Selection for constrained peptides that bind to a single target protein
Published 2021 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Selection for constrained peptides that bind to a single target protein
Authors
Keywords
-
Journal
Nature Communications
Volume 12, Issue 1, Pages -
Publisher
Springer Science and Business Media LLC
Online
2021-11-05
DOI
10.1038/s41467-021-26350-4
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- GRINS: Genetic elements that recode assembly-line polyketide synthases and accelerate their diversification
- (2021) Aleksandra Nivina et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Detecting protein-protein interaction based on protein fragment complementation assay
- (2020) Tianwen Wang et al. CURRENT PROTEIN & PEPTIDE SCIENCE
- Evolution-guided discovery of antibiotics that inhibit peptidoglycan remodelling
- (2020) Elizabeth J. Culp et al. NATURE
- MOrPH-PhD: An Integrated Phage Display Platform for the Discovery of Functional Genetically Encoded Peptide Macrocycles
- (2020) Andrew E. Owens et al. ACS Central Science
- Structure, Function, and Antigenicity of the SARS-CoV-2 Spike Glycoprotein
- (2020) Alexandra C. Walls et al. CELL
- Natural Products as Sources of New Drugs over the Nearly Four Decades from 01/1981 to 09/2019
- (2020) David J. Newman et al. JOURNAL OF NATURAL PRODUCTS
- Structure of the SARS-CoV-2 spike receptor-binding domain bound to the ACE2 receptor
- (2020) Jun Lan et al. NATURE
- A noncompeting pair of human neutralizing antibodies block COVID-19 virus binding to its receptor ACE2
- (2020) Yan Wu et al. SCIENCE
- A highly conserved cryptic epitope in the receptor binding domains of SARS-CoV-2 and SARS-CoV
- (2020) Meng Yuan et al. SCIENCE
- Split Intein-Mediated Protein Ligation for detecting protein-protein interactions and their inhibition
- (2020) Zhong Yao et al. Nature Communications
- An expanded library of orthogonal split inteins enables modular multi-peptide assemblies
- (2020) Filipe Pinto et al. Nature Communications
- Genomic discovery of an evolutionarily programmed modality for small-molecule targeting of an intractable protein surface
- (2020) Uddhav K. Shigdel et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Broad neutralization of SARS-related viruses by human monoclonal antibodies
- (2020) Anna Z. Wec et al. SCIENCE
- A panel of human neutralizing mAbs targeting SARS-CoV-2 spike at multiple epitopes
- (2020) Tal Noy-Porat et al. Nature Communications
- GTP-State-Selective Cyclic Peptide Ligands of K-Ras(G12D) Block Its Interaction with Raf
- (2020) Ziyang Zhang et al. ACS Central Science
- Designing stapled peptides to inhibit protein‐protein interactions: An analysis of successes in a rapidly changing field
- (2020) Marie T. J. Bluntzer et al. Peptide Science
- High-Contrast CXCR4-Targeted 18F-PET Imaging Using a Potent and Selective Antagonist
- (2020) Daniel Kwon et al. MOLECULAR PHARMACEUTICS
- Bioinformatic Mapping of Radical S-Adenosylmethionine-Dependent Ribosomally Synthesized and Post-Translationally Modified Peptides Identifies New Cα, Cβ, and Cγ-Linked Thioether-Containing Peptides
- (2019) Graham A. Hudson et al. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
- Macrocyclic peptide-based inhibition and imaging of hepatocyte growth factor
- (2019) Katsuya Sakai et al. Nature Chemical Biology
- Assessing the Flexibility of the Prochlorosin 2.8 Scaffold for Bioengineering Applications
- (2019) Julian D. Hegemann et al. ACS Synthetic Biology
- Reconstitution and Substrate Specificity of the Thioether-Forming Radical S-Adenosylmethionine Enzyme in Freyrasin Biosynthesis
- (2019) Timothy W. Precord et al. ACS Chemical Biology
- A Genetically Encoded, Phage-Displayed Cyclic-Peptide Library
- (2019) Xiaoshan Shayna Wang et al. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
- Structure–activity relationship and conformational studies of the natural product cyclic depsipeptides YM-254890 and FR900359
- (2018) Hang Zhang et al. EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY
- Engineered promoters enable constant gene expression at any copy number in bacteria
- (2018) Thomas H Segall-Shapiro et al. NATURE BIOTECHNOLOGY
- A lanthipeptide library used to identify a protein–protein interaction inhibitor
- (2018) Xiao Yang et al. Nature Chemical Biology
- Cyclization of peptides with two chemical bridges affords large scaffold diversities
- (2018) Sangram S. Kale et al. Nature Chemistry
- Development and Application of Yeast and Phage Display of Diverse Lanthipeptides
- (2018) Kenton J. Hetrick et al. ACS Central Science
- Constrained peptides' time to shine?
- (2018) Chris Morrison NATURE REVIEWS DRUG DISCOVERY
- Escherichia coli “Marionette” strains with 12 highly optimized small-molecule sensors
- (2018) Adam J. Meyer et al. Nature Chemical Biology
- Rapamycin-inspired macrocycles with new target specificity
- (2018) Zufeng Guo et al. Nature Chemistry
- Double-slit photoelectron interference in strong-field ionization of the neon dimer
- (2018) Maksim Kunitski et al. Nature Communications
- Directing evolution: the next revolution in drug discovery?
- (2017) Andrew M. Davis et al. NATURE REVIEWS DRUG DISCOVERY
- Evolutionary radiation of lanthipeptides in marine cyanobacteria
- (2017) Andres Cubillos-Ruiz et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- UCSF ChimeraX: Meeting modern challenges in visualization and analysis
- (2017) Thomas D. Goddard et al. PROTEIN SCIENCE
- Phage display and selection of lanthipeptides on the carboxy-terminus of the gene-3 minor coat protein
- (2017) Johannes H. Urban et al. Nature Communications
- Chimeric Leader Peptides for the Generation of Non-Natural Hybrid RiPP Products
- (2017) Brandon J. Burkhart et al. ACS Central Science
- Discovery and optimization of peptide macrocycles
- (2016) Andrew M. White et al. Expert Opinion on Drug Discovery
- Induced protein degradation: an emerging drug discovery paradigm
- (2016) Ashton C. Lai et al. NATURE REVIEWS DRUG DISCOVERY
- Evolving Orthogonal Suppressor tRNAs To Incorporate Modified Amino Acids
- (2016) Andre C. Maranhao et al. ACS Synthetic Biology
- Construction of Lasso Peptide Fusion Proteins
- (2015) Chuhan Zong et al. ACS Chemical Biology
- Semi-synthesis of cyclosporins
- (2015) Michael Peel et al. BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS
- The structural biology of biosynthetic megaenzymes
- (2015) Kira J Weissman Nature Chemical Biology
- Split-luciferase complementary assay: applications, recent developments, and future perspectives
- (2014) Taha Azad et al. ANALYTICAL AND BIOANALYTICAL CHEMISTRY
- Lassomycin, a Ribosomally Synthesized Cyclic Peptide, Kills Mycobacterium tuberculosis by Targeting the ATP-Dependent Protease ClpC1P1P2
- (2014) Ekaterina Gavrish et al. CHEMISTRY & BIOLOGY
- Structural investigation of ribosomally synthesized natural products by hypothetical structure enumeration and evaluation using tandem MS
- (2014) Q. Zhang et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Adhiron: a stable and versatile peptide display scaffold for molecular recognition applications
- (2014) Christian Tiede et al. PROTEIN ENGINEERING DESIGN & SELECTION
- Nature's recipe for splitting inteins
- (2014) A. S. Aranko et al. PROTEIN ENGINEERING DESIGN & SELECTION
- ChemCalc: A Building Block for Tomorrow’s Chemical Infrastructure
- (2013) Luc Patiny et al. Journal of Chemical Information and Modeling
- Macrocyclic Drugs and Clinical Candidates: What Can Medicinal Chemists Learn from Their Properties?
- (2013) Fabrizio Giordanetto et al. JOURNAL OF MEDICINAL CHEMISTRY
- Design of orthogonal genetic switches based on a crosstalk map of s, anti- s, and promoters
- (2013) V. A. Rhodius et al. Molecular Systems Biology
- In Vitro Selection of Highly Modified Cyclic Peptides That Act as Tight Binding Inhibitors
- (2012) Yollete V. Guillen Schlippe et al. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
- Ribosomally synthesized and post-translationally modified peptide natural products: overview and recommendations for a universal nomenclature
- (2012) Paul G. Arnison et al. NATURAL PRODUCT REPORTS
- Systematic Mutational Analysis of Peptide Inhibition of the p53–MDM2/MDMX Interactions
- (2010) Chong Li et al. JOURNAL OF MOLECULAR BIOLOGY
- Hydrocarbon double-stapling remedies the proteolytic instability of a lengthy peptide therapeutic
- (2010) G. H. Bird et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- The naturally splitNpuDnaE intein exhibits an extraordinarily high rate in the proteintrans-splicing reaction
- (2009) Joachim Zettler et al. FEBS LETTERS
- Inhibition of HIV Budding by a Genetically Selected Cyclic Peptide Targeting the Gag−TSG101 Interaction
- (2008) Ali Tavassoli et al. ACS Chemical Biology
Create your own webinar
Interested in hosting your own webinar? Check the schedule and propose your idea to the Peeref Content Team.
Create NowAsk a Question. Answer a Question.
Quickly pose questions to the entire community. Debate answers and get clarity on the most important issues facing researchers.
Get Started