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1 s, including the essential invasion receptor Basigin.
2 tein to either of the two common isoforms of basigin.
3 elial crosstalk mediated at least in part by Basigin.
4 of expression of the major invasion receptor basigin.
5 nd that binds with its erythrocyte receptor, Basigin.
6  acid (SA), complement receptor 1 (CR1), and basigin.
7 g the interaction of PfRH5 with its receptor basigin.
8 t mouse basigin can functionally replace fly basigin.
9 fects and neuron-glia interaction defects of basigin.
10 o determine the identity of the receptor for basigin.
11 A-Ripr complex with the erythrocyte receptor basigin(1,2), which is an essential step for entry into
12   We show that RdCVF acts through binding to Basigin-1 (BSG1), a transmembrane protein expressed spec
13  The specific and limited expression of 5A11/Basigin-2 explicitly within photoreceptor cells implies
14                                         5A11/Basigin-2 expression was limited to the retina, specific
15  to lactate or inhibitors in the presence of Basigin-2, a single transmembrane segment (TM)-containin
16  to lactate or inhibitors in the presence of Basigin-2, a single transmembrane segment (TM)-containin
17 lin gene superfamily and has been named 5A11/Basigin-2.
18 sociates with a novel form of human basigin (basigin-3).
19  in tissue remodeling and angiogenesis makes basigin a potential target for the development of strate
20 ial binding of PfRh5/CyRPA/PfRipr complex to basigin, a step linked to the formation of a pore betwee
21 raction with the erythrocyte surface protein basigin (also known as CD147 and EMMPRIN).
22                      CD147 (alias emmprin or basigin), an integral plasma membrane glycoprotein and a
23 recombinant chimeric antibody (Ab-1) against basigin, an erythrocyte receptor necessary for parasite
24 nding of the PfRH5/PCRCR invasion complex to Basigin, an interaction known to be essential for invasi
25  PvTRAg38 binds to two erythrocyte receptors basigin and band 3 through P2 and P4 regions, respective
26 wo single-pass transmembrane proteins, CD147/Basigin and CD44, both of which serve as chaperones for
27 e architecture, presenting binding sites for basigin and inhibitory antibodies at one tip.
28 l molecule that inhibits the binding between Basigin and MCT4.
29 ting that simultaneous blockade of the PfRH5-Basigin and PfRH5/PfRipr/CyRPA interactions produced an
30 functions as a membrane receptor for soluble basigin and this homophilic interaction is not dependent
31  crystal structures of PfRH5 in complex with basigin and two distinct inhibitory antibodies.
32        All variants bound the PfRH5 receptor basigin and were recognized by a panel of monoclonal ant
33 ely blocked using low concentrations of anti-basigin antibodies; importantly, these effects were obse
34                       These results identify Basigin as a potential negative regulator of integrin in
35 able to find evidence supporting the role of basigin as a putative spike binding receptor.
36                     Here, we have identified basigin as the second erythrocyte receptor for PvTRAg38,
37                            Here we show that Basigin associates with integrin at the focal adhesions
38 ssion of a conserved Ig superfamily protein, Basigin, at the glial membrane of Drosophila where it as
39 , rBSG associates with a novel form of human basigin (basigin-3).
40 ng CRISPR/Cas9, we deleted two host factors, basigin (BSG) and CD44, for which no natural nulls exist
41 n mouse chromosome 10, delimited by the gene basigin (Bsg) and marker D10Mit140.
42 ck Swiss mouse strain, delimited by the gene basigin (Bsg) and the marker D10Mit140.
43 atrix metalloproteinase (MMP)-2, MMP-14, and basigin (BSG) are major enzymes involved in the maintena
44 Reticulocyte-binding protein Homolog 5 (RH5)-Basigin (BSG) interaction in host-species selectivity an
45                                              Basigin (BSG) is a multifunctional glycoprotein that pla
46 hat cellular adhesion molecules integrin and basigin (BSG) promote the growth of tumor spheroids.
47 32, impaired in cargo binding, we identified Basigin (BSG), an immunoglobulin superfamily member, as
48 mate association with the glycoprotein CD147/BASIGIN (BSG).
49 identified as the transmembrane glycoprotein basigin (BSG, CD147); more particularly, its low glycosy
50  the photoreceptors demonstrating that mouse basigin can functionally replace fly basigin.
51 zes the surface marker, CD147, also known as Basigin, can effectively kill various malignant HCC cell
52 tion between CAIV and the two MCT chaperones basigin (CD147) and embigin (GP70).
53                                              Basigin (CD147) ligands cyclophilin A and the SARS-CoV-2
54 asma membrane requires association with 5A11/basigin (CD147).
55 or for the virus was recently proposed to be basigin/CD147.
56          The transmembrane Ig domain protein Basigin/CD147/EMMPRIN is highly expressed in the perineu
57 ibodies or other therapeutics targeting host basigin could be an effective treatment for patients inf
58  assays with monoclonal antibodies targeting basigin coupled with PfRh5 next-generation amplicon sequ
59 ed mutant excludes a functional role for the basigin cytoplasmic domain during invasion.
60 to participate in invasion and interact with basigin, did not impact invasive susceptibility of retic
61 age as well as antibody-mediated blockade of Basigin during GC treatment prevents bone loss.
62 exes with a higher affinity than to isolated basigin ectodomain, making it likely that these are the
63                Antibodies targeting PfRH5 or basigin efficiently block parasite invasion in vitro, ma
64       The immunoglobulin superfamily protein basigin (EMMPRIN/CD147) is a cell surface glycoprotein e
65 quire association with the accessory protein basigin, encoded by Bsg, for maturation and trafficking
66 results demonstrate that rBSG interacts with basigin expressed on the surface of fibroblasts and is s
67 of the SARS-CoV-2 spike do not interact with basigin expressed on the surface of human cells, and by
68                         Localization of 5A11/Basigin expression was evaluated by immunoblot, immunohi
69 rane protein CD147 (also known as EMMPRIN or basigin) forms a specific heterodimeric complex in the m
70                            Finally, removing basigin from the surface of human lung epithelial cells
71 nd the extracellular domains are crucial for basigin function in the visual system while the short in
72           It was concluded that cell surface basigin functions as a membrane receptor for soluble bas
73 t is highly conserved with the mouse EMMPRIN/basigin gene.
74 alternative transcription initiation of BSG (Basigin) gene by differentially influencing RNAPII densi
75 srupted, via zinc finger nucleases, MCT4 and BASIGIN genes in colon adenocarcinoma (LS174T) and gliob
76 ultiple highly expressed proteins, including basigin, Glut1, and CD98hc.
77                                         5A11/Basigin has recently been identified as a critical glyco
78              Our previous work on Drosophila basigin has shown that it is required for normal photore
79     However, the biological function of 5A11/Basigin has yet to be determined.
80 king the essential interaction of PfRH5 with basigin in its physiological context.
81  essential role for the erythrocyte receptor basigin in P. falciparum invasion and demonstrate rescue
82                                 Knockdown of Basigin in perineurial glia using RNAi results in signif
83               In contrast, overexpression of basigin in SH-5YSY cells, which poorly express BSG, rest
84                                      Loss of Basigin in the glia results in an overall compression of
85 used to evaluate the number of forms of 5A11/Basigin in the mouse retina.
86 r transgenic fly basigin or transgenic mouse basigin in the photoreceptors demonstrating that mouse b
87                      The genetic deletion of Basigin in the skeletal lineage as well as antibody-medi
88 the neural retina supporting a role for 5A11/basigin in the targeting of these transporters to the pl
89 hermal-shift-assays confirmed ACF binding to basigin in vitro and in live glioblastoma cells, respect
90                     Ab-1 inhibited the PfRH5-basigin interaction and potently blocked erythrocyte inv
91 following: 1) the ability to block the PfRH5-basigin interaction in vitro is predictive of functional
92 sought to determine if disruption of the MCT-Basigin interaction may be achieved with a small molecul
93                                   Drosophila basigin is a cell-surface glycoprotein of the Ig superfa
94                                              Basigin is an essential host receptor for invasion of Pl
95 he interaction with its erythrocyte receptor basigin is essential for invasion.
96               Here, we show that erythrocyte basigin is exclusively found in one of two macromolecula
97                           We determined that Basigin is expressed in close proximity to integrin at t
98                                              Basigin is involved in many physiological functions duri
99                   Interaction between P2 and basigin is stabilized through multiple amino acid residu
100 the extracellular integrin-binding domain of Basigin is sufficient to rescue peripheral glial compres
101     In summary, our results demonstrate that basigin is very likely the apoD receptor and provide add
102                              Emmprin (CD147; basigin) is a cell surface glycoprotein of the immunoglo
103                              Emmprin (CD147; basigin) is a plasma membrane glycoprotein, enriched on
104 lin superfamily glycoprotein CD147 (emmprin; basigin) is associated with an invasive phenotype in var
105 oproteinase inducer) also known as CD147 and basigin, is a member of the immunoglobulin family that i
106  longer form, a splice variant of mouse 5A11/Basigin, is a member of the immunoglobulin gene superfam
107  have found that the Ok blood group antigen, basigin, is a receptor for PfRh5, a parasite ligand that
108 corresponding to the extracellular domain of basigin, it was demonstrated that the native, nonglycosy
109  potently inhibited by soluble basigin or by basigin knockdown, and invasion could be completely bloc
110 asone-treated patients exhibited low ROS and basigin levels.
111               Furthermore, expression of the basigin ligand PfRh5 was the best predictor of donor par
112                                    The PfRh5-Basigin ligand-receptor interaction is an essential step
113      The EBA-175/glycophorin A (GPA) and Rh5/basigin ligand-receptor interactions, referred to as inv
114 n is not dependent upon glycosylation of the basigin ligand.
115 culocyte-binding protein homolog 5 (RH5) and basigin makes RH5 a prime target for broadly neutralizin
116 disruption of MCT binding to their chaperon, Basigin, may be an effective approach to target GSC and
117 ey do reduce its binding to basigin-PMCA and basigin-MCT complexes.
118 es related to mitochondrial function and the basigin network.
119 family that includes mammalian EMMPRIN/CD147/basigin, neuroplastin, and embigin.
120 itudes in the electroretinograms in the 5A11/basigin null mouse (Bsg(-/-)) may be linked to altered e
121 e invasion was potently inhibited by soluble basigin or by basigin knockdown, and invasion could be c
122 oproteinase inducer (EMMPRIN), also known as basigin or CD147, is a glycoprotein that is enriched on
123 scued by expression of either transgenic fly basigin or transgenic mouse basigin in the photoreceptor
124 15 monoclonal antibodies recognizing EMMPRIN/basigin/OX-47/M6, a 45-55-kDa transmembrane protein with
125 fluenced by endemicity levels, and the PfRh5-basigin pathway is a potential vaccine target.
126 meric basigin, they do reduce its binding to basigin-PMCA and basigin-MCT complexes.
127 ports indicate the presence of multiple 5A11/Basigin polypeptides within the retina.
128                    Using a novel recombinant basigin protein (rBSG) corresponding to the extracellula
129             To determine what regions of the basigin protein are required for each of these functions
130 e that this ancestral protein could bind the basigin receptor from both humans and gorillas.
131 he identity of the cell surface receptor for basigin remains controversial.
132 C, and D (GPA/B/C/D), complement receptor 1, basigin, semaphorin 7a, Band 3/ GPA, Kx, and heparan sul
133 osaic animals that are mutant in the eye for basigin show altered cell structure with nuclei, mitocho
134 rting enzyme 2 was rarely expressed, whereas basigin showed diffuse expression, and alanyl aminopepti
135 ractions as weak or weaker than the proposed basigin-spike binding, we report no evidence for a direc
136 e transport isoform 1 (MCT1) and its partner basigin that are highly enriched on retinal glia and mye
137  an effort to determine the function of 5A11/Basigin, the molecular diversity of its expression was e
138 , when administered to 2-year-old mice, anti-Basigin therapy reinstates bone remodeling to significan
139 er and (2) disrupting a key interaction with basigin, thereby reducing cell-surface localization.
140 not reduce the binding of PfRH5 to monomeric basigin, they do reduce its binding to basigin-PMCA and
141                               The ability of basigin to stimulate expression of molecules involved in
142 s well mechanisms still under consideration (BASIGIN) to infect and spread throughout the CNS.
143                                     Two 5A11/Basigin transcripts of approximately 1.5 kb and approxim
144  performed to determine the sequence of 5A11/Basigin transcripts.
145 h of these functions, we have created mutant basigin transgenes coding for proteins that are altered
146 ermore, Ok(a-) erythrocytes, which express a basigin variant that has a weaker binding affinity for P
147 cificity of interaction between PvTRAg38 and basigin was confirmed by direct interaction where basigi
148 r mediator of SA-independent invasion, while basigin was essential for both SA-dependent and SA-indep
149 in was confirmed by direct interaction where basigin was specifically recognized by P2 and not by the
150      In addition, antibodies against CR1 and basigin were used to determine the contributions of thes
151 N-glycan exposed on the human receptor CD147/Basigin, while fucosylated derivatives of this N-glycan
152  comparision of the crystal structure of Rh5-basigin with the cryo-electron microscopy structure of R

 
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