Intracellular and Extracellular Peptidomes of the Model Plant, Physcomitrium patens.

Mass spectrometry Peptidomics Physcomitrium patens Size exclusion chromatography Solid phase extraction

Journal

Methods in molecular biology (Clifton, N.J.)
ISSN: 1940-6029
Titre abrégé: Methods Mol Biol
Pays: United States
ID NLM: 9214969

Informations de publication

Date de publication:
2024
Historique:
medline: 29 3 2024
pubmed: 29 3 2024
entrez: 29 3 2024
Statut: ppublish

Résumé

Here, we report our approach to peptidomic analysis of the plant model Physcomitrium patens. Intracellular and extracellular peptides were extracted under conditions preventing proteolytic digestion by endogenous proteases. The extracts were fractionated on size exclusion columns to isolate intracellular peptides and on reversed-phase cartridges to isolate extracellular peptides, with the isolated peptides subjected to LC-MS/MS analysis. Mass spectrometry data were analyzed for the presence of peptides derived from the known proteins or microproteins encoded by small open reading frames (<100 aa, smORFs) predicted in the moss genome. Experimental details are provided for each step.

Identifiants

pubmed: 38549025
doi: 10.1007/978-1-0716-3646-6_20
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

375-385

Informations de copyright

© 2024. The Author(s), under exclusive license to Springer Science+Business Media, LLC, part of Springer Nature.

Références

Olsson V, Joos L, Zhu S, Gevaert K, Butenko MA, De Smet I (2019) Look closely, the beautiful may be small: precursor-derived peptides in plants. Annu Rev Plant Biol 70:153–186. https://doi.org/10.1146/annurev-arplant-042817-040413
doi: 10.1146/annurev-arplant-042817-040413 pubmed: 30525926
Tavormina P, De Coninck B, Nikonorova N, De Smet I, Cammue BPA (2015) The plant Peptidome: an expanding repertoire of structural features and biological functions. Plant Cell 27:2095–2118. https://doi.org/10.1105/tpc.15.00440
doi: 10.1105/tpc.15.00440 pubmed: 26276833 pmcid: 4568509
Fesenko I, Shabalina SA, Mamaeva A, Knyazev A, Glushkevich A, Lyapina I, Ziganshin R, Kovalchuk S, Kharlampieva D, Lazarev V, Taliansky M, Koonin EV (2021) A vast pool of lineage-specific microproteins encoded by long non-coding RNAs in plants. Nucleic Acids Res 49:10328–10346. https://doi.org/10.1093/nar/gkab816
doi: 10.1093/nar/gkab816 pubmed: 34570232 pmcid: 8501992
Martinez TF, Chu Q, Donaldson C, Tan D, Shokhirev MN, Saghatelian A (2020) Accurate annotation of human protein-coding small open reading frames. Nat Chem Biol 16:458–468. https://doi.org/10.1038/s41589-019-0425-0
doi: 10.1038/s41589-019-0425-0 pubmed: 31819274
Patraquim P, Magny EG, Pueyo JI, Platero AI, Couso JP (2022) Translation and natural selection of micropeptides from long non-canonical RNAs. Nat Commun 13:6515. https://doi.org/10.1038/s41467-022-34094-y
doi: 10.1038/s41467-022-34094-y pubmed: 36316320 pmcid: 9622821
Chen J, Brunner A-D, Cogan JZ, Nuñez JK, Fields AP, Adamson B, Itzhak DN, Li JY, Mann M, Leonetti MD, Weissman JS (2020) Pervasive functional translation of noncanonical human open reading frames. Science 367:1140–1146. https://doi.org/10.1126/science.aay0262
doi: 10.1126/science.aay0262 pubmed: 32139545 pmcid: 7289059
Couso J-P, Patraquim P (2017) Classification and function of small open reading frames. Nat Rev Mol Cell Biol 18:575–589. https://doi.org/10.1038/nrm.2017.58
doi: 10.1038/nrm.2017.58 pubmed: 28698598
Khitun A, Slavoff SA (2019) Proteomic detection and validation of translated small open reading frames. Curr Protoc Chem Biol 11:e77. https://doi.org/10.1002/cpch.77
doi: 10.1002/cpch.77 pubmed: 31750990 pmcid: 6878975
Fesenko IA, Arapidi GP, Skripnikov AY, Alexeev DG, Kostryukova ES, Manolov AI, Altukhov IA, Khazigaleeva RA, Seredina AV, Kovalchuk SI, Ziganshin RH, Zgoda VG, Novikova SE, Semashko TA, Slizhikova DK, Ptushenko VV, Gorbachev AY, Govorun VM, Ivanov VT (2015) Specific pools of endogenous peptides are present in gametophore, protonema, and protoplast cells of the moss Physcomitrella patens. BMC Plant Biol 15:87. https://doi.org/10.1186/s12870-015-0468-7
doi: 10.1186/s12870-015-0468-7 pubmed: 25848929 pmcid: 4365561
Cove DJ, Perroud P-F, Charron AJ, McDaniel SF, Khandelwal A, Quatrano RS (2009) Culturing the moss Physcomitrella patens. Cold Spring Harb Protoc 2009:pdb.prot5136. https://doi.org/10.1101/pdb.prot5136
doi: 10.1101/pdb.prot5136 pubmed: 20147066
Wang X, Qi M, Li J, Ji Z, Hu Y, Bao F, Mahalingam R, He Y (2014) The phosphoproteome in regenerating protoplasts from Physcomitrella patens protonemata shows changes paralleling postembryonic development in higher plants. J Exp Bot 65:2093–2106. https://doi.org/10.1093/jxb/eru082
doi: 10.1093/jxb/eru082 pubmed: 24700621 pmcid: 3991745
Ziganshin R, Arapidi G, Azarkin I, Zaryadieva E, Alexeev D, Govorun V, Ivanov V (2011) New method for peptide desorption from abundant blood proteins for plasma/serum peptidome analyses by mass spectrometry. J Proteome 74:595–606. https://doi.org/10.1016/j.jprot.2011.01.014
doi: 10.1016/j.jprot.2011.01.014
Rappsilber J, Mann M, Ishihama Y (2007) Protocol for micro-purification, enrichment, pre-fractionation and storage of peptides for proteomics using StageTips. Nat Protoc 2:1896–1906. https://doi.org/10.1038/nprot.2007.261
doi: 10.1038/nprot.2007.261 pubmed: 17703201
Slavoff SA, Mitchell AJ, Schwaid AG, Cabili MN, Ma J, Levin JZ, Karger AD, Budnik BA, Rinn JL, Saghatelian A (2013) Peptidomic discovery of short open reading frame–encoded peptides in human cells. Nat Chem Biol 9:59–64. https://doi.org/10.1038/nchembio.1120
doi: 10.1038/nchembio.1120 pubmed: 23160002
Zhu M, Gribskov M (2019) MiPepid: MicroPeptide identification tool using machine learning. BMC Bioinformatics 20:559. https://doi.org/10.1186/s12859-019-3033-9
doi: 10.1186/s12859-019-3033-9 pubmed: 31703551 pmcid: 6842143
Nesvizhskii AI (2014) Proteogenomics: concepts, applications, and computational strategies. Nat Methods 11:1114–1125. https://doi.org/10.1038/nmeth.3144
doi: 10.1038/nmeth.3144 pubmed: 25357241 pmcid: 4392723

Auteurs

Irina Lyapina (I)

Shemyakin-Ovchinnikov Institute of Bioorganic Chemistry RAS, Moscow, Russia.

Igor Fesenko (I)

Shemyakin-Ovchinnikov Institute of Bioorganic Chemistry RAS, Moscow, Russia.

Classifications MeSH