Mode-of-action of antimicrobial peptides: membrane disruption vs. intracellular mechanisms

AH Benfield, ST Henriques - Frontiers in Medical Technology, 2020 - frontiersin.org
Antimicrobial peptides are an attractive alternative to traditional antibiotics, due to their
physicochemical properties, activity toward a broad spectrum of bacteria, and mode-of …

Macrocycles: lessons from the distant past, recent developments, and future directions

AK Yudin - Chemical science, 2015 - pubs.rsc.org
A noticeable increase in molecular complexity of drug targets has created an unmet need in
the therapeutic agents that are larger than traditional small molecules. Macrocycles, which …

Chemical modifications designed to improve peptide stability: incorporation of non-natural amino acids, pseudo-peptide bonds, and cyclization

L Gentilucci, R De Marco… - Current pharmaceutical …, 2010 - ingentaconnect.com
Functions and properties of native peptides vary from highly specific antibiotics or cytotoxic
antitumor drugs, to hormones, neurotransmitters, immunomodulators, etc. Despite their …

Animal toxins—Nature's evolutionary-refined toolkit for basic research and drug discovery

V Herzig, B Cristofori-Armstrong, MR Israel… - Biochemical …, 2020 - Elsevier
Venomous animals have evolved toxins that interfere with specific components of their
victim's core physiological systems, thereby causing biological dysfunction that aids in prey …

Efficient backbone cyclization of linear peptides by a recombinant asparaginyl endopeptidase

KS Harris, T Durek, Q Kaas, AG Poth, EK Gilding… - Nature …, 2015 - nature.com
Cyclotides are diverse plant backbone cyclized peptides that have attracted interest as
pharmaceutical scaffolds, but fundamentals of their biosynthetic origin remain elusive …

Discovery, synthesis, and structure–activity relationships of conotoxins

KB Akondi, M Muttenthaler, S Dutertre, Q Kaas… - Chemical …, 2014 - ACS Publications
Peptide therapeutics are acclaimed as a promising addition to the pharmaceutical arena,
and they continue to attract interest due to their high potency, bioavailability, and fewer …

Antibodies and venom peptides: new modalities for ion channels

H Wulff, P Christophersen, P Colussi… - Nature Reviews Drug …, 2019 - nature.com
Ion channels play fundamental roles in both excitable and non-excitable tissues and
therefore constitute attractive drug targets for myriad neurological, cardiovascular and …

Making and breaking peptide bonds: protein engineering using sortase

MWL Popp, HL Ploegh - Angewandte Chemie International …, 2011 - Wiley Online Library
Sortases are a class of bacterial enzymes that possess transpeptidase activity. It is their
ability to site‐specifically break a peptide bond and then reform a new bond with an …

The engineering of an orally active conotoxin for the treatment of neuropathic pain

RJ Clark, J Jensen, DJ Craik, ST Nevin… - Angewandte Chemie …, 2010 - elibrary.ru
From killers to curers: Peptides from cone snail venoms are potential therapeutic agents for
the treatment of neuropathic pain. Unfortunately, these peptides suffer from the …

Peptide-based protease inhibitors from plants

R Hellinger, CW Gruber - Drug discovery today, 2019 - Elsevier
Highlights•The human proteasome is the second largest drug target class.•Few prototypic
proteases are standard tools for the discovery of novel inhibitors.•Peptide protease inhibitors …