TY - JOUR
T1 - Bilingual Peptide Nucleic Acids
T2 - Encoding the Languages of Nucleic Acids and Proteins in a Single Self-Assembling Biopolymer
AU - Swenson, Colin S.
AU - Velusamy, Arventh
AU - Argueta-Gonzalez, Hector S.
AU - Heemstra, Jennifer M.
N1 - Funding Information:
This work was supported by the National Science Foundation (DMR 1822262 J.M.H.). The authors also acknowledge the Robert P. Apkarian Integrated Electron Microscopy Core and NMR Research Center at Emory University for access to instruments and technical assistance and Mr. Steve Knutson for helpful input on the writing of this manuscript.
Funding Information:
This work was supported by the National Science Foundation (DMR 1822262 J.M.H.). The authors also acknowledge the Robert P. Apkarian Integrated Electron Microscopy Core and NMR Research Center at Emory University for access to instruments and technical assistance and Mr. Steve Knutson for helpful input on the writing of this manuscript.
Publisher Copyright:
Copyright © 2019 American Chemical Society.
PY - 2019/12/4
Y1 - 2019/12/4
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=85075774187&partnerID=8YFLogxK
U2 - 10.1021/jacs.9b09146
DO - 10.1021/jacs.9b09146
M3 - Article
C2 - 31711285
AN - SCOPUS:85075774187
SN - 0002-7863
VL - 141
SP - 19038
EP - 19047
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
IS - 48
ER -