SNARE Modulators and SNARE Mimetic Peptides
The soluble N-ethylmaleimide-sensitive factor (NSF) attachment protein (SNAP) receptor (SNARE) proteins play a central role in most forms of intracellular membrane trafficking, a key process that allows for membrane and biocargo shuffling between multiple compartments within the cell and extracellul...
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2023
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th-mahidol.835012023-06-18T23:43:24Z SNARE Modulators and SNARE Mimetic Peptides Khvotchev M. Mahidol University Biochemistry, Genetics and Molecular Biology The soluble N-ethylmaleimide-sensitive factor (NSF) attachment protein (SNAP) receptor (SNARE) proteins play a central role in most forms of intracellular membrane trafficking, a key process that allows for membrane and biocargo shuffling between multiple compartments within the cell and extracellular environment. The structural organization of SNARE proteins is relatively simple, with several intrinsically disordered and folded elements (e.g., SNARE motif, N-terminal domain, transmembrane region) that interact with other SNAREs, SNARE-regulating proteins and biological membranes. In this review, we discuss recent advances in the development of functional peptides that can modify SNARE-binding interfaces and modulate SNARE function. The ability of the relatively short SNARE motif to assemble spontaneously into stable coiled coil tetrahelical bundles has inspired the development of reduced SNARE-mimetic systems that use peptides for biological membrane fusion and for making large supramolecular protein complexes. We evaluate two such systems, based on peptide-nucleic acids (PNAs) and coiled coil peptides. We also review how the self-assembly of SNARE motifs can be exploited to drive on-demand assembly of complex re-engineered polypeptides. 2023-06-18T16:43:24Z 2023-06-18T16:43:24Z 2022-12-01 Review Biomolecules Vol.12 No.12 (2022) 10.3390/biom12121779 2218273X 36551207 2-s2.0-85144521475 https://repository.li.mahidol.ac.th/handle/123456789/83501 SCOPUS |
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Biochemistry, Genetics and Molecular Biology |
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Biochemistry, Genetics and Molecular Biology Khvotchev M. SNARE Modulators and SNARE Mimetic Peptides |
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The soluble N-ethylmaleimide-sensitive factor (NSF) attachment protein (SNAP) receptor (SNARE) proteins play a central role in most forms of intracellular membrane trafficking, a key process that allows for membrane and biocargo shuffling between multiple compartments within the cell and extracellular environment. The structural organization of SNARE proteins is relatively simple, with several intrinsically disordered and folded elements (e.g., SNARE motif, N-terminal domain, transmembrane region) that interact with other SNAREs, SNARE-regulating proteins and biological membranes. In this review, we discuss recent advances in the development of functional peptides that can modify SNARE-binding interfaces and modulate SNARE function. The ability of the relatively short SNARE motif to assemble spontaneously into stable coiled coil tetrahelical bundles has inspired the development of reduced SNARE-mimetic systems that use peptides for biological membrane fusion and for making large supramolecular protein complexes. We evaluate two such systems, based on peptide-nucleic acids (PNAs) and coiled coil peptides. We also review how the self-assembly of SNARE motifs can be exploited to drive on-demand assembly of complex re-engineered polypeptides. |
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Mahidol University |
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Mahidol University Khvotchev M. |
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Review |
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Khvotchev M. |
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Khvotchev M. |
title |
SNARE Modulators and SNARE Mimetic Peptides |
title_short |
SNARE Modulators and SNARE Mimetic Peptides |
title_full |
SNARE Modulators and SNARE Mimetic Peptides |
title_fullStr |
SNARE Modulators and SNARE Mimetic Peptides |
title_full_unstemmed |
SNARE Modulators and SNARE Mimetic Peptides |
title_sort |
snare modulators and snare mimetic peptides |
publishDate |
2023 |
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https://repository.li.mahidol.ac.th/handle/123456789/83501 |
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1781416501717237760 |