Modes of Social Justice Volume 6, Issue 1 - Full Issue for download

When the theme for this issue of Catalyst was conceived, it was imagined that contributions might present both defenses and critiques of liberal justice, that is, one might say, that these contributions would either promote reformist or revolutionary modes of justice. Instead, all of the submissions took a fairly decisive position of critique of liberal modes of justice, though they are not necessarily in agreement about what constitutes a revolutionary mode of social justice, and they do not always adopt the term \u27revolution\u27 itself as a description of the critique they present and the direction in which they point. Not only did the spirit and letter of the submissions for this issue effectively endorse revolutionary modes of social justice, but these works hit the ground running, with most immediately moving into attempts to describe and help create a strategy of practice for a social justice which could be called revolutionary, and which rather decisively rejects liberalism and in some fundamental ways, conveying in spirit a sense of impatience even with justice as it is conceived and carried out by liberal systems. It is this spirit of the authors of these works and the feeling of eagerness to describe and participate in the effectuation of a revolutionary praxis which they convey, and also on the idea of liberalism as an ideology, on which I focus briefly in this introduction

Idealism and Actualization. Saint-Just in Theory, Practice, and Exigency

Louis-Antoine Léon de Saint-Just (1767-1794) was a revolutionary, a statesman, and a political philosopher, yet it is largely only as a revolutionary that he is remembered. As a political person who occupied these three different but overlapping roles, Saint-Just is ideal as the subject and center of a study of actualization, the taking of political ideals into reality. Saint-Just’s political philosophy was that of an idealist, and yet he, by force of circumstance, ability, and audacity, had the opportunity in his short life to attempt to establish and put into practice his political ideals. In his work as a political person Saint-Just created templates for the understanding of the relationship between political theory and political action. Saint-Just’s political theory is examined in relation to his political action, using the concepts of ‘the natural’, ‘the civil’, ‘the social’ and ‘the political’, concepts which are central in Saint-Just’s political philosophy. Saint-Just’s formulations of these concepts, concepts which have also been central to the history of political philosophy, and his understanding of the relations between these concepts, helps to establish him as a political philosopher of some importance, as does the theory and practice approach to politics which his attempts demanded and which his political life demonstrated. In Saint-Just’s function as political philosopher the thesis finds the theoretical element of politics, which becomes redefined in its interaction with Saint-Just’s other functions as statesman and revolutionary, the latter two of which correspond roughly to practice and exigency. As a theorist who is also a statesman in a context of exigency, or revolution, Saint-Just’s political life is a constantly rearranged juxtaposition of theory, practice, and revolution, albeit one which never loses it essential ties to its philosophical base, even in the hours of greatest emergency. Such dedication to a philosophical base, one which refuses to dispense with political philosophy, demonstrates a new conception of political philosophy for the modern world, fills in elements of a theory of revolution as a phenomenon of both theory and action, and provides a contained case for examination of political philosophy and political action, questioning their disunity

Membrane-Associated RING-CH Proteins Associate with Bap31 and Target CD81 and CD44 to Lysosomes

Membrane-associated RING-CH (MARCH) proteins represent a family of transmembrane ubiquitin ligases modulating intracellular trafficking and turnover of transmembrane protein targets. While homologous proteins encoded by gamma-2 herpesviruses and leporipoxviruses have been studied extensively, limited information is available regarding the physiological targets of cellular MARCH proteins. To identify host cell proteins targeted by the human MARCH-VIII ubiquitin ligase we used stable isotope labeling of amino-acids in cell culture (SILAC) to monitor MARCH-dependent changes in the membrane proteomes of human fibroblasts. Unexpectedly, we observed that MARCH-VIII reduced the surface expression of Bap31, a chaperone that predominantly resides in the endoplasmic reticulum (ER). We demonstrate that Bap31 associates with the transmembrane domains of several MARCH proteins and controls intracellular transport of MARCH proteins. In addition, we observed that MARCH-VIII reduced the surface expression of the hyaluronic acid-receptor CD44 and both MARCH-VIII and MARCH-IV sequestered the tetraspanin CD81 in endo-lysosomal vesicles. Moreover, gene knockdown of MARCH-IV increased surface levels of endogenous CD81 suggesting a constitutive involvement of this family of ubiquitin ligases in the turnover of tetraspanins. Our data thus suggest a role of MARCH-VIII and MARCH-IV in the regulated turnover of CD81 and CD44, two ubiquitously expressed, multifunctional proteins

Editor\u27s Introduction

When the theme for this issue of Catalyst was conceived, it was imagined that contributions might present both defenses and critiques of liberal justice, that is, one might say, that these contributions would either promote reformist or revolutionary modes of justice. Instead, all of the submissions took a fairly decisive position of critique of liberal modes of justice, though they are not necessarily in agreement about what constitutes a revolutionary mode of social justice, and they do not always adopt the term \u27revolution\u27 itself as a description of the critique they present and the direction in which they point

Antigen ligation triggers a conformational change within the constant domain of the αβ T cell receptor

Ligation of the αβ T cell receptor (TCR) by a specific peptide-loaded major histocompatibility complex (pMHC) molecule initiates T cell signaling via the CD3 complex. However, the initial events that link antigen recognition to T cell signal transduction remain unclear. Here we show, via fluorescence-based experiments and structural analyses, that MHC-restricted antigen recognition by the αβ TCR results in a specific conformational change confined to the A-B loop within the α chain of the constant domain (Cα). The apparent affinity constant of this A-B loop movement mirrored that of αβ TCR-pMHC ligation and was observed in two αβ TCRs with distinct pMHC specificities. The Ag-induced A-B loop conformational change could be inhibited by fixing the juxtapositioning of the constant domains and was shown to be reversible upon pMHC disassociation. Notably, the loop movement within the Cα domain, although specific for an agonist pMHC ligand, was not observed with a pMHC antagonist. Moreover, mutagenesis of residues within the A-B loop impaired T cell signaling in an in vitro system of antigen-specific TCR stimulation. Collectively, our findings provide a basis for the earliest molecular events that underlie Ag-induced T cell triggering

Mass-spectrometric identification and relative quantification of N-linked cell surface glycoproteins

Although the classification of cell types often relies on the identification of cell surface proteins as differentiation markers, flow cytometry requires suitable antibodies and currently permits detection of only up to a dozen differentiation markers in a single measurement. We use multiplexed mass-spectrometric identification of several hundred N-linked glycosylation sites specifically from cell surface–exposed glycoproteins to phenotype cells without antibodies in an unbiased fashion and without a priori knowledge. Our cell surface–capturing (CSC) technology, which covalently labels extracellular glycan moieties on live cells, enables the detection and relative quantitative comparison of the cell surface N-glycoproteomes of T and B cells, as well as monitoring changes in the abundance of cell surface N-glycoprotein markers during T-cell activation and the controlled differentiation of embryonic stem cells into the neural lineage. A snapshot view of the cell surface N-glycoprotein will enable detection of panels of N-glycoproteins as potential differentiation markers that are currently not accessible by other means