A simple detection method for low-affinity membrane protein interactions by baculoviral display.

BACKGROUND: Membrane protein interactions play an important role in cell-to-cell recognition in various biological activities such as in the immune or neural system. Nevertheless, there has remained the major obstacle of expression of the membrane proteins in their active form. Recently, we and othe...

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Main Authors: Toshiko Sakihama, Takato Sato, Hiroko Iwanari, Toshio Kitamura, Shimon Sakaguchi, Tatsuhiko Kodama, Takao Hamakubo
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2008-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC2602974?pdf=render
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spelling doaj-0060a15c5e014846bc9f485a543701272020-11-25T01:58:23ZengPublic Library of Science (PLoS)PLoS ONE1932-62032008-01-01312e402410.1371/journal.pone.0004024A simple detection method for low-affinity membrane protein interactions by baculoviral display.Toshiko SakihamaTakato SatoHiroko IwanariToshio KitamuraShimon SakaguchiTatsuhiko KodamaTakao HamakuboBACKGROUND: Membrane protein interactions play an important role in cell-to-cell recognition in various biological activities such as in the immune or neural system. Nevertheless, there has remained the major obstacle of expression of the membrane proteins in their active form. Recently, we and other investigators found that functional membrane proteins express on baculovirus particles (budded virus, BV). In this study, we applied this BV display system to detect interaction between membrane proteins important for cell-to-cell interaction in immune system. METHODOLOGY/PRINCIPAL FINDINGS: We infected Sf9 cells with recombinant baculovirus encoding the T cell membrane protein CD2 or its ligand CD58 and recovered the BV. We detected specific interaction between CD2-displaying BV and CD58-displaying BV by an enzyme-linked immunosorbent assay (ELISA). Using this system, we also detected specific interaction between two other membrane receptor-ligand pairs, CD40-CD40 ligand (CD40L), and glucocorticoid-induced TNFR family-related protein (GITR)-GITR ligand (GITRL). Furthermore, we observed specific binding of BV displaying CD58, CD40L, or GITRL to cells naturally expressing their respective receptors by flowcytometric analysis using anti-baculoviral gp64 antibody. Finally we isolated CD2 cDNA from a cDNA expression library by magnetic separation using CD58-displaying BV and anti-gp64 antibody. CONCLUSIONS: We found the BV display system worked effectively in the detection of the interaction of membrane proteins. Since various membrane proteins and their oligomeric complexes can be displayed on BV in the native form, this BV display system should prove highly useful in the search for natural ligands or to develop screening systems for therapeutic antibodies and/or compounds.http://europepmc.org/articles/PMC2602974?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Toshiko Sakihama
Takato Sato
Hiroko Iwanari
Toshio Kitamura
Shimon Sakaguchi
Tatsuhiko Kodama
Takao Hamakubo
spellingShingle Toshiko Sakihama
Takato Sato
Hiroko Iwanari
Toshio Kitamura
Shimon Sakaguchi
Tatsuhiko Kodama
Takao Hamakubo
A simple detection method for low-affinity membrane protein interactions by baculoviral display.
PLoS ONE
author_facet Toshiko Sakihama
Takato Sato
Hiroko Iwanari
Toshio Kitamura
Shimon Sakaguchi
Tatsuhiko Kodama
Takao Hamakubo
author_sort Toshiko Sakihama
title A simple detection method for low-affinity membrane protein interactions by baculoviral display.
title_short A simple detection method for low-affinity membrane protein interactions by baculoviral display.
title_full A simple detection method for low-affinity membrane protein interactions by baculoviral display.
title_fullStr A simple detection method for low-affinity membrane protein interactions by baculoviral display.
title_full_unstemmed A simple detection method for low-affinity membrane protein interactions by baculoviral display.
title_sort simple detection method for low-affinity membrane protein interactions by baculoviral display.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2008-01-01
description BACKGROUND: Membrane protein interactions play an important role in cell-to-cell recognition in various biological activities such as in the immune or neural system. Nevertheless, there has remained the major obstacle of expression of the membrane proteins in their active form. Recently, we and other investigators found that functional membrane proteins express on baculovirus particles (budded virus, BV). In this study, we applied this BV display system to detect interaction between membrane proteins important for cell-to-cell interaction in immune system. METHODOLOGY/PRINCIPAL FINDINGS: We infected Sf9 cells with recombinant baculovirus encoding the T cell membrane protein CD2 or its ligand CD58 and recovered the BV. We detected specific interaction between CD2-displaying BV and CD58-displaying BV by an enzyme-linked immunosorbent assay (ELISA). Using this system, we also detected specific interaction between two other membrane receptor-ligand pairs, CD40-CD40 ligand (CD40L), and glucocorticoid-induced TNFR family-related protein (GITR)-GITR ligand (GITRL). Furthermore, we observed specific binding of BV displaying CD58, CD40L, or GITRL to cells naturally expressing their respective receptors by flowcytometric analysis using anti-baculoviral gp64 antibody. Finally we isolated CD2 cDNA from a cDNA expression library by magnetic separation using CD58-displaying BV and anti-gp64 antibody. CONCLUSIONS: We found the BV display system worked effectively in the detection of the interaction of membrane proteins. Since various membrane proteins and their oligomeric complexes can be displayed on BV in the native form, this BV display system should prove highly useful in the search for natural ligands or to develop screening systems for therapeutic antibodies and/or compounds.
url http://europepmc.org/articles/PMC2602974?pdf=render
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