Dual pH- and temperature-responsive protein nanoparticles
被引:29
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作者:
Matsumoto, Nicholas M.
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Univ Calif Los Angeles, Dept Chem & Biochem, Los Angeles, CA 90095 USA
Univ Calif Los Angeles, Calif Nanosyst Inst, Los Angeles, CA 90095 USAUniv Calif Los Angeles, Dept Chem & Biochem, Los Angeles, CA 90095 USA
Matsumoto, Nicholas M.
[1
,2
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Buchman, George W.
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Paragon Bioserv Inc, Baltimore, MD 21201 USAUniv Calif Los Angeles, Dept Chem & Biochem, Los Angeles, CA 90095 USA
Buchman, George W.
[3
]
Rome, Leonard H.
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Univ Calif Los Angeles, Calif Nanosyst Inst, Los Angeles, CA 90095 USA
Univ Calif Los Angeles, David Geffen Sch Med, Dept Biol Chem, Los Angeles, CA 90095 USAUniv Calif Los Angeles, Dept Chem & Biochem, Los Angeles, CA 90095 USA
Rome, Leonard H.
[2
,4
]
Maynard, Heather D.
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Univ Calif Los Angeles, Dept Chem & Biochem, Los Angeles, CA 90095 USA
Univ Calif Los Angeles, Calif Nanosyst Inst, Los Angeles, CA 90095 USAUniv Calif Los Angeles, Dept Chem & Biochem, Los Angeles, CA 90095 USA
Maynard, Heather D.
[1
,2
]
机构:
[1] Univ Calif Los Angeles, Dept Chem & Biochem, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, Calif Nanosyst Inst, Los Angeles, CA 90095 USA
[3] Paragon Bioserv Inc, Baltimore, MD 21201 USA
[4] Univ Calif Los Angeles, David Geffen Sch Med, Dept Biol Chem, Los Angeles, CA 90095 USA
Multiply responsive protein nanoparticles are interesting for a variety of applications. Herein, we describe the synthesis of a vault nanoparticle that responds to both temperature and pH. Specifically, poly(N-isopropylacrylamide-co-acrylic acid) with a pyridyl disulfide end group was prepared by reversible addition-fragmentation chain transfer (RAFT) polymerization. The polymer had a lower critical solution temperature (LCST) of 31.9 degrees C at pH 5, 44.0 degrees C at pH 6 and above 60 degrees C at pH 7. The polymer was conjugated to human major vault protein (hMVP), and the resulting nanoparticle was analyzed by UV-Vis, dynamic light scattering (DLS) and electron microscopy. The data demonstrated that the poly(N-isopropylacrylamide-co-acrylic acid)-vault conjugate did not respond to temperatures below 60 degrees C at pH 7, while the nanoparticles reversibly aggregated at pH 6. Furthermore, it was shown that the vault nanoparticle structure remained intact for at least three heat and cooling cycles. Thus, these dually responsive nanoparticles may serve as a platform for drug delivery and other applications. (C) 2015 Elsevier Ltd. All rights reserved.
机构:
Univ South Australia, Future Ind Inst, Mawson Lakes, SA 5095, AustraliaFlinders Univ S Australia, Coll Med & Publ Hlth, Bedford Pk, SA 5042, Australia
Haidari, Hanif
Vasilev, Krasimir
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Flinders Univ S Australia, Coll Med & Publ Hlth, Bedford Pk, SA 5042, AustraliaFlinders Univ S Australia, Coll Med & Publ Hlth, Bedford Pk, SA 5042, Australia
机构:E China Univ Sci & Technol, Key Lab Adv Mat, Shanghai 200237, Peoples R China
Han, Xia
Zhang, Xuxia
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机构:E China Univ Sci & Technol, Key Lab Adv Mat, Shanghai 200237, Peoples R China
Zhang, Xuxia
Zhu, Hongfan
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机构:E China Univ Sci & Technol, Key Lab Adv Mat, Shanghai 200237, Peoples R China
Zhu, Hongfan
Yin, Quanyi
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机构:E China Univ Sci & Technol, Key Lab Adv Mat, Shanghai 200237, Peoples R China
Yin, Quanyi
Liu, HongLai
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机构:
E China Univ Sci & Technol, Key Lab Adv Mat, Shanghai 200237, Peoples R ChinaE China Univ Sci & Technol, Key Lab Adv Mat, Shanghai 200237, Peoples R China
Liu, HongLai
Hu, Ying
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机构:E China Univ Sci & Technol, Key Lab Adv Mat, Shanghai 200237, Peoples R China