Bilingual Peptide Nucleic Acids: Encoding the Languages of Nucleic Acids and Proteins in a Single Self-Assembling Biopolymer

被引:46
作者
Swenson, Colin S. [1 ]
Velusamy, Arventh [1 ]
Argueta-Gonzalez, Hector S. [1 ]
Heemstra, Jennifer M. [1 ]
机构
[1] Emory Univ, Dept Chem, 1515 Pierce Dr, Atlanta, GA 30322 USA
基金
美国国家科学基金会;
关键词
DNA-BINDING; GAMMA-PNA; FLUOROPHORES; AMPHIPHILES; STABILITY; MOLECULE; MONOMERS;
D O I
10.1021/jacs.9b09146
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Nucleic acids and proteins are the fundamental biopolymers that support all life on Earth. Nucleic acids store large amounts of information in nucleobase sequences while peptides and proteins utilize diverse amino acid functional groups to adopt complex structures and perform wide-ranging activities. Although nature has evolved machinery to read the nucleic acid code and translate it into amino acid code, the extant biopolymers are restricted to encoding amino acid or nucleotide sequences separately, limiting their potential applications in medicine and biotechnology. Here we describe the design, synthesis, and stimuli-responsive assembly behavior of a bilingual biopolymer that integrates both amino acid and nucleobase sequences into a single peptide nucleic acid (PNA) scaffold to enable tunable storage and retrieval of tertiary structural behavior and programmable molecular recognition capabilities. Incorporation of a defined sequence of amino acid side-chains along the PNA backbone yields amphiphiles having a "protein code" that directs self-assembly into micellar architectures in aqueous conditions. However, these amphiphiles also carry a "nucleotide code" such that subsequent introduction of a complementary RNA strand induces a sequence-specific disruption of assemblies through hybridization. Together, these properties establish bilingual PNA as a powerful biopolymer that combines two information systems to harness structural responsiveness and sequence recognition. The PNA scaffold and our synthetic system are highly generalizable, enabling fabrication of a wide array of user-defined peptide and nucleotide sequence combinations for diverse future biomedical and nanotechnology applications.
引用
收藏
页码:19038 / 19047
页数:10
相关论文
共 41 条
[1]  
[Anonymous], 2018, NAT REV MAT
[2]  
DECOSTA NTS, 2013, PLOS ONE, V0008
[3]   STABILITY OF PEPTIDE NUCLEIC-ACIDS IN HUMAN SERUM AND CELLULAR-EXTRACTS [J].
DEMIDOV, VV ;
POTAMAN, VN ;
FRANKKAMENETSKII, MD ;
EGHOLM, M ;
BUCHARD, O ;
SONNICHSEN, SH ;
NIELSEN, PE .
BIOCHEMICAL PHARMACOLOGY, 1994, 48 (06) :1310-1313
[4]   Characterizing Manufactured Nanoparticles in the Environment: Multimethod Determination of Particle Sizes [J].
Domingos, Rute F. ;
Baalousha, Mohamed A. ;
Ju-Nam, Yon ;
Reid, M. Marcia ;
Tufenkji, Nathalie ;
Lead, Jamie R. ;
Leppard, Gary G. ;
Wilkinson, Kevin J. .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2009, 43 (19) :7277-7284
[5]   Single nucleotide specific detection of DNA by native chemical ligation of fluorescence labeled PNA-probes [J].
Dose, Christian ;
Seitz, Oliver .
BIOORGANIC & MEDICINAL CHEMISTRY, 2008, 16 (01) :65-77
[6]   A simple γ-backbone modification preorganizes peptide nucleic acid into a helical structure [J].
Dragulescu-Andrasi, Anca ;
Rapireddy, Srinivas ;
Frezza, Brian M. ;
Gayathri, Chakicherla ;
Gil, Roberto R. ;
Ly, Danith H. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2006, 128 (31) :10258-10267
[7]   PEPTIDE NUCLEIC-ACID (PNA) WITH A CHIRAL BACKBONE BASED ON ALANINE [J].
DUEHOLM, KL ;
PETERSEN, KH ;
JENSEN, DK ;
EGHOLM, M ;
NIELSEN, PE ;
BUCHARDT, O .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 1994, 4 (08) :1077-1080
[8]   PNA HYBRIDIZES TO COMPLEMENTARY OLIGONUCLEOTIDES OBEYING THE WATSON-CRICK HYDROGEN-BONDING RULES [J].
EGHOLM, M ;
BUCHARDT, O ;
CHRISTENSEN, L ;
BEHRENS, C ;
FREIER, SM ;
DRIVER, DA ;
BERG, RH ;
KIM, SK ;
NORDEN, B ;
NIELSEN, PE .
NATURE, 1993, 365 (6446) :566-568
[9]   PEPTIDE NUCLEIC-ACIDS (PNA) - OLIGONUCLEOTIDE ANALOGS WITH AN ACHIRAL PEPTIDE BACKBONE [J].
EGHOLM, M ;
BUCHARDT, O ;
NIELSEN, PE ;
BERG, RH .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1992, 114 (05) :1895-1897
[10]   Synthesis of γ-substituted peptide nucleic acids: A new place to attach fluorophores without affecting DNA binding [J].
Englund, EA ;
Appella, DH .
ORGANIC LETTERS, 2005, 7 (16) :3465-3467