19 research outputs found
Large-scale analysis of peptide sequence variants : the case for high-field asymmetric waveform ion mobility spectrometry
[Image: see text] Large scale analysis of proteins by mass spectrometry is becoming increasingly routine; however, the presence of peptide isomers remains a significant challenge for both identification and quantitation in proteomics. Classes of isomers include sequence inversions, structural isomers, and localization variants. In many cases, liquid chromatography is inadequate for separation of peptide isomers. The resulting tandem mass spectra are composite, containing fragments from multiple precursor ions. The benefits of high-field asymmetric waveform ion mobility spectrometry (FAIMS) for proteomics have been demonstrated by a number of groups, but previously work has focused on extending proteome coverage generally. Here, we present a systematic study of the benefits of FAIMS for a key challenge in proteomics, that of peptide isomers. We have applied FAIMS to the analysis of a phosphopeptide library comprising the sequences GPSGXVpSXAQLX(K/R) and SXPFKXpSPLXFG(K/R), where X = ADEFGLSTVY. The library has defined limits enabling us to make valid conclusions regarding FAIMS performance. The library contains numerous sequence inversions and structural isomers. In addition, there are large numbers of theoretical localization variants, allowing false localization rates to be determined. The FAIMS approach is compared with reversed-phase liquid chromatography and strong cation exchange chromatography. The FAIMS approach identified 35% of the peptide library, whereas LC–MS/MS alone identified 8% and LC–MS/MS with strong cation exchange chromatography prefractionation identified 17.3% of the library
PANC Study (Pancreatitis: A National Cohort Study): national cohort study examining the first 30 days from presentation of acute pancreatitis in the UK
Abstract
Background
Acute pancreatitis is a common, yet complex, emergency surgical presentation. Multiple guidelines exist and management can vary significantly. The aim of this first UK, multicentre, prospective cohort study was to assess the variation in management of acute pancreatitis to guide resource planning and optimize treatment.
Methods
All patients aged greater than or equal to 18 years presenting with acute pancreatitis, as per the Atlanta criteria, from March to April 2021 were eligible for inclusion and followed up for 30 days. Anonymized data were uploaded to a secure electronic database in line with local governance approvals.
Results
A total of 113 hospitals contributed data on 2580 patients, with an equal sex distribution and a mean age of 57 years. The aetiology was gallstones in 50.6 per cent, with idiopathic the next most common (22.4 per cent). In addition to the 7.6 per cent with a diagnosis of chronic pancreatitis, 20.1 per cent of patients had a previous episode of acute pancreatitis. One in 20 patients were classed as having severe pancreatitis, as per the Atlanta criteria. The overall mortality rate was 2.3 per cent at 30 days, but rose to one in three in the severe group. Predictors of death included male sex, increased age, and frailty; previous acute pancreatitis and gallstones as aetiologies were protective. Smoking status and body mass index did not affect death.
Conclusion
Most patients presenting with acute pancreatitis have a mild, self-limiting disease. Rates of patients with idiopathic pancreatitis are high. Recurrent attacks of pancreatitis are common, but are likely to have reduced risk of death on subsequent admissions.
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Large-Scale Analysis of Peptide Sequence Variants: The Case for High-Field Asymmetric Waveform Ion Mobility Spectrometry
Large scale analysis of proteins
by mass spectrometry is becoming
increasingly routine; however, the presence of peptide isomers remains
a significant challenge for both identification and quantitation in
proteomics. Classes of isomers include sequence inversions, structural
isomers, and localization variants. In many cases, liquid chromatography
is inadequate for separation of peptide isomers. The resulting tandem
mass spectra are composite, containing fragments from multiple precursor
ions. The benefits of high-field asymmetric waveform ion mobility
spectrometry (FAIMS) for proteomics have been demonstrated by a number
of groups, but previously work has focused on extending proteome coverage
generally. Here, we present a systematic study of the benefits of
FAIMS for a key challenge in proteomics, that of peptide isomers.
We have applied FAIMS to the analysis of a phosphopeptide library
comprising the sequences GPSGXVpSXAQLXÂ(K/R) and SXPFKXpSPLXFGÂ(K/R),
where X = ADEFGLSTVY. The library has defined limits enabling us to
make valid conclusions regarding FAIMS performance. The library contains
numerous sequence inversions and structural isomers. In addition,
there are large numbers of theoretical localization variants, allowing
false localization rates to be determined. The FAIMS approach is compared
with reversed-phase liquid chromatography and strong cation exchange
chromatography. The FAIMS approach identified 35% of the peptide library,
whereas LC–MS/MS alone identified 8% and LC–MS/MS with
strong cation exchange chromatography prefractionation identified
17.3% of the library
Large-Scale Analysis of Peptide Sequence Variants: The Case for High-Field Asymmetric Waveform Ion Mobility Spectrometry
Large scale analysis of proteins
by mass spectrometry is becoming
increasingly routine; however, the presence of peptide isomers remains
a significant challenge for both identification and quantitation in
proteomics. Classes of isomers include sequence inversions, structural
isomers, and localization variants. In many cases, liquid chromatography
is inadequate for separation of peptide isomers. The resulting tandem
mass spectra are composite, containing fragments from multiple precursor
ions. The benefits of high-field asymmetric waveform ion mobility
spectrometry (FAIMS) for proteomics have been demonstrated by a number
of groups, but previously work has focused on extending proteome coverage
generally. Here, we present a systematic study of the benefits of
FAIMS for a key challenge in proteomics, that of peptide isomers.
We have applied FAIMS to the analysis of a phosphopeptide library
comprising the sequences GPSGXVpSXAQLXÂ(K/R) and SXPFKXpSPLXFGÂ(K/R),
where X = ADEFGLSTVY. The library has defined limits enabling us to
make valid conclusions regarding FAIMS performance. The library contains
numerous sequence inversions and structural isomers. In addition,
there are large numbers of theoretical localization variants, allowing
false localization rates to be determined. The FAIMS approach is compared
with reversed-phase liquid chromatography and strong cation exchange
chromatography. The FAIMS approach identified 35% of the peptide library,
whereas LC–MS/MS alone identified 8% and LC–MS/MS with
strong cation exchange chromatography prefractionation identified
17.3% of the library
“I remember when … ”: The impact of reminiscence therapy on discourse production in older adults with cognitive impairment
Purpose: Positive outcomes following reminiscence therapy have been reported for older adults with mild cognitive impairment and dementia in cognition and quality of life and, in a small number of studies, communication. Despite the close relationship between cognition and language, the impact on communication has received limited attention. This study aimed to investigate whether the spoken discourse of older adults with mild cognitive impairment or dementia could be improved within the genre of nostalgic recounts following group reminiscence therapy, and whether change generalised to everyday discourse. Method: Four females (mean: 87 years, SD: 7.3) who lived in a residential aged care facility and were diagnosed with mild (n = 2) or major (n = 2) neurocognitive impairment were recruited to attend a group reminiscence programme delivered in eight one-hour treatment sessions over four weeks. Multiple baseline samples of discourse were obtained in the week prior to intervention to monitor stability. Macrostructure, rate, informativeness and efficiency of discourse production were measured to identify change within nostalgic recounts and monitor evidence of generalised change in everyday discourse genres. Cognitive performance and quality of life were also monitored. Result: While variability was evident, significant increases in macrostructure and richness of nostalgic recounts were found for two participants, with significant generalisation to everyday discourse. Both participants had diagnoses of mild cognitive impairment. No significant improvements were seen in cognition or quality of life with all participants. Conclusion: This study provides promising evidence for the spoken recall of memories having the potential to improve the communication of people with neurocognitive disorders, with some indication that people with milder impairment may be more amenable to this form of intervention. Nostalgic recounts may provide an explicit context in which speech-language pathologists can facilitate the planning of spoken production in people with cognitive impairment, and influence speaking in everyday contexts.</p
Large-Scale Analysis of Peptide Sequence Variants: The Case for High-Field Asymmetric Waveform Ion Mobility Spectrometry
Vacancy Ordering in SmGe2-x and GdGe2-x (x = 0.33): Structure and Properties of Two Sm3Ge5 Polymorphs and of Gd3Ge5
Severity of Omicron (B.1.1.529) and Delta (B.1.617.2) SARS-CoV-2 infection among hospitalised adults: A prospective cohort study in Bristol, United KingdomResearch in context
Summary: Background: There is an urgent public health need to evaluate disease severity in adults hospitalised with Delta and Omicron SARS-CoV-2 variant infections. However, limited data exist assessing severity of disease in adults hospitalised with Omicron SARS-CoV-2 infections, and to what extent patient-factors, including vaccination, age, frailty and pre-existing disease, affect variant-dependent disease severity. Methods: A prospective cohort study of adults (≥18 years of age) hospitalised with acute lower respiratory tract disease at acute care hospitals in Bristol, UK conducted over 10-months. Delta or Omicron SARS-CoV-2 infection was defined by positive SARS-CoV-2 PCR and variant identification or inferred by dominant circulating variant. We constructed adjusted regression analyses to assess disease severity using three different measures: FiO2 >28% (fraction inspired oxygen), World Health Organization (WHO) outcome score >5 (assessing need for ventilatory support), and hospital length of stay (LOS) >3 days following admission for Omicron or Delta infection. Findings: Independent of other variables, including vaccination, Omicron variant infection in hospitalised adults was associated with lower severity than Delta. Risk reductions were 58%, 67%, and 16% for supplementary oxygen with >28% FiO2 [Relative Risk (RR) = 0.42 (95%CI: 0.34–0.52), P 5 [RR = 0.33 (95%CI: 0.21–0.50), P 3 days [RR = 0.84 (95%CI: 0.76–0.92), P < 0.001]. Younger age and vaccination with two or three doses were also independently associated with lower COVID-19 severity. Interpretation: We provide reassuring evidence that Omicron infection results in less serious adverse outcomes than Delta in hospitalised patients. Despite lower severity relative to Delta, Omicron infection still resulted in substantial patient and public health burden and an increased admission rate of older patients with Omicron which counteracts some of the benefit arising from less severe disease. Funding: AvonCAP is an investigator-led project funded under a collaborative agreement by Pfizer