Library Screening, In Vivo Confirmation, and Structural and Bioinformatic Analysis of Pentapeptide Sequences as Substrates for Protein Farnesyltransferase.


Journal

International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791

Informations de publication

Date de publication:
13 May 2024
Historique:
received: 03 02 2024
revised: 07 05 2024
accepted: 08 05 2024
medline: 25 5 2024
pubmed: 25 5 2024
entrez: 25 5 2024
Statut: epublish

Résumé

Protein farnesylation is a post-translational modification where a 15-carbon farnesyl isoprenoid is appended to the C-terminal end of a protein by farnesyltransferase (FTase). This process often causes proteins to associate with the membrane and participate in signal transduction pathways. The most common substrates of FTase are proteins that have C-terminal tetrapeptide CaaX box sequences where the cysteine is the site of modification. However, recent work has shown that five amino acid sequences can also be recognized, including the pentapeptides CMIIM and CSLMQ. In this work, peptide libraries were initially used to systematically vary the residues in those two parental sequences using an assay based on Matrix Assisted Laser Desorption Ionization-Mass Spectrometry (MALDI-MS). In addition, 192 pentapeptide sequences from the human proteome were screened using that assay to discover additional extended CaaaX-box motifs. Selected hits from that screening effort were rescreened using an in vivo yeast reporter protein assay. The X-ray crystal structure of CMIIM bound to FTase was also solved, showing that the C-terminal tripeptide of that sequence interacted with the enzyme in a similar manner as the C-terminal tripeptide of CVVM, suggesting that the tripeptide comprises a common structural element for substrate recognition in both tetrapeptide and pentapeptide sequences. Molecular dynamics simulation of CMIIM bound to FTase further shed light on the molecular interactions involved, showing that a putative catalytically competent Zn(II)-thiolate species was able to form. Bioinformatic predictions of tetrapeptide (CaaX-box) reactivity correlated well with the reactivity of pentapeptides obtained from in vivo analysis, reinforcing the importance of the C-terminal tripeptide motif. This analysis provides a structural framework for understanding the reactivity of extended CaaaX-box motifs and a method that may be useful for predicting the reactivity of additional FTase substrates bearing CaaaX-box sequences.

Identifiants

pubmed: 38791363
pii: ijms25105324
doi: 10.3390/ijms25105324
pii:
doi:

Substances chimiques

Peptide Library 0
Farnesyltranstransferase EC 2.5.1.29
Oligopeptides 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : NIH HHS
ID : GM084152, GM141853, GM132606 and GM132606
Pays : United States

Auteurs

Garrett L Schey (GL)

Department of Medicinal Chemistry, University of Minnesota, Minneapolis, MN 55455, USA.

Emily R Hildebrandt (ER)

Department of Biochemistry and Molecular Biology, University of Georgia, Athens, GA 30602, USA.

You Wang (Y)

Department of Biochemistry, Duke University School of Medicine, Durham, NC 27710, USA.

Safwan Diwan (S)

Department of Chemistry, University of Minnesota, Minneapolis, MN 55455, USA.

Holly A Passetti (HA)

Department of Chemistry, University of Minnesota, Minneapolis, MN 55455, USA.

Gavin W Potts (GW)

Department of Chemistry, University of Minnesota, Minneapolis, MN 55455, USA.

Andrea M Sprague-Getsy (AM)

Department of Chemistry, Syracuse University, Syracuse, NY 13244, USA.

Ethan R Leoni (ER)

Department of Biochemistry and Molecular Biology, University of Georgia, Athens, GA 30602, USA.

Taylor S Kuebler (TS)

Bioinformatics and Computational Biology Graduate Program, University of Minnesota, Minneapolis, MN 55455, USA.

Yuk Y Sham (YY)

Bioinformatics and Computational Biology Graduate Program, University of Minnesota, Minneapolis, MN 55455, USA.
Department of Integrative Biology and Physiology, University of Minnesota, Minneapolis, MN 55455, USA.

James L Hougland (JL)

Department of Chemistry, Syracuse University, Syracuse, NY 13244, USA.
Department of Biology, Syracuse University, Syracuse, NY 13244, USA.
BioInspired Syracuse, Syracuse University, Syracuse, NY 13244, USA.

Lorena S Beese (LS)

Department of Biochemistry, Duke University School of Medicine, Durham, NC 27710, USA.

Walter K Schmidt (WK)

Department of Biochemistry and Molecular Biology, University of Georgia, Athens, GA 30602, USA.

Mark D Distefano (MD)

Department of Medicinal Chemistry, University of Minnesota, Minneapolis, MN 55455, USA.
Department of Chemistry, University of Minnesota, Minneapolis, MN 55455, USA.

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Classifications MeSH