Abstract

Ultrasound (US) imaging is a widely used imaging technique. The use of US contrast agents such as microbubbles, which consist of phospholipids and are filled with perfluorocarbon gases, has become an indispensable component of clinical US imaging, while molecular US imaging has recently attracted significant attention in combination with efficient diagnostics. The avidin–biotin interaction method is frequently used to tether antibodies to microbubbles, leading to the development of a molecular targeting US imaging agent. However, avidin still has limitations such as immunogenicity. We previously reported that lipid-based nanobubbles (NBs) containing perfluorocarbon gas are suitable for US imaging and gene delivery. In this paper, we report on the development of a novel antibody modification method for NBs using Fc-region-binding polypeptides derived from protein A/G. First, we prepared anti-CD146 antibody-modified NBs using this polypeptide, resulting in high levels of attachment to human umbilical vein endothelial cells expressing CD146. To examine their targeting ability and US imaging capability, the NBs were administered to tumor-bearing mice. The contrast imaging of antibody-modified NBs was shown to be prolonged compared with that of non-labeled NBs. Thus, this antibody modification method using an Fc-binding polypeptide may be a feasible tool for developing a next-generation antibody-modified US imaging agent.

Highlights

  • Ultrasound (US) imaging is a frequently used diagnostic technique that offers high spatial resolution, allows for real-time imaging, and combines the advantages of non-invasiveness without the use of ionizing radiation and at a low cost [1,2]

  • Fc-A59 polypeptide was produced for modification of the anti-CD146 antibody based on previous reports [26]

  • The Fc-G67 polypeptide was produced for modification of the anti-HER2 antibody (4D5-Fc) based on previous reports [27]

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Summary

Introduction

Ultrasound (US) imaging is a frequently used diagnostic technique that offers high spatial resolution, allows for real-time imaging, and combines the advantages of non-invasiveness without the use of ionizing radiation and at a low cost [1,2]. US contrast agents are gas-filled, echogenic microbubbles that remain exclusively in the vascular compartment [2]. The application of microbubbles has has brPmeheiacccremornoamcbteluueytbiacbbsnle2e0eis1nn9d,tr1hie1sa,pptxoeFrrOnetRsemadPabEi[Eln4eR]cR.eoExMVmcIlEiupcWsroiovnbeeluynbt bionlfescthlaienidicvaianlscUeunSlahriamncacogimninpggatrht[m3e]e,snpatnecd[i2fim].ciotTlyheecaunaldaprpseilmincasatigito2iivnnoifgtoy1v0f oiaf. Atinmionntgertahcetsieon has oftentabrgeeetninagdsotrpatteegdietso, amnotidboifdyiems hicarvoebbuebenbluessewd aitshaatanrtgibetoindgiems.oHietoywofemveicr,roabvuidbbinless,tialnl dhathseliamviidtiant–ions in its ubseioftuinlnienstesrbacetcioanusheasoof ftthene ibmeemn uadnoopgteednitcoitmyoodfifsytrmepictraovbiudbinbleins whuithmaanntisb[o1d2i]e.s.THhoewreefvoerre,,atvhiedicnlinical applsitciallthioans loimf iatavtiidonins–ibniiotstiunseinfutelnreascstiboencasuyssetoefmthseisimdmiffiuncougltenaitciptyreosfesntrte[p1t3a]v.idCinoinnsehquumeanntsly[1, 2a].novel antibTohderyefmoroed, itfihceactliionniciasl raepqpuliicraetdiofnorofapavpildicina–tiboiontsinininctleinraicctaiol nsestytisntegms.s is difficult at present [13]. Fc-bipnodlyinpgepptiodleyspedpetriidveesddferroimvedprforoteminpAro/tGeinanAd/Gdaevnedlodpeevdeloanpteibdoadnyt-imbooddiyfi-emdodNiBfiseduNsinBgs uthsiensge these polyppoelpytpidepetsid(Fesig(Fuirgeu1re: 1S:cShcehmemataitcicoofftthhee ddeevveellooppmmeennt tofoafnatnibtoibdoyd-my-omdiofideidfiNedBsNuBsisnugsainnFgca-bninFdci-nbginding polyppoelpyptiedpet)id. SAsshsohwownnininFFigiguurree 11,, wwee ppllaannnneeddthtehededveevloeplompemntenoft tohfetahnetiabnodtiybomdoydimficoadtiiofincation methmcaoendthbfoeodrmfNoodrBiNsfieBudssiounnsginliagpnoasFnocmF-bce-isbn/iNdndBinisngvgipapootlhlyyepppeeoppltytiidpdeeep..BtiBydyeu.usBisneicgnagaunsaeFnCcF-Dbci1-n4bd6iinnwdgaisnpoegxlypppeoeclptyetpdidetepo,tabidneteai,bnaoodnviteiebsl odies can benedmotohdeliifiael dbioomn alirpkoersothmatesa/cNtsBassvaiacoth-reecpeopltyorpefoprtivdaes.cuBlearcaeunsdeotChDeli1a4l 6grwowasthexfapcetcotrerdecteopbtoer-a2novel endo(VthEeGliFaRl -b2)ioimn aturkmeorrthanagtiaogctesneassisa[2c5o]-,rewceepcthoorsefoCrDv1a4s6cualsara etnumdootrh-tealrigaeltignrgowmtohlefcaucletofrorretcheeptor-2 (VEGuFltRra-s2o)uindtuimaogriannggaigoegnetn.

Production of Fc-Binding Polypeptides
Generation of an Antiserum for Mouse CD146 and 4D5-Fc Antibodies
Preparation of Antibody-Modified Liposomes and NBs
Cells and Tumor Model Mice
Fluorescent Microscopic Analysis
In Vivo US Imaging Analysis
Results and Discussion
Full Text
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