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1.
Biophys J ; 96(3): 1124-41, 2009 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-19186148

RESUMO

Membrane proteins reside in a structured environment in which some of their residues are accessible to water, some are in contact with alkyl chains of lipid molecules, and some are buried in the protein. Water accessibility of residues may change during folding or function-related structural dynamics. Several techniques based on the combination of pulsed electron paramagnetic resonance (EPR) with site-directed spin labeling can be used to quantify such water accessibility. Accessibility parameters for different residues in major plant light-harvesting complex IIb are determined by electron spin echo envelope modulation spectroscopy in the presence of deuterated water, deuterium contrast in transversal relaxation rates, analysis of longitudinal relaxation rates, and line shape analysis of electron-spin-echo-detected EPR spectra as well as by the conventional techniques of measuring the maximum hyperfine splitting and progressive saturation in continuous-wave EPR. Systematic comparison of these parameters allows for a more detailed characterization of the environment of the spin-labeled residues. These techniques are applicable independently of protein size and require approximately 10-20 nmol of singly spin-labeled protein per sample. For a residue close to the N-terminus, in a domain unresolved in the existing x-ray structures of light-harvesting complex IIb, all methods indicate high water accessibility.


Assuntos
Aminoácidos/química , Complexos de Proteínas Captadores de Luz/química , Complexos de Proteínas Captadores de Luz/metabolismo , Proteínas de Plantas/química , Proteínas de Plantas/metabolismo , Marcadores de Spin , Água/química , Aminoácidos/metabolismo , Soluções Tampão , Cristalografia por Raios X , Detergentes/química , Espectroscopia de Ressonância de Spin Eletrônica , Humanos , Complexos de Proteínas Captadores de Luz/genética , Mutação , Pisum sativum , Proteínas de Plantas/genética , Multimerização Proteica , Estrutura Quaternária de Proteína , Solubilidade , Solventes/química , Temperatura , Água/metabolismo
2.
Chirurg ; 79(3): 249-51, 2008 Mar.
Artigo em Alemão | MEDLINE | ID: mdl-17443304

RESUMO

Cat-scratch disease is an infection by Bartonella henselea and resolves spontaneously. We present a case of untypical Bartonella infection which was misinterpreted by MRI as a soft-tissue sarcoma of the upper arm. The histological findings of an incision biopsy were unspecific, without signs of malignancy. The tumor was excised completely and the final histology, however, showed no evidence of malignant changes. The Bartonella henselae infection could be confirmed by polymerase chain reaction. The untypical presentation of cat-scratch disease should be considered in the differential diagnosis of clinically suspected soft tissue sarcoma.


Assuntos
Braço , Bartonella henselae , Doença da Arranhadura de Gato/diagnóstico , Imageamento por Ressonância Magnética , Dor/etiologia , Sarcoma/diagnóstico , Infecções dos Tecidos Moles/diagnóstico , Neoplasias de Tecidos Moles/diagnóstico , Braço/patologia , Braço/cirurgia , Biópsia , Doença da Arranhadura de Gato/patologia , Doença da Arranhadura de Gato/cirurgia , Diagnóstico Diferencial , Feminino , Humanos , Pessoa de Meia-Idade , Necrose , Sarcoma/patologia , Infecções dos Tecidos Moles/patologia , Infecções dos Tecidos Moles/cirurgia , Neoplasias de Tecidos Moles/patologia , Tela Subcutânea/patologia
3.
Clin Cancer Res ; 6(12): 4803-9, 2000 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-11156238

RESUMO

In this study, the association between telomerase activity and the expression of the human telomerase subunits human telomerase RNA (hTR) and human telomerase reverse transcriptase (hTERT) in paired neoplastic and normal renal tissue samples was investigated. Reverse transcription (RT)-PCR on 20 tumor nephrectomy samples revealed that hTR was constitutively expressed both in cancer and normal tissue samples, independent of the telomerase activity status. Remarkably, using in situ hybridization, the expression levels of hTR were found to be markedly higher in the normal tissue than those in the tumors. Expression of hTERT mRNA by RT-PCR was observed in 90% of the cancer samples and, notably, also in 75% of the corresponding normal renal tissue samples. Because all of the normal tissue samples and some of the tumor samples were shown to be telomerase negative, our findings suggest that hTERT mRNA expression is not sufficient for telomerase enzyme activation. Furthermore, semiquantitative RT-PCR revealed equal or even higher hTERT mRNA expression levels in the telomerase-negative normal samples than in the corresponding cancer samples with telomerase activity, contradicting the assumption that a certain threshold level of hTERT mRNA is required for telomerase activation at least in renal tissue. It seems more likely, that other mechanisms, such as posttranscriptional modification of hTERT or inactivation of telomerase inhibitors, are involved in the acquisition of enzyme activity.


Assuntos
Neoplasias Renais/enzimologia , Rim/enzimologia , RNA , Telomerase/biossíntese , Telomerase/metabolismo , Carcinoma de Células Renais/enzimologia , Proteínas de Ligação a DNA , Humanos , Hibridização In Situ , Rim/patologia , Metástase Linfática , RNA Mensageiro/metabolismo , Reação em Cadeia da Polimerase Via Transcriptase Reversa , Células Tumorais Cultivadas
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