmembrane domain.
4 . The method of claim 1 , wherein the biotin ligase is fused to the N-terminus or C-terminus of the ER lumen targeting membrane protein or inserted into the ER lumen targeting membrane protein.
5 . The method of claim 1 , wherein the fusion protein labels a secretory protein or peptide in the process of the secretory protein or peptide passing through the endoplasmic reticulum membrane.
6 . The method of claim 1 , wherein the cells are selected from the group consisting of cancer cells, kidney cells, skin cells, ovarian cells, synovial cells, peripheral blood mononuclear cells, fibroblasts, fibrous cells, nerve cells, epithelial cells, keratinocytes, hematopoietic cells, melanocytes, chondrocytes, macrophages, muscle cells, blood cells, bone marrow cells, lymphocyte cells, mononuclear cells, lung cells, pancreatic cells, liver cells, gastric cells, intestinal cells, cardiac cells, brain cells, bladder cells, urethral cells, embryonic germ cells, cumulus cells and a combination thereof.
7 . The method of claim 1 , wherein step (a) either
(i) delivers a recombinant virus expressing the fusion protein to a subject tissue-specifically, or
(ii) expresses the fusion protein by using a transgenic mouse expressing the fusion protein tissue-specifically by Cre-LoxP.
8 . The method of claim 7 , wherein the recombinant virus is any one selected from the group consisting of adenovirus, retrovirus, herpesvirus, lentivirus, herpesvirus and reovirus.
9 . The method of claim 1 , wherein the tissue is any one selected from the group consisting of brain, lung, liver, stomach, intestine, heart, kidney, skin, ovary, testis, nerve, muscle, bone marrow, bone, adrenal gland, pituitary, prostate, spleen, thyroid, uterus, adipose, artery, vein, pancreas and bladder.
10 . The method of claim 1 , wherein the biotinylated protein or peptide is obtained by adding Streptavidin beads, Neutravidin beads or anti-biotin beads.
11 . The method of claim 1 , wherein the sample is any one selected from the group consisting of cells, blood, urine and body fluid.
12 . The method of claim 1 , wherein the analysis is performed by using at least one method selected from the group consisting of mass spectrometry, western blot, fluorescence microscopy, dot blot and ELISA.