#METABOLOMICS WORKBENCH jad2033_20221116_083951 DATATRACK_ID:3577 STUDY_ID:ST002353 ANALYSIS_ID:AN004100 PROJECT_ID:PR001509
VERSION             	1
CREATED_ON             	November 17, 2022, 11:36 am
#PROJECT
PR:PROJECT_TITLE                 	Biomolecular condensates create phospholipid-enriched microenvironments
PR:PROJECT_TYPE                  	Metabolomics of in vitro condensates
PR:PROJECT_SUMMARY               	Proteins and RNA are able to phase separate from the aqueous cellular
PR:PROJECT_SUMMARY               	environment to form sub-cellular compartments called condensates. This process
PR:PROJECT_SUMMARY               	results in a protein-RNA mixture that is chemically distinct from the
PR:PROJECT_SUMMARY               	surrounding aqueous phase. Here we use mass spectrometry to characterize the
PR:PROJECT_SUMMARY               	metabolomes of condensates. To test this, we prepared mixtures of
PR:PROJECT_SUMMARY               	phase-separated proteins and cellular metabolites and identified metabolites
PR:PROJECT_SUMMARY               	enriched in the condensate phase. These proteins included SARS-CoV-2
PR:PROJECT_SUMMARY               	nucleocapsid, as well as low complexity domains of MED1 and HNRNPA1.
PR:INSTITUTE                     	Cornell University
PR:DEPARTMENT                    	Department of Pharmacology
PR:LABORATORY                    	Dr. Samie Jaffrey
PR:LAST_NAME                     	Dumelie
PR:FIRST_NAME                    	Jason
PR:ADDRESS                       	1300 York Ave, LC-524, New York City, NY
PR:EMAIL                         	jdumes98@gmail.com
PR:PHONE                         	6465690174
PR:FUNDING_SOURCE                	This work was supported by the National Institutes of Health grants R35NS111631
PR:FUNDING_SOURCE                	and R01CA186702 (S.R.J.); R01AR076029, R21ES032347 and R21NS118633 (Q.C.); and
PR:FUNDING_SOURCE                	NIH P01 HD067244 and support from the Starr Cancer Consortium I13-0037 (S.S.G.).
PR:PUBLICATIONS                  	Under revision
PR:CONTRIBUTORS                  	Jason G. Dumelie, Qiuying Chen, Dawson Miller, Nabeel Attarwala, Steven S. Gross
PR:CONTRIBUTORS                  	and Samie R. Jaffrey1
#STUDY
ST:STUDY_TITLE                   	Biomolecular condensates create phospholipid-enriched microenvironments (Part 3)
ST:STUDY_SUMMARY                 	Proteins and RNA are able to phase separate from the aqueous cellular
ST:STUDY_SUMMARY                 	environment to form sub-cellular compartments called condensates. This process
ST:STUDY_SUMMARY                 	results in a protein-RNA mixture that is chemically distinct from the
ST:STUDY_SUMMARY                 	surrounding aqueous phase. Here we use mass spectrometry to characterize the
ST:STUDY_SUMMARY                 	metabolomes of condensates. To test this, we prepared mixtures of
ST:STUDY_SUMMARY                 	phase-separated proteins and cellular metabolites and identified metabolites
ST:STUDY_SUMMARY                 	enriched in the condensate phase. These proteins included SARS-CoV-2
ST:STUDY_SUMMARY                 	nucleocapsid, as well as low complexity domains of MED1 and HNRNPA1.
ST:INSTITUTE                     	Cornell University
ST:DEPARTMENT                    	Department of Pharmacology
ST:LABORATORY                    	Dr. Samie Jaffrey
ST:LAST_NAME                     	Dumelie
ST:FIRST_NAME                    	Jason
ST:ADDRESS                       	1300 York Ave, LC-524, New York City, NY
ST:EMAIL                         	jdumes98@gmail.com
ST:STUDY_TYPE                    	Metabolomes of in vitro synthesized condensates
ST:PHONE                         	6465690174
#SUBJECT
SU:SUBJECT_TYPE                  	Synthetic sample
#SUBJECT_SAMPLE_FACTORS:         	SUBJECT(optional)[tab]SAMPLE[tab]FACTORS(NAME:VALUE pairs separated by |)[tab]Raw file names and additional sample data
SUBJECT_SAMPLE_FACTORS           	-	MED1 Library 100 nM Aqueous Sample 1	metabolite_source:100 nM library | protein:MED1 | RNA:150 nM | fraction:aqueous	RAW_FILE_NAME=L1 Top.mzdata.xml;p_L1 Top.mzdata.xml
SUBJECT_SAMPLE_FACTORS           	-	MED1 Library 100 nM Condensate Sample 1	metabolite_source:100 nM library | protein:MED1 | RNA:150 nM | fraction:condensate	RAW_FILE_NAME=L1 Bottom.mzdata.xml;p_L1 Bottom.mzdata.xml
SUBJECT_SAMPLE_FACTORS           	-	MED1 Library 100 nM Input Sample 1	metabolite_source:100 nM library | protein:MED1 | RNA:150 nM | fraction:input	RAW_FILE_NAME=L1 Input.mzdata.xml;p_L1 Input.mzdata.xml
SUBJECT_SAMPLE_FACTORS           	-	MED1 Library 100 nM Aqueous Sample 2	metabolite_source:100 nM library | protein:MED1 | RNA:150 nM | fraction:aqueous	RAW_FILE_NAME=L2 Top.mzdata.xml;p_L2 Top.mzdata.xml
SUBJECT_SAMPLE_FACTORS           	-	MED1 Library 100 nM Condensate Sample 2	metabolite_source:100 nM library | protein:MED1 | RNA:150 nM | fraction:condensate	RAW_FILE_NAME=L2 Bottom.mzdata.xml;p_L2 Bottom.mzdata.xml
SUBJECT_SAMPLE_FACTORS           	-	MED1 Library 100 nM Input Sample 2	metabolite_source:100 nM library | protein:MED1 | RNA:150 nM | fraction:input	RAW_FILE_NAME=L2 Input.mzdata.xml;p_L2 Input.mzdata.xml
SUBJECT_SAMPLE_FACTORS           	-	MED1 Library 100 nM Aqueous Sample 3	metabolite_source:100 nM library | protein:MED1 | RNA:150 nM | fraction:aqueous	RAW_FILE_NAME=L3 Top.mzdata.xml;p_L3 Top.mzdata.xml
SUBJECT_SAMPLE_FACTORS           	-	MED1 Library 100 nM Condensate Sample 3	metabolite_source:100 nM library | protein:MED1 | RNA:150 nM | fraction:condensate	RAW_FILE_NAME=L3 Bottom.mzdata.xml;p_L3 Bottom.mzdata.xml
SUBJECT_SAMPLE_FACTORS           	-	MED1 Library 100 nM Input Sample 3	metabolite_source:100 nM library | protein:MED1 | RNA:150 nM | fraction:input	RAW_FILE_NAME=L3 Input.mzdata.xml;p_L3 Input.mzdata.xml
SUBJECT_SAMPLE_FACTORS           	-	MED1 Library 1 uM Aqueous Sample 1	metabolite_source:1 uM library | protein:MED1 | RNA:150 nM | fraction:aqueous	RAW_FILE_NAME=M1 Top.mzdata.xml;p_M1 Top.mzdata.xml
SUBJECT_SAMPLE_FACTORS           	-	MED1 Library 1 uM Condensate Sample 1	metabolite_source:1 uM library | protein:MED1 | RNA:150 nM | fraction:condensate	RAW_FILE_NAME=M1 Bottom.mzdata.xml;p_M1 Bottom.mzdata.xml
SUBJECT_SAMPLE_FACTORS           	-	MED1 Library 1 uM Input Sample 1	metabolite_source:1 uM library | protein:MED1 | RNA:150 nM | fraction:input	RAW_FILE_NAME=M1 Input.mzdata.xml;p_M1 Input.mzdata.xml
SUBJECT_SAMPLE_FACTORS           	-	MED1 Library 1 uM Aqueous Sample 2	metabolite_source:1 uM library | protein:MED1 | RNA:150 nM | fraction:aqueous	RAW_FILE_NAME=M2 Top.mzdata.xml;p_M2 Top.mzdata.xml
SUBJECT_SAMPLE_FACTORS           	-	MED1 Library 1 uM Condensate Sample 2	metabolite_source:1 uM library | protein:MED1 | RNA:150 nM | fraction:condensate	RAW_FILE_NAME=M2 Bottom.mzdata.xml;p_M2 Bottom.mzdata.xml
SUBJECT_SAMPLE_FACTORS           	-	MED1 Library 1 uM Input Sample 2	metabolite_source:1 uM library | protein:MED1 | RNA:150 nM | fraction:input	RAW_FILE_NAME=M2 Input.mzdata.xml;p_M2 Input.mzdata.xml
SUBJECT_SAMPLE_FACTORS           	-	MED1 Library 1 uM Aqueous Sample 3	metabolite_source:1 uM library | protein:MED1 | RNA:150 nM | fraction:aqueous	RAW_FILE_NAME=M3 Top.mzdata.xml;p_M3 Top.mzdata.xml
SUBJECT_SAMPLE_FACTORS           	-	MED1 Library 1 uM Condensate Sample 3	metabolite_source:1 uM library | protein:MED1 | RNA:150 nM | fraction:condensate	RAW_FILE_NAME=M3 Bottom.mzdata.xml;p_M3 Bottom.mzdata.xml
SUBJECT_SAMPLE_FACTORS           	-	MED1 Library 1 uM Input Sample 3	metabolite_source:1 uM library | protein:MED1 | RNA:150 nM | fraction:input	RAW_FILE_NAME=M3 Input.mzdata.xml;p_M3 Input.mzdata.xml
SUBJECT_SAMPLE_FACTORS           	-	MED1 Library 10 uM Aqueous Sample 1	metabolite_source:10 uM library | protein:MED1 | RNA:150 nM | fraction:aqueous	RAW_FILE_NAME=H1 Top.mzdata.xml;p_H1 Top.mzdata.xml
SUBJECT_SAMPLE_FACTORS           	-	MED1 Library 10 uM Condensate Sample 1	metabolite_source:10 uM library | protein:MED1 | RNA:150 nM | fraction:condensate	RAW_FILE_NAME=H1 Bottom.mzdata.xml;p_H1 Bottom.mzdata.xml
SUBJECT_SAMPLE_FACTORS           	-	MED1 Library 10 uM Input Sample 1	metabolite_source:10 uM library | protein:MED1 | RNA:150 nM | fraction:input	RAW_FILE_NAME=H1 Input.mzdata.xml;p_H1 Input.mzdata.xml
SUBJECT_SAMPLE_FACTORS           	-	MED1 Library 10 uM Aqueous Sample 2	metabolite_source:10 uM library | protein:MED1 | RNA:150 nM | fraction:aqueous	RAW_FILE_NAME=H2 Top.mzdata.xml;p_H2 Top.mzdata.xml
SUBJECT_SAMPLE_FACTORS           	-	MED1 Library 10 uM Condensate Sample 2	metabolite_source:10 uM library | protein:MED1 | RNA:150 nM | fraction:condensate	RAW_FILE_NAME=H2 Bottom.mzdata.xml;p_H2 Bottom.mzdata.xml
SUBJECT_SAMPLE_FACTORS           	-	MED1 Library 10 uM Input Sample 2	metabolite_source:10 uM library | protein:MED1 | RNA:150 nM | fraction:input	RAW_FILE_NAME=H2 Input.mzdata.xml;p_H2 Input.mzdata.xml
SUBJECT_SAMPLE_FACTORS           	-	MED1 Library 10 uM Aqueous Sample 3	metabolite_source:10 uM library | protein:MED1 | RNA:150 nM | fraction:aqueous	RAW_FILE_NAME=H4Top.mzdata.xml;p_H4Top.mzdata.xml
SUBJECT_SAMPLE_FACTORS           	-	MED1 Library 10 uM Condensate Sample 3	metabolite_source:10 uM library | protein:MED1 | RNA:150 nM | fraction:condensate	RAW_FILE_NAME=H4Bottom.mzdata.xml;p_H4Bottom.mzdata.xml
SUBJECT_SAMPLE_FACTORS           	-	MED1 Library 10 uM Input Sample 3	metabolite_source:10 uM library | protein:MED1 | RNA:150 nM | fraction:input	RAW_FILE_NAME=H4Input.mzdata.xml;p_H4Input.mzdata.xml
#COLLECTION
CO:COLLECTION_SUMMARY            	Chemical library to perform condensate metabolomics with a defined set of
CO:COLLECTION_SUMMARY            	lipids. To analyze a defined set of lipids at known concentrations, the
CO:COLLECTION_SUMMARY            	following molecules were purchased: phosphatidylcholine (3:0/3:0)(Cayman
CO:COLLECTION_SUMMARY            	Chemical, 32703), phosphatidylcholine (9:0/9:0)(Cayman Chemical, 10009874),
CO:COLLECTION_SUMMARY            	phosphatidylcholine (12:0/12:0)(Echelon Biosciences, L-1112),
CO:COLLECTION_SUMMARY            	phosphatidylcholine (16:0/16:0)(Echelon Biosciences, L-1116),
CO:COLLECTION_SUMMARY            	phosphatidylcholine (18:0/18:0)(Echelon Biosciences, L-1118),
CO:COLLECTION_SUMMARY            	sn-glycero-3-phosphocholine, lysophosphatidylcholine (16:0)(Echelon Biosciences,
CO:COLLECTION_SUMMARY            	L-1516), palmitic acid (Sigma Aldrich, P5585), phosphatidylethanolamine
CO:COLLECTION_SUMMARY            	(16:0/16:0)(Avanti Polar Lipids, 850705), phosphatidylglycerol
CO:COLLECTION_SUMMARY            	(16:0/16:0)(Avanti Polar Lipids, 840455), phosphatidylinositol
CO:COLLECTION_SUMMARY            	(16:0/16:0)(Echelon Biosciences, P-0016), PIP2 (16:0/16:0)(Echelon Biosciences,
CO:COLLECTION_SUMMARY            	P-4516), phosphatidylserine (16:0/16:0)(Echelon Biosciences, L-3116). These
CO:COLLECTION_SUMMARY            	molecules were first dissolved in an appropriate organic solvent and then either
CO:COLLECTION_SUMMARY            	0.33 pmoles, 3.3 pmoles, or 33 pmoles of each molecule were combined in an
CO:COLLECTION_SUMMARY            	eppendorf tube. The organic solvents were removed using a SpeedVac Concentrator
CO:COLLECTION_SUMMARY            	(Savant, SPD131DDA) at 25oC and the dried chemical libraries were stored at
CO:COLLECTION_SUMMARY            	-80oC. Each tube containing a chemical library was used to perform a single
CO:COLLECTION_SUMMARY            	condensate metabolomics experiment. These libraries were initially re-suspended
CO:COLLECTION_SUMMARY            	in condensate buffer (50 mM NH4HCO3 pH 7.5, 50 mM NaCl, 1 mM DTT). Molecules
CO:COLLECTION_SUMMARY            	that were not fully soluble in condensate buffer were removed by centrifugation
CO:COLLECTION_SUMMARY            	(2x5 min, 16,000 g each), in which only the supernatant was retained. Due to the
CO:COLLECTION_SUMMARY            	lack of crowding agents, phase separation required greater concentrations of
CO:COLLECTION_SUMMARY            	protein and RNA than typically employed for nucleocapsid and MED1 condensate
CO:COLLECTION_SUMMARY            	formation17,32. Purified protein (37.5 μM) was centrifuged (1 min, 1,000 g) to
CO:COLLECTION_SUMMARY            	disrupt any existing condensates and to remove any precipitated proteins.
CO:COLLECTION_SUMMARY            	Purified protein (final concentration, 30 μM) was combined with metabolites
CO:COLLECTION_SUMMARY            	(final concentration, 150 g/l protein equivalent) and then phage lambda RNA
CO:COLLECTION_SUMMARY            	(final concentration, 0.15 μM) in a total volume of 300 µl. An input sample
CO:COLLECTION_SUMMARY            	(10 µl) was saved and then the sample was allowed to incubate for 10 min at
CO:COLLECTION_SUMMARY            	25oC. Condensates were then separated from the aqueous environment by
CO:COLLECTION_SUMMARY            	centrifugation (10 min, 12,500 g, 25oC). The aqueous phase was removed from the
CO:COLLECTION_SUMMARY            	condensate phase and then equal volumes (usually ~ 2 µl) of the aqueous
CO:COLLECTION_SUMMARY            	fraction, condensate fraction and input sample were processed for metabolomics
CO:COLLECTION_SUMMARY            	using identical approaches as described below. First the samples were diluted in
CO:COLLECTION_SUMMARY            	ammonium bicarbonate buffer (50 mM NH4HCO3 pH 7.5) and briefly heated (2 min,
CO:COLLECTION_SUMMARY            	65oC) to disrupt condensates before being added immediately to 4x volume of
CO:COLLECTION_SUMMARY            	ice-cold 100% methanol to precipitate protein and RNA. Protein and RNA were
CO:COLLECTION_SUMMARY            	separated from metabolites by vortexing the samples (2 min), followed by
CO:COLLECTION_SUMMARY            	incubation at -25oC (10 min) and then centrifugation (5 min, 13,000 rpm). The
CO:COLLECTION_SUMMARY            	supernatant was saved and the process was repeated on the pellet two more times
CO:COLLECTION_SUMMARY            	after adding 200 µl of 80% methanol each time to the pellet. The three
CO:COLLECTION_SUMMARY            	supernatants were combined and centrifuged (10 min, 14000 rpm) to remove any
CO:COLLECTION_SUMMARY            	additional macromolecules. The final supernatant was collected and dried using a
CO:COLLECTION_SUMMARY            	SpeedVac Concentrator run at 25oC.
CO:SAMPLE_TYPE                   	Synthetic Mixture
CO:COLLECTION_METHOD             	80% methanol
CO:STORAGE_CONDITIONS            	-80℃
#TREATMENT
TR:TREATMENT_SUMMARY             	Chemical libraries were added with individual molecules at a concentration of
TR:TREATMENT_SUMMARY             	100 nM, 1 uM or 10 uM to the condensate-forming low-complexity domain MED1
TR:TREATMENT_SUMMARY             	tagged with mCherry. Condensates were stimulated with 150 nM RNA. Condensates
TR:TREATMENT_SUMMARY             	were centrifuged to the bottom of a 600 ul tube. Equal fractions from the input
TR:TREATMENT_SUMMARY             	sample, aqueous phase and condensate phases were collected separately.
TR:TREATMENT_SUMMARY             	Metabolites were extracted from each fraction.
#SAMPLEPREP
SP:SAMPLEPREP_SUMMARY            	Metabolites were extracted from each fraction and the input for LC-MS as
SP:SAMPLEPREP_SUMMARY            	follows. First the samples were diluted in ammonium bicarbonate buffer (50 mM
SP:SAMPLEPREP_SUMMARY            	NH4HCO3 pH 7.5) and briefly heated (2 min, 65oC) to disrupt condensates before
SP:SAMPLEPREP_SUMMARY            	being added immediately to 4x volume of ice-cold 100% methanol to precipitate
SP:SAMPLEPREP_SUMMARY            	protein and RNA. Protein and RNA were separated from metabolites by vortexing
SP:SAMPLEPREP_SUMMARY            	the samples (2 min), followed by incubation at -25oC (10 min) and then
SP:SAMPLEPREP_SUMMARY            	centrifugation (5 min, 13,000 rpm). The supernatant was saved and the process
SP:SAMPLEPREP_SUMMARY            	was repeated on the pellet two more times after adding 200 µl of 80% methanol
SP:SAMPLEPREP_SUMMARY            	each time to the pellet. The three supernatants were combined and centrifuged
SP:SAMPLEPREP_SUMMARY            	(10 min, 14000 rpm) to remove any additional macromolecules. The final
SP:SAMPLEPREP_SUMMARY            	supernatant was collected and dried using a SpeedVac Concentrator run at 25oC.
SP:SAMPLEPREP_SUMMARY            	On the day of metabolite analysis, dried-down extracts were reconstituted in 150
SP:SAMPLEPREP_SUMMARY            	µl 70% acetonitrile, at a relative protein concentration of ~ 2 µg/µl, and 4
SP:SAMPLEPREP_SUMMARY            	µl of this reconstituted extract was injected for LC/MS-based untargeted
SP:SAMPLEPREP_SUMMARY            	metabolite profiling.
SP:EXTRACT_STORAGE               	-80℃
#CHROMATOGRAPHY
CH:CHROMATOGRAPHY_SUMMARY        	Tissue extracts were analyzed by LC/MS as described previously, using a platform
CH:CHROMATOGRAPHY_SUMMARY        	comprised of an Agilent Model 1290 Infinity II liquid chromatography system
CH:CHROMATOGRAPHY_SUMMARY        	coupled to an Agilent 6550 iFunnel time-of-flight MS analyzer. Chromatography of
CH:CHROMATOGRAPHY_SUMMARY        	metabolites utilized aqueous normal phase (ANP) chromatography on a Diamond
CH:CHROMATOGRAPHY_SUMMARY        	Hydride column (Microsolv). Mobile phases consisted of: (A) 50% isopropanol,
CH:CHROMATOGRAPHY_SUMMARY        	containing 0.025% acetic acid, and (B) 90% acetonitrile containing 5 mM ammonium
CH:CHROMATOGRAPHY_SUMMARY        	acetate. To eliminate the interference of metal ions on chromatographic peak
CH:CHROMATOGRAPHY_SUMMARY        	integrity and electrospray ionization, EDTA was added to the mobile phase at a
CH:CHROMATOGRAPHY_SUMMARY        	final concentration of 5 µM. The following gradient was applied: 0-1.0 min, 99%
CH:CHROMATOGRAPHY_SUMMARY        	B; 1.0-15.0 min, to 20% B; 15.0 to 29.0, 0% B; 29.1 to 37min, 99% B.
CH:CHROMATOGRAPHY_TYPE           	Normal phase
CH:INSTRUMENT_NAME               	Agilent Model 1290 Infinity II liquid chromatography system
CH:COLUMN_NAME                   	Cogent Diamond Hydride (150 × 2.1 mm, 4um)
CH:SOLVENT_A                     	50% isopropanol, containing 0.025% acetic acid
CH:SOLVENT_B                     	90% acetonitrile containing 5 mM ammonium acetate
#ANALYSIS
AN:ANALYSIS_TYPE                 	MS
#MS
MS:INSTRUMENT_NAME               	Agilent 6550 QTOF
MS:INSTRUMENT_TYPE               	QTOF
MS:MS_TYPE                       	Other
MS:ION_MODE                      	NEGATIVE
MS:MS_COMMENTS                   	LC/MS-based targeted and untargeted metabolite profiling. For targeted analysis,
MS:MS_COMMENTS                   	raw LC/MS data was extracted by MassProfinder 8.0 (Agilent Technologies) using
MS:MS_COMMENTS                   	an in-house annotated personal metabolite database that contains 863 metabolites
MS:MS_COMMENTS                   	(Agilent Technologies). Additionally, molecular feature extraction (MFE) was
MS:MS_COMMENTS                   	performed for untargeted metabolite profiling using MassProfinder 8.0 (Agilent
MS:MS_COMMENTS                   	Technologies). The untargeted molecular features were imported into MassProfiler
MS:MS_COMMENTS                   	Professional 15.1 (MPP, Agilent Technologies) and searched against Metlin
MS:MS_COMMENTS                   	personal metabolite database (PCDL database 8.0), Human Metabolome Database
MS:MS_COMMENTS                   	(HMDB) and an in-house phospholipid database for tentative metabolite ID
MS:MS_COMMENTS                   	assignments, based on monoisotopic neutral mass (< 5 ppm mass accuracy) matches.
MS:MS_COMMENTS                   	Furthermore, a molecular formula generator (MFG) algorithm in MPP was used to
MS:MS_COMMENTS                   	generate and score empirical molecular formulae, based on a weighted
MS:MS_COMMENTS                   	consideration of monoisotopic mass accuracy, isotope abundance ratios, and
MS:MS_COMMENTS                   	spacing between isotope peaks. A tentative compound ID was assigned when PCDL
MS:MS_COMMENTS                   	database and MFG scores concurred for a given candidate molecule. Tentatively
MS:MS_COMMENTS                   	assigned molecules were reextracted using Profinder 8.0 for confirmation of
MS:MS_COMMENTS                   	untargeted results. For phospholipids, assignment of IDs was based on the
MS:MS_COMMENTS                   	defined pattern of neutral loss and head group fragment ions. Metabolites from
MS:MS_COMMENTS                   	targeted and untargeted extraction were combined for further statistical
MS:MS_COMMENTS                   	analysis among groups of input, aqueous and condensate fractions. Metabolites
MS:MS_COMMENTS                   	were removed from our analysis if they had a low ion count or high variation in
MS:MS_COMMENTS                   	input samples. Measurements of metabolite ion counts in input samples should be
MS:MS_COMMENTS                   	replicates across experiments. As such, differences in metabolite ion counts
MS:MS_COMMENTS                   	reflect experimental variability. To determine appropriate cut-offs, we examined
MS:MS_COMMENTS                   	the relationship between metabolite ion counts and their variation across input
MS:MS_COMMENTS                   	sample technical replicates. Metabolites with a median of < 1000 ion
MS:MS_COMMENTS                   	counts/sample tended to have high variation across samples. As a result, these
MS:MS_COMMENTS                   	metabolites were removed. Metabolites were also removed with > 2.5 standard
MS:MS_COMMENTS                   	deviation in log2(ion counts) since the input measurements for these metabolites
MS:MS_COMMENTS                   	were particularly unreliable relative to what was observed for other
MS:MS_COMMENTS                   	metabolites.
#MS_METABOLITE_DATA
MS_METABOLITE_DATA:UNITS	Ion counts
MS_METABOLITE_DATA_START
Samples	MED1 Library 100 nM Condensate Sample 1	MED1 Library 100 nM Condensate Sample 2	MED1 Library 100 nM Condensate Sample 3	MED1 Library 1 uM Condensate Sample 1	MED1 Library 1 uM Condensate Sample 2	MED1 Library 1 uM Condensate Sample 3	MED1 Library 10 uM Condensate Sample 1	MED1 Library 10 uM Condensate Sample 2	MED1 Library 10 uM Condensate Sample 3	MED1 Library 100 nM Input Sample 1	MED1 Library 100 nM Input Sample 2	MED1 Library 100 nM Input Sample 3	MED1 Library 1 uM Input Sample 1	MED1 Library 1 uM Input Sample 2	MED1 Library 1 uM Input Sample 3	MED1 Library 10 uM Input Sample 1	MED1 Library 10 uM Input Sample 2	MED1 Library 10 uM Input Sample 3	MED1 Library 100 nM Aqueous Sample 1	MED1 Library 100 nM Aqueous Sample 2	MED1 Library 100 nM Aqueous Sample 3	MED1 Library 1 uM Aqueous Sample 1	MED1 Library 1 uM Aqueous Sample 2	MED1 Library 1 uM Aqueous Sample 3	MED1 Library 10 uM Aqueous Sample 1	MED1 Library 10 uM Aqueous Sample 2	MED1 Library 10 uM Aqueous Sample 3
Factors	metabolite_source:100 nM library | protein:MED1 | RNA:150 nM | fraction:condensate	metabolite_source:100 nM library | protein:MED1 | RNA:150 nM | fraction:condensate	metabolite_source:100 nM library | protein:MED1 | RNA:150 nM | fraction:condensate	metabolite_source:1 uM library | protein:MED1 | RNA:150 nM | fraction:condensate	metabolite_source:1 uM library | protein:MED1 | RNA:150 nM | fraction:condensate	metabolite_source:1 uM library | protein:MED1 | RNA:150 nM | fraction:condensate	metabolite_source:10 uM library | protein:MED1 | RNA:150 nM | fraction:condensate	metabolite_source:10 uM library | protein:MED1 | RNA:150 nM | fraction:condensate	metabolite_source:10 uM library | protein:MED1 | RNA:150 nM | fraction:condensate	metabolite_source:100 nM library | protein:MED1 | RNA:150 nM | fraction:input	metabolite_source:100 nM library | protein:MED1 | RNA:150 nM | fraction:input	metabolite_source:100 nM library | protein:MED1 | RNA:150 nM | fraction:input	metabolite_source:1 uM library | protein:MED1 | RNA:150 nM | fraction:input	metabolite_source:1 uM library | protein:MED1 | RNA:150 nM | fraction:input	metabolite_source:1 uM library | protein:MED1 | RNA:150 nM | fraction:input	metabolite_source:10 uM library | protein:MED1 | RNA:150 nM | fraction:input	metabolite_source:10 uM library | protein:MED1 | RNA:150 nM | fraction:input	metabolite_source:10 uM library | protein:MED1 | RNA:150 nM | fraction:input	metabolite_source:100 nM library | protein:MED1 | RNA:150 nM | fraction:aqueous	metabolite_source:100 nM library | protein:MED1 | RNA:150 nM | fraction:aqueous	metabolite_source:100 nM library | protein:MED1 | RNA:150 nM | fraction:aqueous	metabolite_source:1 uM library | protein:MED1 | RNA:150 nM | fraction:aqueous	metabolite_source:1 uM library | protein:MED1 | RNA:150 nM | fraction:aqueous	metabolite_source:1 uM library | protein:MED1 | RNA:150 nM | fraction:aqueous	metabolite_source:10 uM library | protein:MED1 | RNA:150 nM | fraction:aqueous	metabolite_source:10 uM library | protein:MED1 | RNA:150 nM | fraction:aqueous	metabolite_source:10 uM library | protein:MED1 | RNA:150 nM | fraction:aqueous
Palmitic acid	6693564.92929273	5494993.84635132	5599044.81421887	7031405.05302905	7983906.70946338	7429736.17232714	4248661.82858826	23501745.2064829	4655878.36239257	6585645.56416187	7424679.71875976	3899044.16138721	5147074.2941438	6537753.67539062	5668873.72906615	5654823.28255933	5407585.03264941	4736340.54955371	1721990.00828482	8208369.77895751	4908535.44942774	4886665.40209497	7072455.95190234	5266215.58012744	6032025.55395434	4901324.15898828	3614481.53658008
PG(16:0/16:0)	2435901.03053126	15862523.8861784	1921368.98833072	7269052.24347144	10713552.6895577	8467777.38671537	12690592.2110736	28268839.2302003	3567491.48828467	11550.9634884643	104616.588147644	1616.67685302734	102543.157090576	333718.043959621	109966.07760357	2951927.01128131	2798376.63380928	523408.615584473	3575.99591552735	6500.07313705445	2552.85514343262	6827.66313659666	8910.49635253907	9159.00347473144	872771.769761949	1098148.95098544	185796.1005961
PI(16:0/16:0)	600080.237881041	474169.917394897	650607.584706543	810807.04700354	1850615.228224	1403043.69323682	3051339.36485167	4336059.86954197	1057917.1677373	135	2729.66770996094	135	135	34095.5964056395	13843.2575778198	742306.991349365	592210.669806639	315628.770388062	135	1999.77688568115	135	135	135	135	42131.8783614502	35084.4988143921	3380.92217285156
PI(45)P2(16:0/16:0)	26419.2188843031	31711.2590063486	7455.39615516669	135245.421676875	144442.933435959	140572.018490839	533350.95619464	594528.428129264	475363.168191987	3480.77297943114	1249.07403182982	1888.40922637939	2935.0774702453	5557.94729766837	6082.01652626034	34649.2142657471	55767.6047261152	27920.2948535919	2069.8720770264	929.394803695667	1149.76533233644	3173.29736991884	542.409973144539	2922.63057281493	21128.9935900818	19464.0623405457	23130.3872657776
PS(16:0/16:0)	1171478.55195834	1003055.57668415	1387078.35885182	963043.248274567	1139715.78876666	921553.795465729	1675004.95612523	1573612.54815022	179971.826880859	2792.46126586914	79650.9921885681	135	135	18605.3902191162	13830.433343811	73393.8294247742	44762.4239234923	28788.6928268433	3941.0306490326	3634.21515136719	1990.24612335205	135	5354.86334579468	10938.7723571777	13892.0876812744	17286.730330658	4891.36015151978
MS_METABOLITE_DATA_END
#METABOLITES
METABOLITES_START
metabolite_name	Mass	RT	KEGG	Formula	PubChem	CAS
Palmitic acid	256.2411	1.45	C00249	C16H32O2	985	57-10-3
PG(16:0/16:0)	722.5083	2.5		C38H75O10P	11846227	200880-41-7
PI(16:0/16:0)	810.5292	2.73		C41H79O13P	24779556	34290-57-8
PI(45)P2(16:0/16:0)	970.4482	9.04		C41H78O19P3		1628353-01-4
PS(16:0/16:0)	735.5096	2.56		C38H73NO10P	46891791	145849-32-7
METABOLITES_END
#END