Biosynthesis of elastin-like polypeptides and their applications in drug delivery

YANG Zhaoying; ZHANG Fan; GUO Jianwen; GAO Weiping

doi:10.12211/2096-8280.2021-094

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Biosynthesis of elastin-like polypeptides and their applications in drug delivery

Invited Review | 更新时间：2025-03-20

- Biosynthesis of elastin-like polypeptides and their applications in drug delivery
- Synthetic Biology Journal Vol. 3, Issue 4, Pages: 728-747(2022)
- 作者机构：
  
  1.北京大学跨学部生物医学工程系，北京 100191
  2.北京大学医学部医学技术研究院，北京 100191
- 作者简介：
- 基金信息：
- DOI：10.12211/2096-8280.2021-094
  CLC： Q81
- Received：27 September 2021，
  
  Revised：2021-11-11，
  
  Published：31 August 2022
- 稿件说明：
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杨兆颖，张帆，郭建文，高卫平. 类弹性蛋白多肽的生物合成及其药物递送应用［J］. 合成生物学， 2022， 3（4）： 728-747

YANG Zhaoying， ZHANG Fan， GUO Jianwen， GAO Weiping. Biosynthesis of elastin-like polypeptides and their applications in drug delivery［J］. Synthetic Biology Journal， 2022， 3（4）： 728-747
杨兆颖，张帆，郭建文，高卫平. 类弹性蛋白多肽的生物合成及其药物递送应用［J］. 合成生物学， 2022， 3（4）： 728-747 DOI： 10.12211/2096-8280.2021-094.

YANG Zhaoying， ZHANG Fan， GUO Jianwen， GAO Weiping. Biosynthesis of elastin-like polypeptides and their applications in drug delivery［J］. Synthetic Biology Journal， 2022， 3（4）： 728-747 DOI： 10.12211/2096-8280.2021-094.

摘要

类弹性蛋白多肽（elastin-like polypeptide，ELP）是一种衍生于天然弹性蛋白，可人工合成的多肽聚合物。ELP具有特殊的温度响应性，它会随温度的变化表现出可逆相转变行为，并且当它与其他小分子或多肽偶联时，该温敏特性可以被充分保留。借助基因工程可以人工合成ELP与ELP融合蛋白，精确调控ELP的结构与功能，在其序列中添加反应性氨基酸或多肽。同时，ELP由天然氨基酸组成，其生物相容性好，易于生物降解，免疫原性低，无毒性作用。基于以上优势，ELP已被广泛应用于蛋白的表达纯化、体外诊断、药物递送和组织工程等生物医药领域。本文结合国内外研究报道，简要介绍了ELP的设计原理、理化特性和生物合成方法，并列举了一些ELP应用于药物递送系统中有代表性的工作，最后总结了该研究领域面临的挑战和问题。

Abstract

Elastin-like polypeptides (ELPs) are artificially synthetic peptide polymers inspired by human elastin. ELPs are composed of repeat units of a Val-Pro-Gly-X-Gly

where X can be any amino acid except proline

and they can exhibit different biological functions along with X residue changes. ELPs are

thermally responsive and demonstrate lower critical solution temperature phase behavior. They are soluble at temperatures below a characteristic transition temperature (

) and reversibly phase separate into an insoluble

coacervate phase above the

. Moreover

the phase behavior is retained when the ELP is either genetically fused to peptides or covalently conjugated to small molecules

and this phase behavior can be adjusted through changing X residue and chain length of ELPs. As ELPs are typically produced from synthetic genes

the structure and function of ELPs can be accurately regulated through genetic engineering. The amino acids or peptides with reactive side chains can be incorporated into ELPs through recombination synthesis as well. This precision control over ELP is unmatched by synthetic polymers. Based on these properties

ELPs can be engineered to assemble into unique architecture and used as soluble macromolecular carriers

therapeutic drug depots

hyperthermia-targeted drug carriers and self-assembled micelles. Lastly

as ELPs are derived from natural protein sequences

they show desirable biological properties including excellent biocompatibility

low immunogenicity

and non-toxic effects. Due to these attributes

ELPs have been widely used in biomedical fields including protein expression and purification

in vitro

diagnosis

drug delivery and tissue engineering. By focusing primarily on applications of ELPs in drug delivery

this review introduces the design principles

physicochemical properties

biosynthetic methods of ELPs and ELP conjugates

as well as exemplifies representative applications of ELPs in drug delivery

as extending the half-life of drugs

tumor targeted delivery

local delivery

hyperthermia-targeted delivery and sustained released of the drugs

in vivo

. Challenges and problems faced in this emerging field are discussed at the end of this review.

关键词

Keywords

references

ADEPU S , RAMAKRISHNA S . Controlled drug delivery systems: Current status and future directions [J ] . Molecules , 2021 , 26 ( 19 ): 5905 .

MITHIEUX S M , WEISS A S . Elastin [M ] // San Diego: Academic Press Inc Elsevier Science , 2005 : 437 - 461 .

MCPHERSON D T , MORROW C , MINEHAN D S , et al . Production and purification of a recombinant elastomeric polypeptide, G-(VPGVG)19-VPGV, from Escherichia coli [J ] . Biotechnology Progress , 1992 , 8 ( 4 ): 347 - 352 .

MACEWAN S R , CHILKOTI A . Elastin-like polypeptides: biomedical applications of tunable biopolymers [J ] . Biopolymers , 2010 , 94 ( 1 ): 60 - 77 .

ZHAO B W , LI N K , YINGLING Y G , et al . LCST behavior is manifested in a single molecule: elastin-like polypeptide (VPGVG)N [J ] . Biomacromolecules , 2015 , 17 ( 1 ): 111 - 118 .

MEYER D E , CHILKOTI A . Quantification of the effects of chain length and concentration on the thermal behavior of elastin-like polypeptides [J ] . Biomacromolecules , 2004 , 5 ( 3 ): 846 - 851 .

NAIR L S , LAURENCIN C T . Biodegradable polymers as biomaterials [J ] . Progress in Polymer Science , 2007 , 32 ( 8/9 ): 762 - 798 .

CHILKOTI A , CHRISTENSEN T , MACKAY J A . Stimulus responsive elastin biopolymers: applications in medicine and biotechnology [J ] . Current Opinion in Chemical Biology , 2006 , 10 ( 6 ): 652 - 657 .

PRASAD K U , IQBAL M A , URRY D W . Utilization of 1-hydroxybenzotriazole in mixed anhydride coupling reactions [J ] . International Journal of Peptide and Protein Research , 1985 , 25 ( 4 ): 408 - 413 .

GUDA C , ZHANG X , MCPHERSON D T , et al . Hyper expression of an environmentally friendly synthetic polymer gene [J ] . Biotechnology Letters , 1995 , 17 ( 7 ): 745 - 750 .

MCPHERSON D T , XU J , URRY D W . Product purification by reversible phase transition following Escherichia coli expression of genes encoding up to 251 repeats of the elastomeric pentapeptide GVGVP [J ] . Protein Expression and Purification , 1996 , 7 ( 1 ): 51 - 57 .

MEYER D E , CHILKOTI A . Genetically encoded synthesis of protein-based polymers with precisely specified molecular weight and sequence by recursive directional ligation: examples from the elastin-like polypeptide system [J ] . Biomacromolecules , 2002 , 3 ( 2 ): 357 - 367 .

MCDANIEL J R , MACKAY J A , QUIROZ F G , et al . Recursive directional ligation by plasmid reconstruction allows rapid and seamless cloning of oligomeric genes [J ] . Biomacromolecules , 2010 , 11 ( 4 ): 944 - 952 .

AMIRAM M , QUIROZ F G , CALLAHAN D J , et al . A highly parallel method for synthesizing DNA repeats enables the discovery of “smart” protein polymers [J ] . Nature Materials , 2011 , 10 ( 2 ): 141 - 148 .

TANG N C , CHILKOTI A . Combinatorial codon scrambling enables scalable gene synthesis and amplification of repetitive proteins [J ] . Nature Materials , 2016 , 15 ( 4 ): 419 - 424 .

URRY D W . Free energy transduction in polypeptides and proteins based on inverse temperature transitions [J ] . Progress in Biophysics and Molecular Biology , 1992 , 57 ( 1 ): 23 - 57 .

URRY D W . Molecular machines: How motion and other functions of living organisms can result from reversible chemical changes [J ] . Angewandte Chemie International Edition in English , 1993 , 32 ( 6 ): 819 - 841 .

URRY D W . Physical chemistry of biological free energy transduction as demonstrated by elastic protein-based polymers [J ] . The Journal of Physical Chemistry B , 1997 , 101 ( 51 ): 11007 - 11028 .

MEYER D E , CHILKOTI A . Purification of recombinant proteins by fusion with thermally-responsive polypeptides [J ] . Nature Biotechnology , 1999 , 17 ( 11 ): 1112 - 1115 .

HASSOUNEH W , CHRISTENSEN T , CHILKOTI A . Elastin-like polypeptides as a purification tag for recombinant proteins [J ] . Current Protocols in Protein Science , 2010 , 61 ( 1 ): 6.11.1 - 6.11.16 .

LIM D W , TRABBIC-CARLSON K , MACKAY J A , et al . Improved non-chromatographic purification of a recombinant protein by cationic elastin-like polypeptides [J ] . Biomacromolecules , 2007 , 8 ( 5 ): 1417 - 1424 .

BOOTH J J , ABBOTT S , SHIMIZU S . Mechanism of hydrophobic drug solubilization by small molecule hydrotropes [J ] . The Journal of Physical Chemistry B , 2012 , 116 ( 51 ): 14915 - 14921 .

WANG Q Z . Recent advances in protein drug delivery [J ] . IOP Conference Series: Materials Science and Engineering , 2020 , 768 ( 5 ): 052055 .

LEADER B , BACA Q J , GOLAN D E . Protein therapeutics: a summary and pharmacological classification [J ] . Nature Reviews Drug Discovery , 2008 , 7 ( 1 ): 21 - 39 .

VERONESE F M , MERO A . The impact of PEGylation on biological therapies [J ] . BioDrugs , 2008 , 22 ( 5 ): 315 - 329 .

ABRAHAM S A , WATERHOUSE D N , MAYER L D , et al . The liposomal formulation of doxorubicin [J ] . Methods in Enzymology , 2005 , 391 : 71 - 97 .

DREHER M R , RAUCHER D , BALU N , et al . Evaluation of an elastin-like polypeptide-doxorubicin conjugate for cancer therapy [J ] . Journal of Controlled Release , 2003 , 91 ( 1/2 ): 31 - 43 .

FURGESON D Y , DREHER M R , CHILKOTI A . Structural optimization of a "smart" doxorubicin-polypeptide conjugate for thermally targeted delivery to solid tumors [J ] . Journal of Controlled Release , 2006 , 110 ( 2 ): 362 - 369 .

BIDWELL G L , DAVIS A N , FOKT I , et al . A thermally targeted elastin-like polypeptide-doxorubicin conjugate overcomes drug resistance [J ] . Investigational New Drugs , 2007 , 25 ( 4 ): 313 - 326 .

MOKTAN S , PERKINS E , KRATZ F , et al . Thermal targeting of an acid-sensitive doxorubicin conjugate of elastin-like polypeptide enhances the therapeutic efficacy compared with the parent compound in vivo [J ] . Molecular Cancer Therapeutics , 2012 , 11 ( 7 ): 1547 - 1556 .

ROUSSELLE C , CLAIR P , LEFAUCONNIER J M , et al . New advances in the transport of doxorubicin through the blood-brain barrier by a peptide vector-mediated strategy [J ] . Molecular Pharmacology , 2000 , 57 ( 4 ): 679 - 686 .

BIDWELL G L III , RAUCHER D . Cell penetrating elastin-like polypeptides for therapeutic peptide delivery [J ] . Advanced Drug Delivery Reviews , 2010 , 62 ( 15 ): 1486 - 1496 .

BIDWELL G L III , WHITTOM A A , THOMAS E , et al . A thermally targeted peptide inhibitor of symmetrical dimethylation inhibits cancer-cell proliferation [J ] . Peptides , 2010 , 31 ( 5 ): 834 - 841 .

MAINI R N , ELLIOTT M J , BRENNAN F M , et al . Beneficial effects of tumour necrosis factor-alpha (TNF-α) blockade in rheumatoid arthritis (RA) [J ] . Clinical and Experimental Immunology , 2013 , 101 ( 2 ): 207 - 212 .

BEUTLER B , MILSARK I W , CERAMI A C . Passive immunization against cachectin/tumor necrosis factor protects mice from lethal effect of endotoxin [J ] . Science , 1985 , 229 ( 4716 ): 869 - 871 .

VAN DULLEMEN H M , VAN DEVENTER S J H , HOMMES D W , et al . Treatment of Crohn's disease with anti-tumor necrosis factor chimeric monoclonal antibody (CA2) [J ] . Gastroenterology , 1995 , 109 ( 1 ): 129 - 135 .

FALVO J V , TSYTSYKOVA A V , GOLDFELD A E . Transcriptional control of the TNF gene [J ] . Current Directions in Autoimmunity , 2010 , 11 : 27 - 60 .

TSAI E Y , YIE J , THANOS D , et al . Cell-type-specific regulation of the human tumor necrosis factor alpha gene in B cells and T cells by NFATp and ATF-2/JUN [J ] . Molecular and Cellular Biology , 1996 , 16 ( 10 ): 5232 - 5244 .

高世勇 , 李丹 . 肿瘤坏死因子与癌症相关研究进展 [J ] . 中国药理学通报 , 2020 , 36 ( 9 ): 1209 - 1213 .

GAO S Y , LI D . Research advances in tumor necrosis factor and cancer [J ] . Chinese Pharmacological Bulletin , 2020 , 36 ( 9 ): 1209 - 1213 .

SMITH C A , FARRAH T , GOODWIN R G . The TNF receptor superfamily of cellular and viral proteins: activation, costimulation, and death [J ] . Cell , 1994 , 76 ( 6 ): 959 - 962 .

COPPIETERS K , DREIER T , SILENCE K , et al . Formatted anti-tumor necrosis factor alpha VHH proteins derived from camelids show superior potency and targeting to inflamed joints in a murine model of collagen-induced arthritis [J ] . Arthritis and Rheumatism , 2006 , 54 ( 6 ): 1856 - 1866 .

PLAGMANN I , CHALARIS A , KRUGLOV A A , et al . Transglutaminase-catalyzed covalent multimerization of Camelidae anti-human TNF single domain antibodies improves neutralizing activity [J ] . Journal of Biotechnology , 2009 , 142 ( 2 ): 170 - 178 .

CONRAD U , PLAGMANN I , MALCHOW S , et al . ELPylated anti-human TNF therapeutic single-domain antibodies for prevention of lethal septic shock [J ] . Plant Biotechnology Journal , 2011 , 9 ( 1 ): 22 - 31 .

HU J , WANG G L , LIU X Y , et al . Enhancing pharmacokinetics, tumor accumulation, and antitumor efficacy by elastin-like polypeptide fusion of interferon alpha [J ] . Advanced Materials , 2015 , 27 ( 45 ): 7320 - 7324 .

MIRANDA L P , WINTERS K A , GEGG C V , et al . Design and synthesis of conformationally constrained glucagon-like peptide-1 derivatives with increased plasma stability and prolonged in vivo activity [J ] . Journal of Medicinal Chemistry , 2008 , 51 ( 9 ): 2758 - 2765 .

桑延霞 . 胰高血糖素样肽1类似物长效化的策略 [J ] . 中国新药与临床杂志 , 2021 , 40 ( 7 ): 481 - 488 .

SANG Y X . Strategies for long-acting effect of glucagon-like peptide 1 analogs [J ] . Chinese Journal of New Drugs and Clinical Remedies , 2021 , 40 ( 7 ): 481 - 488 .

AMIRAM M , LUGINBUHL K M , LI X , et al . A depot-forming glucagon-like peptide-1 fusion protein reduces blood glucose for five days with a single injection [J ] . Journal of Controlled Release , 2013 , 172 ( 1 ): 144 - 151 .

MALM-ERJEFÄLT M , BJØRNSDOTTIR I , VANGGAARD J , et al . Metabolism and excretion of the once-daily human glucagon-like peptide-1 analog liraglutide in healthy male subjects and its in vitro degradation by dipeptidyl peptidase IV and neutral endopeptidase [J ] . Drug Metabolism and Disposition: the Biological Fate of Chemicals , 2010 , 38 ( 11 ): 1944 - 1953 .

WANG Z R , GUO J W , NING J , et al . One-month zero-order sustained release and tumor eradication after a single subcutaneous injection of interferon alpha fused with a body-temperature-responsive polypeptide [J ] . Biomaterials Science , 2018 , 7 ( 1 ): 104 - 112 .

LIANG P , WANG G H , LIU X Y , et al . Spatiotemporal combination of thermosensitive polypeptide fused interferon and temozolomide for post-surgical glioblastoma immunochemotherapy [J ] . Biomaterials , 2021 , 264 : 120447 .

WANG Z R , GUO J W , SUN J W , et al . Thermoresponsive and protease-cleavable interferon-polypeptide conjugates with spatiotemporally programmed two-step release kinetics for tumor therapy [J ] . Advanced Science , 2019 , 6 ( 16 ): 1900586 .

CHEVALIER X , GOUPILLE P , BEAULIEU A D , et al . Intraarticular injection of anakinra in osteoarthritis of the knee: A multicenter, randomized, double-blind, placebo-controlled study [J ] . Arthritis and Rheumatism , 2009 , 61 ( 3 ): 344 - 352 .

KIMMERLING K A , FURMAN B D , MANGIAPANI D S , et al . Sustained intra-articular delivery of IL-1RA from a thermally-responsive elastin-like polypeptide as a therapy for post-traumatic arthritis [J ] . European Cells & Materials , 2015 , 29 : 124 - 139 .

ADAMS S B , SHAMJI M F , NETTLES D L , et al . Sustained release of antibiotics from injectable and thermally responsive polypeptide depots [J ] . Journal of Biomedical Materials Research Part B , Applied Biomaterials, 2009 , 90 ( 1 ): 67 - 74 .

BETRE H , LIU W G , ZALUTSKY M R , et al . A thermally responsive biopolymer for intra-articular drug delivery [J ] . Journal of Controlled Release , 2006 , 115 ( 2 ): 175 - 182 .

ANAND P , THOMAS S G , KUNNUMAKKARA A B , et al . Biological activities of curcumin and its analogues (Congeners) made by man and Mother Nature [J ] . Biochemical Pharmacology , 2008 , 76 ( 11 ): 1590 - 1611 .

刘伟 , 顾秀竹 , 吴筱霓 , 等 . 姜黄素药理作用的研究进展 [J ] . 华西药学杂志 , 2021 , 36 ( 3 ): 336 - 340 .

LIU W , GU X Z , WU X N , et al . Research on the pharmacological actions of curcumin [J ] . West China Journal of Pharmaceutical Sciences , 2021 , 36 ( 3 ): 336 - 340 .

张洪英 . 中药姜黄的研究进展 [J ] . 菏泽医专学报 , 2001 , 13 ( 4 ): 84 - 87 .

ZHANG H Y . Research progress of traditional Chinese medicine turmeric [J ] . Journal of Heze Medical College , 2001 , 13 ( 4 ): 84 - 87 .

SINCLAIR S M , BHATTACHARYYA J , MCDANIEL J R , et al . A genetically engineered thermally responsive sustained release curcumin depot to treat neuroinflammation [J ] . Journal of Controlled Release , 2013 , 171 ( 1 ): 38 - 47 .

CARREIRA A C , ALVES G G , ZAMBUZZI W F , et al . Bone morphogenetic proteins: structure, biological function and therapeutic applications [J ] . Archives of Biochemistry and Biophysics , 2014 , 561 : 64 - 73 .

MIMATSU K , KISHI S , HASHIZUME Y . Experimental chronic compression on the spinal cord of the rabbit by ectopic bone formation in the ligamentum flavum with bone morphogenetic protein [J ] . Spinal Cord , 1997 , 35 ( 11 ): 740 - 746 .

MCCARTHY B , YUAN Y , KORIA P . Elastin-like-polypeptide based fusion proteins for osteogenic factor delivery in bone healing [J ] . Biotechnology Progress , 2016 , 32 ( 4 ): 1029 - 1037 .

DEWHIRST M W , PROSNITZ L , THRALL D , et al . Hyperthermic treatment of malignant diseases: current status and a view toward the future [J ] . Seminars in Oncology , 1997 , 24 ( 6 ): 616 - 625 .

FEYERABEND T , STEEVES R , WIEDEMANN G J , et al . Rationale and clinical status of local hyperthermia, radiation, and chemotherapy in locally advanced malignancies [J ] . Anticancer Research , 1997 , 17 ( 4B ): 2895 - 2897 .

ISSELS R . Hyperthermia combined with chemotherapy-biological rationale, clinical application, and treatment results [J ] . Oncology Research and Treatment , 1999 , 22 ( 5 ): 374 - 381 .

RAUCHER D , CHILKOTI A . Enhanced uptake of a thermally responsive polypeptide by tumor cells in response to its hyperthermia-mediated phase transition [J ] . Cancer Research , 2001 , 61 ( 19 ): 7163 - 7170 .

MEYER D E , KONG G A , DEWHIRST M W , et al . Targeting a genetically engineered elastin-like polypeptide to solid tumors by local hyperthermia [J ] . Cancer Research , 2001 , 61 ( 4 ): 1548 - 1554 .

WHITESIDES G M , MATHIAS J P , SETO C T . Molecular self-assembly and nanochemistry: a chemical strategy for the synthesis of nanostructures [J ] . Science , 1991 , 254 ( 5036 ): 1312 - 1319 .

RODRÍGUEZ-HERNÁNDEZ J , CHÉCOT F , GNANOU Y , et al . Toward "smart" nano-objects by self-assembly of block copolymers in solution [J ] . Progress in Polymer Science , 2005 , 30 ( 7 ): 691 - 724 .

DREHER M R , SIMNICK A J , FISCHER K , et al . Temperature triggered self-assembly of polypeptides into multivalent spherical micelles [J ] . Journal of the American Chemical Society , 2008 , 130 ( 2 ): 687 - 694 .

杨国新 , 侯佳男 , 胡学军 , 等 . 自组装ELP多肽的从头设计及其在生物医药领域中的应用进展 [J ] . 生命的化学 , 2021 , 41 ( 2 ): 296 - 305 .

YANG G X , HOU J N , HU X J , et al . De novo design of self-assembled ELP peptides and their applications in biomedicine [J ] . Chemistry of Life , 2021 , 41 ( 2 ): 296 - 305 .

ABDELGHANI M , SHAO J X , LE D H T , et al . Self-assembly or coassembly of multiresponsive histidine-containing elastin-like polypeptide block copolymers [J ] . Macromolecular Bioscience , 2021 , 21 ( 6 ): e2100081 .

WANG Z R , GUO J W , LIU X Y , et al . Temperature-triggered micellization of interferon alpha-diblock copolypeptide conjugate with enhanced stability and pharmacology [J ] . Journal of Controlled Release , 2020 , 328 : 444 - 453 .

SIMAMORA P , ALVAREZ J M , YALKOWSKY S H . Solubilization of rapamycin [J ] . International Journal of Pharmaceutics , 2001 , 213 ( 1/2 ): 25 - 29 .

SHI P , ALURI S , LIN Y A , et al . Elastin-based protein polymer nanoparticles carrying drug at both corona and core suppress tumor growth in vivo [J ] . Journal of Controlled Release , 2013 , 171 ( 3 ): 330 - 338 .

郑鹏生 , 冀静 . mTOR信号通路与肿瘤的研究进展 [J ] . 西安交通大学学报(医学版) , 2010 , 31 ( 1 ): 1 - 9 .

ZHENG P S , JI J . Advance in research on the relationship between mTOR signaling pathway and tumors [J ] . Journal of Xi'an Jiaotong University (Medical Sciences) , 2010 , 31 ( 1 ): 1 - 9 .

MCDANIEL J R , BHATTACHARYYA J , VARGO K B , et al . Self-assembly of thermally responsive nanoparticles of a genetically encoded peptide polymer by drug conjugation [J ] . Angewandte Chemie International Edition , 2013 , 52 ( 6 ): 1683 - 1687 .

WANG Z R , HE Q , ZHAO W G , et al . Tumor-homing, pH- and ultrasound-responsive polypeptide-doxorubicin nanoconjugates overcome doxorubicin resistance in cancer therapy [J ] . Journal of Controlled Release , 2017 , 264 : 66 - 75 .

DHARAP S S , WANG Y , CHANDNA P , et al . Tumor-specific targeting of an anticancer drug delivery system by LHRH peptide [J ] . Proceedings of the National Academy of Sciences of the United States of America , 2005 , 102 ( 36 ): 12962 - 12967 .

BHATTACHARYYA J , WEITZHANDLER I , HO S B , et al . Encapsulating a hydrophilic chemotherapeutic into rod-like nanoparticles of a genetically encoded asymmetric triblock polypeptide improves its efficacy [J ] . Advanced Functional Materials , 2017 , 27 ( 12 ): 1605421 .

LUGINBUHL K M , MOZHDEHI D , DZURICKY M , et al . Recombinant synthesis of hybrid lipid-peptide polymer fusions that self-assemble and encapsulate hydrophobic drugs [J ] . Angewandte Chemie International Edition , 2017 , 56 ( 45 ): 13979 - 13984 .

SUN M M , GUO J W , HAO H J , et al . Tumour-homing chimeric polypeptide-conjugated polypyrrole nanoparticles for imaging-guided synergistic photothermal and chemical therapy of cancer [J ] . Theranostics , 2018 , 8 ( 10 ): 2634 - 2645 .

黄晚秋 , 高苗苗 , 窦红静 . 聚吡咯及其纳米复合材料在光热治疗领域的应用 [J ] . 化学进展 , 2020 , 32 ( 4 ): 371 - 380 .

HUANG W Q , GAO M M , DOU H J . Polypyrrole and its nanocomposites applied in photothermal therapy [J ] . Progress in Chemistry , 2020 , 32 ( 4 ): 371 - 380 .

PALLAVICINI P , DONÀ A , CASU A , et al . Triton X-100 for three-plasmon gold nanostars with two photothermally active NIR (near IR) and SWIR (short-wavelength IR) channels [J ] . Chemical Communications , 2013 , 49 ( 56 ): 6265 - 6267 .

LIU X S , HUANG N , LI H , et al . Multidentate polyethylene glycol modified gold nanorods for in vivo near-infrared photothermal cancer therapy [J ] . ACS Applied Materials & Interfaces , 2014 , 6 ( 8 ): 5657 - 5668 .

KHLEBTSOV N , BOGATYREV V , DYKMAN L , et al . Analytical and theranostic applications of gold nanoparticles and multifunctional nanocomposites [J ] . Theranostics , 2013 , 3 ( 3 ): 167 - 180 .

GRABINSKI C , SCHAEUBLIN N , WIJAYA A , et al . Effect of gold nanorod surface chemistry on cellular response [J ] . ACS Nano , 2011 , 5 ( 4 ): 2870 - 2879 .

WANG S T , CHEN K J , WU T H , et al . Photothermal effects of supramolecularly assembled gold nanoparticles for the targeted treatment of cancer cells [J ] . Angewandte Chemie International Edition , 2010 , 49 ( 22 ): 3777 - 3781 .

SUN M M , PENG D , HAO H J , et al . Thermally triggered in situ assembly of gold nanoparticles for cancer multimodal imaging and photothermal therapy [J ] . ACS Applied Materials & Interfaces , 2017 , 9 ( 12 ): 10453 - 10460 .

BETRE H , SETTON L A , MEYER D E , et al . Characterization of a genetically engineered elastin-like polypeptide for cartilaginous tissue repair [J ] . Biomacromolecules , 2002 , 3 ( 5 ): 910 - 916 .

URRY D W , HAYNES B , ZHANG H , et al . Mechanochemical coupling in synthetic polypeptides by modulation of an inverse temperature transition [J ] . Proceedings of the National Academy of Sciences of the United States of America , 1988 , 85 ( 10 ): 3407 - 3411 .

TRABBIC-CARLSON K , SETTON L A , CHILKOTI A . Swelling and mechanical behaviors of chemically cross-linked hydrogels of elastin-like polypeptides [J ] . Biomacromolecules , 2003 , 4 ( 3 ): 572 - 580 .

HRABCHAK C , ROULEAU J , MOSS I , et al . Assessment of biocompatibility and initial evaluation of genipin cross-linked elastin-like polypeptides in the treatment of an osteochondral knee defect in rabbits [J ] . Acta Biomaterialia , 2010 , 6 ( 6 ): 2108 - 2115 .

SUN F , ZHANG W B , MAHDAVI A , et al . Synthesis of bioactive protein hydrogels by genetically encoded SpyTag-SpyCatcher chemistry [J ] . Proceedings of the National Academy of Sciences of the United States of America , 2014 , 111 ( 31 ): 11269 - 11274 .

PAL P , NGUYEN Q C , BENTON A H , et al . Drug-loaded elastin-like polypeptide-collagen hydrogels with high modulus for bone tissue engineering [J ] . Macromolecular Bioscience , 2019 , 19 ( 9 ): e1900142 .

ZHANG W B , SUN F , TIRRELL D A , et al . Controlling macromolecular topology with genetically encoded SpyTag-SpyCatcher chemistry [J ] . Journal of the American Chemical Society , 2013 , 135 ( 37 ): 13988 - 13997 .

WANG X W , ZHANG W B . Cellular synthesis of protein catenanes [J ] . Angewandte Chemie International Edition , 2016 , 55 ( 10 ): 3442 - 3446 .

LIU D , WU W H , LIU Y J , et al . Topology engineering of proteins in vivo using genetically encoded, mechanically interlocking SpyX modules for enhanced stability [J ] . ACS Central Science , 2017 , 3 ( 5 ): 473 - 481 .

DA X D , ZHANG W B . Active template synthesis of protein heterocatenanes [J ] . Angewandte Chemie International Edition , 2019 , 58 ( 32 ): 11097 - 11104 .

ROSANO G L , CECCARELLI E A . Recombinant protein expression in Escherichia coli : advances and challenges [J ] . Frontiers in Microbiology , 2014 , 5 : 172 .

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School of Biomedical Engineering （Suzhou）， Division of Life Science and Medicine， University of Science and Technology of China

The Department of Chemistry， Tsinghua University

The Changchun Institute of Applied Chemistry （CIAC）， Chinese Academy of Sciences

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