Imaging mass spectrometry of proteins and peptides: 3d volume reconstruction

Imaging mass spectrometry of proteins and peptides: 3d volume reconstruction

Play all audios:

Loading...

ABSTRACT As large genomic and proteomic datasets are generated from homogenates of various tissues, the need for information on the spatial localization of their encoded products has become


more pressing. Matrix-assisted laser desorption-ionization (MALDI) imaging mass spectrometry (IMS) offers investigators the means with which to unambiguously study peptides and proteins with


molecular specificity, and to determine their distribution in two and three dimensions1,2. In the past few years, several parameters have been optimized for IMS, including sample


preparation, matrix application and instrumental acquisition parameters3,4 (Box 1). These developments have resulted in a high degree of reproducibility in mass accuracy and peak intensities


(Supplementary Fig. 1 online). Recently, we have optimized our protocol to be able to increase the number of molecular species analyzed by collecting two sets of sections, covering one set


of sections with sinapinic acid for optimal detection of proteins and adjacent sections with 2,5-dihydroxybenzoic acid (DHB) matrix for the optimal detection of low-mass species, including


peptides. Approximately 1,000 peaks can be observed in each dataset (Fig. 1). Furthermore, the sections are collected at an equal distance, 200 μm instead of 400–500 μm used previously, thus


enabling the use of virtual _z_-stacks and three-dimensional (3D) volume renderings to investigate differential localization patterns in much smaller brain structures such as the substantia


nigra and the interpeduncular nucleus. Here we present our optimized step-by-step procedure based on previous work in our laboratory2, describing how to make 3D volume reconstructions of


MALDI IMS data, as applied to the rat brain. Access through your institution Buy or subscribe This is a preview of subscription content, access via your institution ACCESS OPTIONS Access


through your institution Subscribe to this journal Receive 12 print issues and online access $259.00 per year only $21.58 per issue Learn more Buy this article * Purchase on SpringerLink *


Instant access to full article PDF Buy now Prices may be subject to local taxes which are calculated during checkout ADDITIONAL ACCESS OPTIONS: * Log in * Learn about institutional


subscriptions * Read our FAQs * Contact customer support SIMILAR CONTENT BEING VIEWED BY OTHERS TOWARD NANOSCALE MOLECULAR MASS SPECTROMETRY IMAGING VIA PHYSICALLY CONSTRAINED MACHINE


LEARNING ON CO-REGISTERED MULTIMODAL DATA Article Open access 26 June 2020 ON-TISSUE DATASET-DEPENDENT MALDI-TIMS-MS2 BIOIMAGING Article Open access 18 November 2023 AUTOMATED ANNOTATION AND


VISUALISATION OF HIGH-RESOLUTION SPATIAL PROTEOMIC MASS SPECTROMETRY IMAGING DATA USING HIT-MAP Article Open access 28 May 2021 REFERENCES * Caprioli, R.M., Farmer, T.B. & Gile, J.


Molecular imaging of biological samples: localization of peptides and proteins using MALDI-TOF MS. _Anal. Chem._ 69, 4751–4760 (1997). Article  CAS  Google Scholar  * Crecelius, A.C. et al.


Three-dimensional visualization of protein expression in mouse brain structures using imaging mass spectrometry. _J. Am. Soc. Mass Spectrom._ 16, 1093–1099 (2005). Article  CAS  Google


Scholar  * Aerni, H.R., Cornett, D.S. & Caprioli, R.M. Automated acoustic matrix deposition for MALDI sample preparation. _Anal. Chem._ 78, 827–834 (2006). Article  CAS  Google Scholar 


* Groseclose, M.R., Andersson, M., Hardesty, W.M. & Caprioli, R.M. Identification of proteins directly from tissue: _in situ_ tryptic digestions coupled with imaging mass spectrometry.


_J. Mass Spectrom._ 42, 254–262 (2007). Article  CAS  Google Scholar  * Reyzer, M.L., Hsieh, Y.S., Ng, K., Korfmacher, W.A. & Caprioli, R.M. Direct analysis of drug candidates in tissue


by matrix-assisted laser desorption/ionization mass spectrometry. _J. Mass Spectrom._ 38, 1081–1092 (2003). Article  CAS  Google Scholar  * Khatib-Shahidi, S., Andersson, M., Herman, J.L.,


Gillespie, T.A. & Caprioli, R.M. Direct molecular analysis of whole-body animal tissue sections by imaging MALDI mass spectrometry. _Anal. Chem._ 78, 6448–6456 (2006). Article  CAS 


Google Scholar  * Hankin, J.A., Barkley, R.M. & Murphy, R.C. Sublimation as a method of matrix application for mass spectrometry imaging. _J. Am. Soc. Mass Spectrom._ 18, 1646–1652


(2007). Article  CAS  Google Scholar  * Schwartz, S.A., Reyzer, M.L. & Caprioli, R.M. Direct tissue analysis using matrix-assisted laser desorption/ionization mass spectrometry:


practical aspects of sample preparation. _J. Mass Spectrom._ 38, 699–708 (2003). Article  CAS  Google Scholar  * Chaurand, P., Norris, J.L., Cornett, D.S., Mobley, J.A. & Caprioli, R.M.


New developments in profiling and imaging of proteins from tissue sections by MALDI mass spectrometry. _J. Proteome Res._ 5, 2889–2900 (2006). Article  CAS  Google Scholar  Download


references ACKNOWLEDGEMENTS We thank D.S. Cornett (Vanderbilt University) for custom data preprocessing software, B. Dawant (Vanderbilt University) for assistance with registration


functions, P. Chaurand and L. Manier (Vanderbilt University) for assistance with MS/MS analyses, J. Morgan (St. Jude Children's Research Hospital, Memphis, Tennessee) for the kind gift


of PEP-19 antibody, and J. Smith (Vanderbilt University) for assistance with using the 3D Amira software. This work was supported by The National Parkinson Foundation Center of Excellence at


Vanderbilt, the National Institute of General Medical Science (GM58008-08), the Department of Defense (W81XWH-05-1-0179) and the National Cancer Institute of the US National Institutes of


Health (CA86243-03). AUTHOR INFORMATION AUTHORS AND AFFILIATIONS * Mass Spectrometry Research Center and Department of Biochemistry, Vanderbilt University Medical Center, 465 21st Avenue


south, Nashville, 37232, Tennessee, USA Malin Andersson, M Reid Groseclose & Richard M Caprioli * Departments of Psychiatry and Pharmacology, Vanderbilt University Medical Center, 465


21st Avenue south, Nashville, 37232, Tennessee, USA Malin Andersson & Ariel Y Deutch Authors * Malin Andersson View author publications You can also search for this author inPubMed 


Google Scholar * M Reid Groseclose View author publications You can also search for this author inPubMed Google Scholar * Ariel Y Deutch View author publications You can also search for this


author inPubMed Google Scholar * Richard M Caprioli View author publications You can also search for this author inPubMed Google Scholar CORRESPONDING AUTHOR Correspondence to Richard M


Caprioli. SUPPLEMENTARY INFORMATION SUPPLEMENTARY TEXT AND FIGURES Supplementary Figures 1–3, Supplementary Methods (PDF 925 kb) SUPPLEMENTARY VIDEO 1 The movie shows the co-registered 3D


volumes of MS imaging data of SP and PEP-19 in the ventral midbrain rotating around its x axis. The movie starts with a frontal view of the midbrain, showing the tissue distribution of SP in


green and PEP-19 in purple. Overlap of peptide and protein distribution is signified by a white appearance. (MOV 1087 kb) SUPPLEMENTARY VIDEO 2 The 3D volumes of MS imaging data of SP and


PEP-19 in the ventral midbrain rotate around the y axis. The movie starts with a frontal view of the midbrain, showing the tissue distribution of SP in green and PEP-19 in purple. Overlap of


peptide and protein distribution is signified by a white appearance. (MOV 961 kb) RIGHTS AND PERMISSIONS Reprints and permissions ABOUT THIS ARTICLE CITE THIS ARTICLE Andersson, M.,


Groseclose, M., Deutch, A. _et al._ Imaging mass spectrometry of proteins and peptides: 3D volume reconstruction. _Nat Methods_ 5, 101–108 (2008). https://doi.org/10.1038/nmeth1145 Download


citation * Issue Date: January 2008 * DOI: https://doi.org/10.1038/nmeth1145 SHARE THIS ARTICLE Anyone you share the following link with will be able to read this content: Get shareable link


Sorry, a shareable link is not currently available for this article. Copy to clipboard Provided by the Springer Nature SharedIt content-sharing initiative